Yayınlar & Eserler

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

HMZDupFinder: a robust computational approach for detecting intragenic homozygous duplications from exome sequencing data.

Du H., Dardas Z., Jolly A., Grochowski C. M., Jhangiani S. N., Li H., et al.
Nucleic acids research , cilt.52, 2024 (SCI-Expanded) Creative Commons License identifier identifier

Autosomal recessive otospondylo-mega-epiphyseal dysplasia: Comprehensive clinical review of a pediatric cohort

MUTLU H., ELÇİOĞLU H. N., Kiliç E.
Clinical Dysmorphology , cilt.32, sa.4, ss.151-155, 2023 (SCI-Expanded) identifier identifier

Management of acute metabolic crisis in TANGO2 deficiency: A case report

Yllmaz-Gümüş E., ELÇİOĞLU H. N., Genç E., Arlcl Ş., Öztürk G., Yaplcl Ö., et al.
Journal of Pediatric Endocrinology and Metabolism , 2023 (SCI-Expanded) identifier identifier

A novel mutation in the <i>TRIP11</i> gene: Diagnostic approach from relatively common skeletal dysplasias to an extremely rare Odontochondrodysplasia.

Yeter B., Dilruba Aslanger A., Yesil G., Elcioglu N. H.
Journal of clinical research in pediatric endocrinology , cilt.14, ss.475-480, 2022 (SCI-Expanded) identifier identifier identifier identifier

Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia

Panagiotou E. S., Fernandez-Fuentes N., Farraj L. A., McKibbin M., ELÇİOĞLU H. N., Jafri H., et al.
MOLECULAR VISION , cilt.28, ss.57-69, 2022 (SCI-Expanded) identifier identifier identifier

Phenotypic spectrum of BLM- and RMI1-related Bloom syndrome

Goenenc I. I., ELÇİOĞLU H. N., Grijalva C. M., Aras S., Grossmann N., Praulich I., et al.
CLINICAL GENETICS , cilt.101, sa.5-6, ss.559-564, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Disentangling molecular and clinical stratification patterns in beta-galactosidase deficiency

Tebani A., Sudrie-Arnaud B., Dabaj I., Torre S., Domitille L., Snanoudj S., et al.
JOURNAL OF MEDICAL GENETICS , cilt.59, sa.4, ss.377-384, 2022 (SCI-Expanded) identifier identifier identifier

MFSD2A-associated primary microcephaly-Expanding the clinical and mutational spectrum of this ultra-rare disease

Khuller K., Yigit G., Grijalva C. M., Altmueller J., Thiele H., Nurnberg P., et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS , cilt.64, sa.10, 2021 (SCI-Expanded) identifier identifier identifier

High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population

Mitani T., Isikay S., Gezdirici A., Gulec E. Y., Punetha J., Fatih J. M., et al.
AMERICAN JOURNAL OF HUMAN GENETICS , cilt.108, sa.10, ss.1981-2005, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Genome sequencing in families with congenital limb malformations

Elsner J., Mensah M. A., Holtgrewe M., Hertzberg J., Bigoni S., Busche A., et al.
HUMAN GENETICS , cilt.140, sa.8, ss.1229-1239, 2021 (SCI-Expanded) identifier identifier identifier

From cataract to syndrome diagnosis: Revaluation of Warburg-Micro syndrome Type 1 patients

Albayrak H. M., Elcioglu N. H., YETER DOĞAN B., Karaer K.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.185, sa.8, ss.2325-2334, 2021 (SCI-Expanded) identifier identifier identifier

Genotype-phenotype correlations in hereditary multiple exostoses

Akalin I., Kurosawa K., Yeter B., Akbas E., Nishimura G., Wuyts W., et al.
EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.28, sa.SUPPL 1, ss.834, 2020 (SCI-Expanded) identifier

Jeune Syndrome with a novel DYNC2H1 mutation

Elcioglu N. H., Yeter B., Xue J. Y., Wang Z., Guo L., Nishimura G., et al.
EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.28, sa.SUPPL 1, ss.835-836, 2020 (SCI-Expanded) identifier

Development, behaviour and sensory processing in Marshall-Smith syndrome and Malan syndrome: phenotype comparison in two related syndromes.

Mulder P. A., van Balkom I. D. C., Landlust A. M., Priolo M., Menke L. A., Acero I. H., et al.
Journal of intellectual disability research : JIDR , cilt.64, sa.12, ss.956-969, 2020 (SCI-Expanded) identifier identifier identifier

A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with Age

Eltan M., Alavanda C., Yavas Abali Z., Ergenekon P., Yalindag Ozturk N., Sakar M., et al.
CALCIFIED TISSUE INTERNATIONAL , cilt.107, ss.96-103, 2020 (SCI-Expanded) identifier identifier identifier

The genomic and clinical landscape of fetal akinesia

Pergande M., Motameny S., Oezdemir O., Kreutzer M., Wang H., Daimagueler H., et al.
GENETICS IN MEDICINE , cilt.22, sa.3, ss.511-523, 2020 (SCI-Expanded) identifier identifier identifier

TNFRSF11A-Associated Dysosteosclerosis: A Report of the Second Case and Characterization of the Phenotypic Spectrum

Xue J., Wang Z., Shinagawa S., Ohashi H., Otomo N., Elcioglu N. H., et al.
JOURNAL OF BONE AND MINERAL RESEARCH , cilt.34, sa.10, ss.1873-1879, 2019 (SCI-Expanded) identifier identifier identifier

A rare cause of hypophosphatemia: Raine Syndrome

Eltan M., Ata P., Kırkgöz T., Alavanda C., Kaygusuz S. B., Menevse T. S., et al.
HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.384, 2019 (SCI-Expanded) identifier

Molecular characterization of a large group of Mucopolysaccharidosis type IIIC patients reveals the evolutionary history of the disease

Martins C., de Medeiros P. F., Leistner-Segal S., Dridi L., Elcioglu N., Wood J., et al.
HUMAN MUTATION , cilt.40, sa.8, ss.1084-1100, 2019 (SCI-Expanded) identifier identifier identifier

The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance

Pehlivan D., Bayram Y., Gunes N., Akdemir Z. C., Shukla A., Bierhals T., et al.
AMERICAN JOURNAL OF HUMAN GENETICS , cilt.105, sa.1, ss.132-150, 2019 (SCI-Expanded) Creative Commons License identifier identifier identifier

Ptosis as a unique hallmark for autosomal recessive WNT1-associated osteogenesis imperfecta

Nampoothiri S., Guillemyn B., Elcioglu N., Jagadeesh S., Yesodharan D., Suresh B., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.179, sa.6, ss.908-914, 2019 (SCI-Expanded) identifier identifier identifier

The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome

van der Sluijs P. J., Jansen S., Vergano S. A., Adachi-Fukuda M., ALANAY Y., AlKindy A., et al.
GENETICS IN MEDICINE , cilt.21, sa.6, ss.1295-1307, 2019 (SCI-Expanded) Creative Commons License identifier identifier identifier

Does the clinical phenotype of mucolipidosis-III gamma differ from its alpha beta counterpart?: supporting facts in a cohort of 18 patients

Nampoothiri S., Elcioglu N. H., KOCA S. S., Yesodharan D., Chandrababu K. K., Vinod K. V., et al.
CLINICAL DYSMORPHOLOGY , cilt.28, sa.1, ss.7-16, 2019 (SCI-Expanded) identifier identifier identifier

Progressive pseudorheumotoid dysplasia: A presentation of four cases with slow and rapid progression and effects of early rehabilitation program

Giray E., YAĞCI İ., ELÇİOĞLU H. N.
TURKISH JOURNAL OF PHYSICAL MEDICINE AND REHABILITATION , cilt.65, sa.3, ss.290-297, 2019 (SCI-Expanded) identifier identifier identifier

Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice.

Rainger J., van Beusekom E., Ramsay J. K., McKie L., Al-Gazali L., Pallotta R., et al.
PLoS genetics , cilt.14, sa.12, 2018 (SCI-Expanded) Creative Commons License identifier identifier

The oculoauriculofrontonasal syndrome: Further clinical characterization and additional evidence suggesting a nontraditional mode of inheritance

Lehalle D., Altunoglu U., Bruel A., Assoum M., Duffourd Y., Masurel A., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.176, sa.12, ss.2740-2750, 2018 (SCI-Expanded) identifier identifier identifier

Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability

McSherry M., Masih K. E., Elcioglu N. H., Celik P., Balci O., Cengiz F. B., et al.
PLOS ONE , cilt.13, sa.11, 2018 (SCI-Expanded) identifier identifier identifier

Further delineation of Malan syndrome

Priolo M., Schanze D., Tatton-Brown K., Mulder P. A., Tenorio J., Kooblall K., et al.
HUMAN MUTATION , cilt.39, sa.9, ss.1226-1237, 2018 (SCI-Expanded) identifier identifier identifier

Mutations in TOP3A Cause a Bloom Syndrome-like Disorder

Martin C., Sarlos K., Logan C. V., Thakur R. S., Parry D. A., Bizard A. H., et al.
AMERICAN JOURNAL OF HUMAN GENETICS , cilt.103, sa.2, ss.221-231, 2018 (SCI-Expanded) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier identifier

Recessive MYF5 Mutations Cause External Ophthalmoplegia, Rib, and Vertebral Anomalies

Di Gioia S. A., Shaaban S., TÜYSÜZ B., Elcioglu N. H., Chan W., Robson C. D., et al.
AMERICAN JOURNAL OF HUMAN GENETICS , cilt.103, sa.1, ss.115-124, 2018 (SCI-Expanded) identifier identifier identifier

Dysosteosclerosis is also caused by TNFRSF11A mutation

Guo L., Elcioglu N. H., Karalar O. K., Topkar M. O., Wang Z., Sakamoto Y., et al.
JOURNAL OF HUMAN GENETICS , cilt.63, sa.6, ss.769-774, 2018 (SCI-Expanded) identifier identifier identifier

Insights into Mutation Effect in Three Poikiloderma with Neutropenia Patients by Transcript Analysis and Disease Evolution of Reported Patients with the Same Pathogenic Variants

Colombo E. A., Elcioglu N. H., Graziano C., Farinelli P., Di Fede E., Neri I., et al.
JOURNAL OF CLINICAL IMMUNOLOGY , cilt.38, sa.4, ss.494-502, 2018 (SCI-Expanded) Sürdürülebilir Kalkınma identifier

Rothmund-Thomson Syndrome: Insights from New Patients on the Genetic Variability Underpinning Clinical Presentation and Cancer Outcome

Colombo E. A., Locatelli A., Cubells Sanchez L., Romeo S., Elcioglu N. H., Maystadt I., et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES , cilt.19, sa.4, 2018 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Clinico-molecular analysis of eleven patients with Hermansky-Pudlak type 5 syndrome, a mild form of HPS

Michaud V., Lasseaux E., Plaisant C., Verloes A., Perdomo-Trujillo Y., Hamel C., et al.
PIGMENT CELL & MELANOMA RESEARCH , cilt.30, sa.6, ss.563-570, 2017 (SCI-Expanded) identifier identifier identifier

Identification of biallelic EXTL3 mutations in a novel type of spondylo-epi-metaphyseal dysplasia

Guo L., Elcioglu N. H., Mizumoto S., Wang Z., Noyan B., Albayrak H. M., et al.
JOURNAL OF HUMAN GENETICS , cilt.62, sa.8, ss.797-801, 2017 (SCI-Expanded) identifier identifier identifier

Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability

Bramswig N. C., Luedecke H., Hamdan F. F., Altmueller J., Beleggia F., Elcioglu N. H., et al.
HUMAN GENETICS , cilt.136, sa.7, ss.821-834, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis

Bayram Y., White J. J., Elcioglu N., Cho M. T., Zadeh N., Gedikbasi A., et al.
AMERICAN JOURNAL OF HUMAN GENETICS , cilt.101, sa.1, ss.149-156, 2017 (SCI-Expanded) identifier identifier identifier

Novel EYA1 variants causing Branchio-oto-renal syndrome

Klingbeil K. D., Greenland C. M., ArsIan S., Paneque A. L., GÜRKAN H., Ulusal S. D., et al.
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY , cilt.98, ss.59-63, 2017 (SCI-Expanded) identifier identifier identifier

Chondrodysplasia with multiple dislocations: comprehensive study of a series of 30 cases

Ranza E., Huber C., Levin N., Baujat G., Bole-Feysot C., Nitschke P., et al.
CLINICAL GENETICS , cilt.91, sa.6, ss.868-880, 2017 (SCI-Expanded) identifier identifier identifier

Novel and recurrent XYLT1 mutations in two Turkish families with Desbuquois dysplasia, type 2

Guo L., Elcioglu N. H., Iida A., Demirkol Y. K., Aras S., Matsumoto N., et al.
JOURNAL OF HUMAN GENETICS , cilt.62, sa.3, ss.447-451, 2017 (SCI-Expanded) identifier identifier identifier

Mutation Update for Kabuki Syndrome Genes KMT2D and KDM6A and Further Delineation of X-Linked Kabuki Syndrome Subtype 2

Boegershausen N., Gatinois V., Riehmer V., Kayserili H., Becker J., Thoenes M., et al.
HUMAN MUTATION , cilt.37, sa.9, ss.847-864, 2016 (SCI-Expanded) identifier identifier identifier

Molecular etiology of arthrogryposis in multiple families of mostly Turkish origin

Bayram Y., Karaca E., Akdemir Z. C., Yilmaz E. O., Tayfun G. A., AYDIN H., et al.
JOURNAL OF CLINICAL INVESTIGATION , cilt.126, sa.2, ss.762-778, 2016 (SCI-Expanded) identifier identifier identifier

TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfism

Harley M. E., Murina O., Leitch A., Higgs M. R., Bicknell L. S., Yigit G., et al.
NATURE GENETICS , cilt.48, sa.1, ss.36-45, 2016 (SCI-Expanded) Creative Commons License identifier

A THANATOPHORIC DYSPLASIA TYPE I CASE WITH A FGFR3 P.R248C MUTATION AND SURVIVAL BEYOND THE NEONATAL PERIOD

Sahin S., Ograg H., Aslan E. A., Akcan A. B., Turkmen M. K., Moosa S., et al.
GENETIC COUNSELING , cilt.27, sa.4, ss.513-517, 2016 (SCI-Expanded) identifier

A thanatophoric dysplasia type i case with a fgfr3 p.r248c mutation and survival ibeyond the neonatal period

Sahin S., Ograg H., Atasaslan E., Akcan A., Kaynak Turkmen M., Moosa S., et al.
Genetic Counseling , cilt.27, sa.4, ss.513-517, 2016 (SCI-Expanded) identifier identifier

A role for repressive complexes and H3K9 di-methylation in PRDM5-associated brittle cornea syndrome

Porter L. F., Galli G. G., Williamson S., Selley J., Knight D., Elcioglu N., et al.
HUMAN MOLECULAR GENETICS , cilt.24, sa.23, ss.6565-6579, 2015 (SCI-Expanded) identifier identifier identifier

Insights into genotype-phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein-Taybi syndrome patients

Spena S., Milani D., Rusconi D., Negri G., Colapietro P., Elcioglu N., et al.
CLINICAL GENETICS , cilt.88, sa.5, ss.431-440, 2015 (SCI-Expanded) identifier identifier identifier

Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease

Karaca E., Harel T., Pehlivan D., Jhangiani S. N., Gambin T., Akdemir Z. C., et al.
NEURON , cilt.88, sa.3, ss.499-513, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome

Boegershausen N., Tsai I., Pohl E., ŞİMŞEK KİPER P. Ö., Beleggia F., Percin E. F., et al.
JOURNAL OF CLINICAL INVESTIGATION , cilt.125, sa.9, ss.3585-3599, 2015 (SCI-Expanded) identifier identifier identifier

Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome

Atik T., Koparir A., Bademci G., Foster J., Altunoglu U., Mutlu G. Y., et al.
ORPHANET JOURNAL OF RARE DISEASES , cilt.10, 2015 (SCI-Expanded) identifier identifier identifier

Mutations in XRCC4 cause primary microcephaly, short stature and increased genomic instability

Rosin N., Elcioglu N. H., Beleggia F., Isguven P., Altmueller J., Thiele H., et al.
HUMAN MOLECULAR GENETICS , cilt.24, sa.13, ss.3708-3717, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Exome sequencing reveals homozygous TRIM2 mutation in a patient with early onset CMT and bilateral vocal cord paralysis

Pehlivan D., Akdemir Z. C., Karaca E., Bayram Y., Jhangiani S., Yildiz E. P., et al.
HUMAN GENETICS , cilt.134, sa.6, ss.671-673, 2015 (SCI-Expanded) identifier identifier identifier

CRIM1 haploinsufficiency causes defects in eye development in human and mouse

Beleggia F., Li Y., Fan J., Elcioglu N. H., Toker E., Wieland T., et al.
HUMAN MOLECULAR GENETICS , cilt.24, sa.8, ss.2267-2273, 2015 (SCI-Expanded) identifier identifier identifier

The phenotypic and molecular genetic spectrum of Alstrom syndrome in 44 Turkish kindreds and a literature review of Alstrom syndrome in Turkey

Ozanturk A., Marshall J. D., Collin G. B., DÜZENLİ S., Marshall R. P., Candan S., et al.
JOURNAL OF HUMAN GENETICS , cilt.60, sa.1, ss.1-9, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Whole Exome Sequencing Identifies Three Novel Mutations in ANTXR1 in Families with GAPO Syndrome

Bayram Y., Pehlivan D., Karaca E., Gambin T., Jhangiani S. N., Erdin S., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.164, sa.9, ss.2328-2334, 2014 (SCI-Expanded) identifier identifier identifier

Neu-Laxova Syndrome Is a Heterogeneous Metabolic Disorder Caused by Defects in Enzymes of the L-Serine Biosynthesis Pathway

Acuna-Hidalgo R., Schanze D., Kariminejad A., Nordgren A., Kariminejad M. H., Conner P., et al.
AMERICAN JOURNAL OF HUMAN GENETICS , cilt.95, sa.3, ss.285-293, 2014 (SCI-Expanded) identifier identifier identifier

Authors' response: evaluation of choroidal thickness among patients with oculocutaneous albinism

Karabas L., Esen F., ÇELİKER ATABERK H., Elcioglu N., ÇERMAN E., ERASLAN M., et al.
BRITISH JOURNAL OF OPHTHALMOLOGY , cilt.98, sa.8, ss.1135-1136, 2014 (SCI-Expanded) identifier identifier identifier

Decreased subfoveal choroidal thickness and failure of emmetropisation in patients with oculocutaneous albinism

Karabas L., Esen F., ÇELİKER ATABERK H., Elcioglu N., ÇERMAN E., ERASLAN M., et al.
BRITISH JOURNAL OF OPHTHALMOLOGY , cilt.98, sa.8, ss.1087-1090, 2014 (SCI-Expanded) identifier identifier identifier

CNS involvement in OFD1 syndrome: a clinical, molecular, and neuroimaging study

Del Giudice E., Macca M., Imperati F., D'Amico A., Parent P., Pasquier L., et al.
ORPHANET JOURNAL OF RARE DISEASES , cilt.9, 2014 (SCI-Expanded) Creative Commons License identifier

Mutations and polymorphisms in N-acetylgalactosamine-6-sulfate sulfatase gene in Turkish Morquio A patients

Khedhiri S., Chkioua L., Elcioglu N., Laradi S., Miled A.
Pathologie Biologie , cilt.62, sa.1, ss.38-40, 2014 (SCI-Expanded) identifier identifier identifier

Molecular Analysis of Turkish Maroteaux-Lamy Patients and Identification of One Novel Mutation in the Arylsulfatase B (ARSB)Gene

Zanetti A., Onenli-Mungan N., Elcioglu N., Ozbek M. N., KOR D., Lenzini E., et al.
JIMD REPORTS, VOL 14 , cilt.14, ss.1-9, 2014 (SCI-Expanded) Creative Commons License identifier identifier

WERNER SYNDROME: CLINICAL EVALUATION OF TWO CASES AND A NOVEL MUTATION

Mansur A. T., Elcioglu N. H., Demirci G. T.
GENETIC COUNSELING , cilt.25, sa.2, ss.119-127, 2014 (SCI-Expanded) identifier identifier identifier

A comprehensive molecular study on coffin-siris and nicolaides-baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling

Wieczorek D., Boegershausen N., Beleggia F., Steiner-Haldenstaett S., Pohl E., Li Y., et al.
Human Molecular Genetics , cilt.22, sa.25, ss.5121-5135, 2013 (SCI-Expanded) identifier identifier identifier

Mutations in the gene encoding IFT dynein complex component WDR34 cause jeune asphyxiating thoracic dystrophy

Schmidts M., Vodopiutz J., Christou-Savina S., Cortes C. R., McInerney-Leo A. M., Emes R. D., et al.
American Journal of Human Genetics , cilt.93, sa.5, ss.932-944, 2013 (SCI-Expanded) identifier identifier identifier

Mutations in the interleukin receptor IL11RA cause autosomal recessive crouzon-like craniosynostosis

Keupp K., Li Y., Vargel I., Hoischen A., Richardson R., Neveling K., et al.
Molecular Genetics and Genomic Medicine , cilt.1, sa.4, ss.223-237, 2013 (SCI-Expanded) identifier identifier

Clinical and Radiographic Features of the Autosomal Recessive form of Brachyolmia Caused by PAPSS2 Mutations

Iida A., ŞİMŞEK KİPER P. Ö., Mizumoto S., Hoshino T., Elcioglu N., Horemuzova E., et al.
HUMAN MUTATION , cilt.34, sa.10, ss.1381-1386, 2013 (SCI-Expanded) identifier identifier identifier

Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio study

Beaty T. H., Taub M. A., Scott A. F., Murray J. C., Marazita M. L., Schwender H., et al.
HUMAN GENETICS , cilt.132, sa.7, ss.771-781, 2013 (SCI-Expanded) identifier identifier identifier

Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement

Schmidts M., Arts H. H., Bongers E. M. H. F., Yap Z., Oud M. M., Antony D., et al.
JOURNAL OF MEDICAL GENETICS , cilt.50, sa.5, ss.309-323, 2013 (SCI-Expanded) identifier identifier identifier

Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization

Twigg S. R. F., Lloyd D., Jenkins D., Elcioglu N. E., Cooper C. D. O., Al-Sannaa N., et al.
AMERICAN JOURNAL OF HUMAN GENETICS , cilt.91, sa.5, ss.897-905, 2012 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Treacher Collins syndrome: clinical implications for the paediatrician-a new mutation in a severely affected newborn and comparison with three further patients with the same mutation, and review of the literature

Schlump J., Stein A., Hehr U., Karen T., Moeller-Hartmann C., Elcioglu N. H., et al.
EUROPEAN JOURNAL OF PEDIATRICS , cilt.171, sa.11, ss.1611-1618, 2012 (SCI-Expanded) identifier identifier identifier

Association between C677T and A1298C MTHFR gene polymorphism and nonsyndromic orofacial clefts in the Turkish population: a case-parent study

Semic-Jusufagic A., Bircan R., Celebiler O., Erdim M., Akarsu N., Elcioglu N. H.
TURKISH JOURNAL OF PEDIATRICS , cilt.54, sa.6, ss.617-625, 2012 (SCI-Expanded) identifier identifier identifier

The diagnostic challenge of progressive pseudorheumatoid dysplasia (PPRD): A review of clinical features, radiographic features, and WISP3 mutations in 63 affected individuals

Segarra N. G., Mittaz L., Campos-Xavier A. B., Bartels C. F., TÜYSÜZ B., ALANAY Y., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS , cilt.160C, sa.3, ss.217-229, 2012 (SCI-Expanded) identifier identifier identifier

PAPSS2 mutations cause autosomal recessive brachyolmia

Miyake N., Elcioglu N. H., Iida A., Isguven P., Dai J., Murakami N., et al.
JOURNAL OF MEDICAL GENETICS , cilt.49, sa.8, ss.533-538, 2012 (SCI-Expanded) identifier identifier identifier

Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects

Khan K., Logan C. V., McKibbin M., Sheridan E., Elcioglu N. H., Yenice Ö., et al.
HUMAN MOLECULAR GENETICS , cilt.21, sa.4, ss.776-783, 2012 (SCI-Expanded) identifier identifier identifier

Novel C16orf57 mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutations

Colombo E. A., Elcioglu N. H., Yucelten D., Altunay I., Cetincelik U., Teti A., et al.
ORPHANET JOURNAL OF RARE DISEASES , cilt.7, 2012 (SCI-Expanded) identifier identifier identifier

A SHORT RIB POLYDACTYLY SYNDROME OVERLAPPING BOTH LETHAL AND NONLETHAL TYPES

Yigiter A. B., Guducu N., Kavak Z. N., Isci H., Elcioglu N.
GENETIC COUNSELING , cilt.23, sa.2, ss.231-237, 2012 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice

Rainger J., van Beusekom E., Ramsay J. K., McKie L., Al-Gazali L., Pallotta R., et al.
PLOS GENETICS , cilt.7, sa.7, 2011 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Carpenter Syndrome: Extended RAB23 Mutation Spectrum and Analysis of Nonsense-mediated mRNA Decay

Jenkins D., Baynam G., De Catte L., Elcioglu N., Gabbett M. T., Hudgins L., et al.
HUMAN MUTATION , cilt.32, sa.4, 2011 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Mutations in FKBP10 Cause Recessive Osteogenesis Imperfecta and Bruck Syndrome

Kelley B. P., Malfait F., Bonafe L., Baldridge D., Homan E., Symoens S., et al.
JOURNAL OF BONE AND MINERAL RESEARCH , cilt.26, sa.3, ss.666-672, 2011 (SCI-Expanded) identifier identifier identifier

Marie Unna Hereditary Hypotrichosis: A Turkish Family With Loss of Eyebrows and a U2HR Mutation

Mansur A. T., Elcioglu N. H., Redler S., Serdar Z. A., ÇETİNEL Ş., Betz R. C., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.152A, sa.10, ss.2628-2633, 2010 (SCI-Expanded) identifier identifier identifier

LRP4 Mutations Alter Wnt/beta-Catenin Signaling and Cause Limb and Kidney Malformations in Cenani-Lenz Syndrome

Li Y., Pawlik B., Elcioglu N., Aglan M., Kayserili H., Yigit G., et al.
AMERICAN JOURNAL OF HUMAN GENETICS , cilt.86, sa.5, ss.696-706, 2010 (SCI-Expanded) Creative Commons License identifier identifier identifier

A report of a patient with duplication of 7p13 -> pter and deletion of 2p23 -> pter due to a maternal 2p;7p translocation

Turkover B. B., Sayar C., Toksoy G., Elcioglu N.
TURKISH JOURNAL OF PEDIATRICS , cilt.51, sa.2, ss.174-179, 2009 (SCI-Expanded) identifier identifier

Mucopolysaccharidosis Type II: long-term follow-up after bone marrow transplantation

Elcioglu N. H., Vellodi A., Hall C. M.
INTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY AND THERAPEUTICS , cilt.47, 2009 (SCI-Expanded) identifier

A NOVEL LOSS-OF-FUNCTION MUTATION IN THE GNS GENE CAUSES SANFILIPPO SYNDROME TYPE D

Elcioglu N. H., Pawlik B., Colak B., Beck M., Wollnik B.
GENETIC COUNSELING , cilt.20, sa.2, ss.133-139, 2009 (SCI-Expanded) identifier identifier identifier

Mutational Spectrum of the Oral-Facial-Digital Type I Syndrome: A Study on a Large Collection of Patients

Prattichizzo C., Macca M., Novelli V., Giorgio G., Barra A., Franco B.
HUMAN MUTATION , cilt.29, sa.10, ss.1237-1246, 2008 (SCI-Expanded) identifier

Molecular diagnosis of oculocutaneous albinism: new mutations in the OCA1-4 genes and practical aspects

Rooryck C., Morice-Picard F., Elcioglu N. H., Lacombe D., Taieb A., Arveiler B.
PIGMENT CELL & MELANOMA RESEARCH , cilt.21, sa.5, ss.583-587, 2008 (SCI-Expanded) identifier identifier identifier

Adult height in Turkish patients with Turner syndrome without growth hormone treatment

BEREKET A., Turan S., Elcioglu N., Hacihanefioglu S., Memioglu N., Bas F., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.50, sa.5, ss.415-417, 2008 (SCI-Expanded) identifier identifier identifier

Spondylocheiro dysplastic form of the Ehlers-Danlos syndrome - An autosomal-recessive entity caused by mutations in the zinc transporter gene SLC39A13

Giunta C., Elcioglu N. H., Albrecht B., Eich G., Chambaz C., Janecke A. R., et al.
AMERICAN JOURNAL OF HUMAN GENETICS , cilt.82, sa.6, ss.1290-1305, 2008 (SCI-Expanded) identifier identifier identifier

Mucopolysaccharidosis disorders - Abstracts

Elcioglu N., Colak B., Beck M.
ACTA PAEDIATRICA , cilt.97, ss.97, 2008 (SCI-Expanded) identifier

IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy

Beales P. L., Bland E., Tobin J. L., Bacchelli C., Tuysuz B., Hill J., et al.
NATURE GENETICS , cilt.39, sa.6, ss.727-729, 2007 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Colobomatous macrophthalmia with microcornea syndrome maps to the 2p23-p16 region

Elcioglu N. H., Akin B., Toker E., Elcioglu M., Kaya A., Tuncali T., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.143A, sa.12, ss.1308-1312, 2007 (SCI-Expanded) identifier identifier identifier

Novel and recurrent KIND1 mutations in two patients with Kindler syndrome and severe mucosal involvement

Mansur A. T., Elcioglu N. H., Aydingoz I. E., Akkaya A. D., Serdar Z. A., Herz C., et al.
ACTA DERMATO-VENEREOLOGICA , cilt.87, sa.6, ss.563-565, 2007 (SCI-Expanded) identifier identifier identifier

Molecular characterisation of six patients with prolidase deficiency: identification of the first small duplication in the prolidase gene and of a mutation generating symptomatic and asymptomatic outcomes within the same family

Lupi A., Rossi A., Campari E., Pecora F., Lund A. M., Elcioglu N. H., et al.
JOURNAL OF MEDICAL GENETICS , cilt.43, sa.12, 2006 (SCI-Expanded) identifier identifier identifier

Tracheobronchial calcification associated with Keutel syndrome

Oezdemir N., Ersu R., Akalin F., Karadag B. T., Kut A., Karakoc F., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.48, sa.4, ss.357-361, 2006 (SCI-Expanded) identifier identifier identifier

Prenatal diagnosis of Wolf-Hirschhorn syndrome (4p-) in association with congenital diaphragmatic hernia, cystic hygroma and IUGR

Basgul A., Kavak Z., Akman I., Basgul A., Gokaslan H., ELÇİOĞLU H. N.
Clinical and Experimental Obstetrics and Gynecology , cilt.33, sa.2, ss.105-106, 2006 (SCI-Expanded) identifier identifier

When Mucolipidosis III meets Mucolipidosis II: GNPTA gene mutations in 24 patients

Bargal R., Zeigler M., Abu-Libdeh B., Zuri V., Mandel H., Ben Neriah Z., et al.
MOLECULAR GENETICS AND METABOLISM , cilt.88, sa.4, ss.359-363, 2006 (SCI-Expanded) identifier identifier identifier

Prolidase deficiency associated with hemoglobin O trait and microcytic anemia

Aytug A., Ergun T., Ratip S., Elcioglu N., Gultepe M., Mercan E., et al.
INTERNATIONAL JOURNAL OF DERMATOLOGY , cilt.45, sa.7, ss.867-868, 2006 (SCI-Expanded) identifier identifier identifier

BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus

Stoetzel C., Laurier V., Davis E., Muller J., Rix S., Badano J., et al.
NATURE GENETICS , cilt.38, sa.5, ss.521-524, 2006 (SCI-Expanded) identifier identifier identifier

Novel truncating and missense mutations of the KCC3 gene associated with Andermann syndrome

Uyanik G., Elcioglu N., Penzien J., Gross C., Yilmaz Y., Olmez A., et al.
NEUROLOGY , cilt.66, sa.7, ss.1044-1048, 2006 (SCI-Expanded) identifier identifier identifier

Antenatal diagnosis of velocardiofacial syndrome by 3D ultrasonography

Basgul A., Kavak Z., Kotiloglu E., Akman I., Akalin F., Elcioglu N., et al.
JOURNAL OF PERINATAL MEDICINE , cilt.34, sa.2, ss.177-178, 2006 (SCI-Expanded) identifier identifier identifier

Muir-Torre syndrome

Tuncel A., Çelebiler Ö., ELÇİOĞLU H. N.
European Journal of Plastic Surgery , cilt.27, sa.5, ss.241-243, 2004 (SCI-Expanded) identifier

Progeria: A new kind of Laminopathy Report of the First European Symposium on Progeria and creation of EURO-Progeria, a European Consortium on Progeria and related disorders

Brune T., Bonne G., Denecke J., Elcioglu N., Hennekam R. C., Marquardt T., et al.
Pediatric Endocrinology Reviews , cilt.2, sa.1, ss.39-45, 2004 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier

Metatropic dysplasia lethal variants

Hall C., Elcioglu N.
PEDIATRIC RADIOLOGY , cilt.34, sa.1, ss.66-74, 2004 (SCI-Expanded) identifier identifier identifier

Recessive omodysplasia: five new cases and review of the literature

Elcioglu N., Gustavson K., Wilkie A., Yuksel-Apak M., Spranger J.
PEDIATRIC RADIOLOGY , cilt.34, sa.1, ss.75-82, 2004 (SCI-Expanded) identifier identifier identifier

Neonatal Marfan syndrome caused by an exon 25 mutation of the Fibrillin-1 gene

Elcioglu N., Akalin F., Elcioglu M., Comeglio P., Child A.
GENETIC COUNSELING , cilt.15, sa.2, ss.219-225, 2004 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

Short rib-polydactyly syndrome: a case report

Turkmen M., Temocin K., Acar C., Levi E., Karaman C., Inan G., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.45, sa.4, ss.359-362, 2003 (SCI-Expanded) identifier identifier identifier

Colobomatous macrophthalmia with microcornea syndrome: Report of a new pedigree

Toker E., Elcioglu N., Ozcan E., Yenice Ö., Ogut M.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.121A, sa.1, ss.25-30, 2003 (SCI-Expanded) identifier identifier identifier

Alkaptonuria caused by compound heterozygote mutations

Elcioglu N., Aytug A., Muller C., Gurbuz O., Ergun T., Kotiloglu E., et al.
GENETIC COUNSELING , cilt.14, sa.2, ss.207-213, 2003 (SCI-Expanded) identifier identifier identifier

Diagnostic dilemmas in the short rib - Polydactyly syndrome group

Elcioglu N., Hall C.
AMERICAN JOURNAL OF MEDICAL GENETICS , cilt.111, sa.4, ss.392-400, 2002 (SCI-Expanded) identifier identifier identifier

Spondyloepimetaphyseal dysplasia with multiple dislocations (Hall type): three further cases and evidence of autosomal dominant inheritance

Hall C., Elcioglu N., MacDermot K., Offiah A., Winter R.
JOURNAL OF MEDICAL GENETICS , cilt.39, sa.9, ss.666-670, 2002 (SCI-Expanded) identifier identifier identifier

Human Piebaldism: Six Novel Mutations of the Proto-oncogene KIT

Syrris P., Heathcote K., Carrozzo R., Devriendt K., Elcioglu N., Garrett C., et al.
HUMAN MUTATION , cilt.20, sa.3, 2002 (SCI-Expanded) identifier identifier identifier

Dysosteosclerosis: a report of three new cases and evolution of the radiological findings

Elcioglu N., Vellodi A., Hall C.
JOURNAL OF MEDICAL GENETICS , cilt.39, sa.8, ss.603-607, 2002 (SCI-Expanded) identifier identifier identifier

Genetic and mutational analyses of a large multiethnic Bardet-Biedl cohort reveal a minor involvement of BBS6 and delineate the critical intervals of other loci

Beales P., Katsanis N., Lewis R., Ansley S., Elcioglu N., Raza J., et al.
AMERICAN JOURNAL OF HUMAN GENETICS , cilt.68, sa.3, ss.606-616, 2001 (SCI-Expanded) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

Fraser syndrome: Diagnosed in a 50-year-old museum specimen

Elcioglu H. N., Berry A.
AMERICAN JOURNAL OF MEDICAL GENETICS , cilt.94, sa.3, ss.262-264, 2000 (SCI-Expanded) identifier identifier

Pseudo-Torch syndrome: the autosomal recessive syndrome of microcephaly, intracranial calcification and dysmorphism, resembling intrauterine infection.. An additional observation

Elcioglu N., Alper G., Yilmaz Y.
JOURNAL OF MEDICAL GENETICS , cilt.37, 2000 (SCI-Expanded) identifier

A variant of Cenani-Lenz type syndactyly

SEVEN M., Yuksel A., Ozkilic A., Elcioglu N.
GENETIC COUNSELING , cilt.11, sa.1, ss.41-47, 2000 (SCI-Expanded) identifier identifier identifier

Peroxisomal disorders: Clinical and biochemical studies in 15 children and prenatal diagnosis in 7 families

Steinberg S., Elcioglu N., Slade C., Sankaralingam A., Dennis N., Mohammed S., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS , cilt.85, sa.5, ss.502-510, 1999 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey

Beales P., Elcioglu N., Woolf A., Parker D., Flinter F.
JOURNAL OF MEDICAL GENETICS , cilt.36, sa.6, ss.437-446, 1999 (SCI-Expanded) Sürdürülebilir Kalkınma identifier identifier identifier

A Rapp-Hodgkin like syndrome in three sibs: Clinical, dental and dermatoglyphic study

Atasu M., Akesi S., Elcioglu N., Yatmaz P., Ertas E.
CLINICAL DYSMORPHOLOGY , cilt.8, sa.2, ss.101-110, 1999 (SCI-Expanded) identifier identifier identifier

Persistent mullerian duct syndrome - A case report

Erk A., Ozeren S., Ozbay O., Vural B., Elcioglu N.
JOURNAL OF REPRODUCTIVE MEDICINE , cilt.44, sa.2, ss.135-138, 1999 (SCI-Expanded) identifier identifier identifier

Maternal systemic lupus erythematosus and chondrodysplasia punctata in two sibs: phenocopy or coincidence?

Elcioglu N., Hall C.
JOURNAL OF MEDICAL GENETICS , cilt.35, sa.8, ss.690-694, 1998 (SCI-Expanded) Creative Commons License identifier identifier identifier

A distinct form of spondyloepimetaphyseal dysplasia with multiple dislocations

Hall C., Elcioglu N., Shaw D.
JOURNAL OF MEDICAL GENETICS , cilt.35, sa.7, ss.566-572, 1998 (SCI-Expanded) Creative Commons License identifier identifier identifier

A lethal skeletal dysplasia with features of chondrodysplasia punctata and osteogenesis imperfecta: an example of Astley-Kendall dysplasia. Further delineation of a rare genetic disorder

Elcioglu N., Hall C.
JOURNAL OF MEDICAL GENETICS , cilt.35, sa.6, ss.505-507, 1998 (SCI-Expanded) Creative Commons License identifier identifier identifier

Spondylometaphyseal dysplasia Sedaghatian type

Elcioglu N., Hall C.
AMERICAN JOURNAL OF MEDICAL GENETICS , cilt.76, sa.5, ss.410-414, 1998 (SCI-Expanded) identifier identifier identifier

Jeune's asphyxiating thoracic dystrophy of the newborn

Sarimurat N., Elcioglu N., Tekant G., Elicevik M., Yeker D.
EUROPEAN JOURNAL OF PEDIATRIC SURGERY , cilt.8, sa.2, ss.100-101, 1998 (SCI-Expanded) identifier identifier identifier

Temporal aspects in craniometaphyseal dysplasia: Autosomal recessive type

Elcioglu N., Hall C.
AMERICAN JOURNAL OF MEDICAL GENETICS , cilt.76, sa.3, ss.245-251, 1998 (SCI-Expanded) identifier identifier identifier

FISH analysis in patients with clinical diagnosis of Williams syndrome

Elcioglu N., Mackie-Ogilvie C., Daker M., Berry A.
ACTA PAEDIATRICA , cilt.87, sa.1, ss.48-53, 1998 (SCI-Expanded) identifier identifier identifier

Tuberous sclerosis: Clinical evaluation in a family and implications for genetic counseling

Elcioglu N., Karatekin G., Elcioglu M., Nuhoglu A., Cenani A.
GENETIC COUNSELING , cilt.9, sa.2, ss.131-138, 1998 (SCI-Expanded) identifier identifier identifier

Partial trisomy of 15q due to inserted inverted duplication

Elcioglu N., Fear C., Berry A.
CLINICAL GENETICS , cilt.52, sa.6, ss.442-445, 1997 (SCI-Expanded) identifier identifier identifier

Dermatoglyphics in patients with Cenani-Lenz type syndactyly: Studies in a new case

Elcioglu N., Atasu M., Cenani A.
AMERICAN JOURNAL OF MEDICAL GENETICS , cilt.70, sa.4, ss.341-345, 1997 (SCI-Expanded) identifier identifier identifier

Monozygotic twins discordant for the Oculo-oto-radial syndrome (IVIC syndrome)

Elcioglu N., Berry A.
GENETIC COUNSELING , cilt.8, sa.3, ss.201-206, 1997 (SCI-Expanded) identifier identifier identifier

RENAL-FUNCTION DISORDERS IN NEWBORNS WITH PERINATAL ASPHYXIA

ELCIOGLU N., SIRIN A., CAN G., EMRE S., NAYIR A., TANMAN F.
GEBURTSHILFE UND FRAUENHEILKUNDE , cilt.55, sa.3, ss.160-163, 1995 (SCI-Expanded) identifier identifier identifier

THE FREQUENCY OF GENETIC EYE DISEASES IN A GENETIC-COUNSELING CENTER

ELCIOGLU N., ELCIOGLU M., FUHRMANN W.
GENETIC COUNSELING , cilt.6, sa.4, ss.329-342, 1995 (SCI-Expanded) identifier identifier identifier

AN EPIDEMIOLOGIC APPROACH TO ACUTE-RENAL-FAILURE IN CHILDREN

GÖKÇAY E. G., EMRE S., TANMAN F., SIRIN A., ELCIOGLU N., DOLUNAY G.
JOURNAL OF TROPICAL PEDIATRICS , cilt.37, sa.4, ss.191-193, 1991 (SCI-Expanded) identifier identifier identifier

Diğer Dergilerde Yayınlanan Makaleler

Developmental genomics of limb malformations: Allelic series in association with gene dosage effects contribute to the clinical variability

Duan R., Hijazi H., Gulec E. Y., Eker H. K., Costa S. R., Sahin Y., et al.
HUMAN GENETICS AND GENOMICS ADVANCES , cilt.3, sa.4, 2022 (ESCI) identifier identifier identifier

Erken yaşlanma hastalığı Progeria: Hücresel mekanizma ve yeni Tedavi stratejileri

Elçioğlu H. N.
Türkiye Klinikleri Pediatri Dergisi , cilt.1, sa.1, ss.157-164, 2021 (Scopus)

Novel and recurrent COL11A1 and COL2A1 mutations in the Marshall-Stickler syndrome spectrum

Guo L., Elcioglu N. H., Wang Z., Demirkol Y. K., Isguven P., Matsumoto N., et al.
HUMAN GENOME VARIATION , cilt.4, 2017 (ESCI) Creative Commons License identifier

Nijmegen-Breakage Syndrome; Two Siblings Presenting with Different Phenotypes

Kiykim A., AYDINER E., ÖĞÜLÜR İ., BARIŞ S., Ozen A. O., Serifov K., et al.
ASTIM ALLERJI IMMUNOLOJI , cilt.14, sa.2, ss.98-102, 2016 (ESCI) identifier

Successful treatment of pityriasis lichenoides with narrow band ultraviolet B therapy in a patient with KID syndrome a case report

salman A., SEÇKİN GENÇOSMANOĞLU D., YÜCELTEN A. D., elcioğlu n., Richard G., DEMİRKESEN C.
Dermatology Online Journal , cilt.22, sa.5, 2016 (Scopus)

Successful treatment of pityriasis lichenoides chronica with narrow-band ultraviolet B therapy in a patient with keratitis-ichthyosis-deafness syndrome: A case report

SALMAN A., Gencosmanoglu D. S., YÜCELTEN A. D., Elcioglu N., Richard G., Demirkesen C.
Dermatology Online Journal , cilt.22, sa.5, 2016 (Scopus) identifier identifier

Consanguineous Marriage in Turkey and its Meaning for Genetic Counselling Verwandtenehen in der Türkei und ihre Bedeutung für die genetische Praxis

Elçioglu N., Cenani A.
Munchener Medizinische Wochenschrift , cilt.139, sa.48, ss.715-718, 1997 (Scopus) identifier

A survey amongst German human genetic specialists about the situation of genetic counselling of Turkish patients in Germany EINE UMFRAGE BEI DEUTSCHEN HUMANGENETIKERN ZUR SITUATION DER GENETISCHEN BERATUNG VON TURKISCHEN RATSUCHENDEN IN DEUTSCHLAND

Elcioglu N.
Medizinische Genetik , cilt.7, sa.4, ss.442-447, 1995 (Scopus) identifier

Renal function in full-term newborn following neonatal asphyxia

Elcioglu N., Sirin A., Can G., Tanman F., Emre S., Nayir A.
Istanbul Tip Fakultesi Mecmuasi , cilt.55, sa.3, ss.437-443, 1992 (Scopus) identifier

Our experience with the patients of complete and corrected transposition of great arteries

Elcioglu N., Eker R., Sarioglu T., Aytac A., Barlas C., Cantez T.
Istanbul Tip Fakultesi Mecmuasi , cilt.53, sa.3, ss.15-20, 1990 (Scopus) identifier

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Famililal Chilblain Lupus preading to two countries, affecting three Generations with variable phenotypic expressivity. Oral presentation [OP-45] 03.2022 Istanbul, Turkey

SERDAR Z., ELÇİOĞLU H. N., ALTAN FERHATOĞLU Z., Serdar İ.
7.INDERCOS International Dermatology and Cosmetology Congress, İstanbul, Türkiye, 9 - 12 Mart 2022

Çocuk Genetik Polikliniğinde Değerlendirilen Osteogenezis İmperfekta Olgularının Klinik ve Genomik Özellikleri: Tek Merkez Deneyimi S110

KARALAR PEKUZ Ö. K., ELÇİOĞLU H. N.
3.Uluslararası Behçet Uz Çocuk Kongresi, 23-25 Eylül 2021 İzmir, İzmir, Türkiye, 23 - 25 Eylül 2021, ss.182-183

Katepsin C Gen Mutasyonuyla İlişkili Agresif Periodontitisli İki Kardeşin Ağız İçi Bulguları

GÜNGÖRMEK H. S., HAZNEDAROĞLU E., MENTEŞ A. R., ÖZEMRİ SAĞ Ş., ZEYBEK S., TEMEL Ş. G., et al.
1. Bursa Uluslararası Katılımlı Genetik Günleri: Dermatogenetik Sempozyumu, Bursa, Türkiye, 9 - 11 Ocak 2020

DASS Sendromlu Çocuk Hastanın Oro-dental Bulguları

Karaman G. E., AKYÜZ S. H., ELÇİOĞLU H. N., MENTEŞ A. R.
26. Uluslararası Türk Pedodonti Derneği Kongresi, 10 - 13 Ekim 2019

Hipokondroplazi: FGFR3 mutasyonlu 4 Olgu Sunumu

Aliyeva S., Tabakçı B., AKALIN İ., ELÇİOĞLU H. N.
4. Çocuk Genetik Kongresi, Türkiye, 25 - 27 Eylül 2019

A novel intermediate type osteopetrosis associated with a new homozygous CLCN7 mutation

AKALIN İ., Xue J., Doğan B., Yılmaz S., Long G., ASLAN E., et al.
14th International Skeletal Dysplasia Society Meeting, 11 - 14 Eylül 2019, cilt.1, ss.91

A rare cause of hypophosphatemia: Raine Syndrome

ELTAN M., ATA P., KIRKGÖZ T., ALAVANDA C., KAYGUSUZ S. B., SEVEN M. T., et al.
European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, VİYANA, Avusturya, 19 - 21 Eylül 2019, cilt.91

Exome sequencing reveals novel candidate genes and potential oligogenic inheritance in patients with the complex trait arthrogryposis

Pehlivan D., Bayram Y., Akdemir Z. C., Fatih J., Gibbs R., Posey J., et al.
71st Annual Meeting of the American-Academy-of-Neurology (AAN), Pennsylvania, Amerika Birleşik Devletleri, 4 - 10 Mayıs 2019, cilt.92 identifier

Molecular characterization and haplotype analysis in a large group of Mucopolysaccharidosis type IIIC (MPS IIIC) patients reveal the evolutionary history of the disease

Martins C., Frassinetti de Medeiros P., Leistner-Segal S., Elcioglu N., Behnam M., Lacerda L., et al.
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.778 identifier

Çocukluk Çağında Diyabetin Nadir bir Nedeni: Glukokinaz Mutasyonu (MODY 2)

İşgüven Ş. P., Bingöl Aydın D., Dönmez Ersavaş D., Elçioğlu H. N.
62. Türkiye Milli Pediatri kongresi-2. Kosova -Türkiye Pediatri kongresi, Antalya, Türkiye, 15 - 19 Kasım 2017 Sürdürülebilir Kalkınma

Whole exome sequencing reveals potetial oligenic inheritance and candidate novel genes in patients with arthrogryposis

BAYRAM Y., PEHLİVAN D., TÜYSÜZ B., ELÇİOĞLU H. N.
ASHG 67th Annual meeting, 17 Ekim 2017 - 21 Ocak 2018

Whole exome sequencing reveals potential oligogenic inheritance andcandidate novel genes in patients with arthrogryposis

BAYRAM Y., ULUDAĞ ALKAYA D., pehlivan d., Gezdirici A., SILAN F., ÖZDEMİR Ö., et al.
American Society of Human Genetics 67thAnnual Meeting, 17 - 21 Ekim 2017

Molecular characterization and haplotype analysis in a large group of Mucoplysachrarisosis type IIC (MPS IIIC) patients reveal the evolutionary hystory of the disease

Martins C., Segal S L., Pshezhetsky A., ELÇİOĞLU H. N.
ESHG 2017 Kopenhagen, 27 - 30 Mayıs 2017

Mutation spectrum and haplotype study of mucopolysaccharidosis type IIIC patients reveal possible migration events and founder effects of HGSNAT mutations

Martins C., de Medeiros P. F., Leistner-Segal S., Elcioglu N., Behnam M., Lacerda L., et al.
13th Annual Research Meeting on We're Organizing Research for Lysosomal Diseases (WORLD), California, Amerika Birleşik Devletleri, 13 - 17 Şubat 2017, cilt.120 identifier

A novel homozygous IFT122 p I460N c 1379T A mutation inSensenbrenner syndrome a rare disorder within two cousins

AKALIN İ., ELÇİOĞLU H. N., CANDAN C., YILMAZ S., Yücetürk B.
ESHG kongresi, 21 - 24 Mayıs 2016

RASopaties: two case reports

DEMİRKOL KENDİR Y., Alp Ünkar Z., ÖZDEMİR H., BİLGEN H. S., ELÇİOĞLU H. N.
1st Congress of the European The Young Paediatricians’ Association, İstanbul, Türkiye, 4 - 06 Aralık 2015

RASopaties two case reports

Demirkol Y., Alp Z., BİLGEN H. S., ELÇİOĞLU H. N.
1. EURYPA congress, İstanbul, Türkiye, 4 - 06 Aralık 2015

Double aneuploidy: Down – Klinefelter Syndrome

ALP UNKAR Z., KENDİR DEMİRKOL Y., MEMİŞOĞLU A., ELÇİOĞLU H. N., ÖZEK E.
1st Congress Of The European Young Paediatricians’ Association (EURYPA), 4 - 06 Aralık 2015

Molecular etiology of arthrogryposis in a cohort of families of Turkish origin Y Bayram 1 E Karaca 1 Z Coban Akdemir 1 H Aydin 2 A Gezdirici 3 D Torun 4 S Tug Bozdogan 5 S Isikay 6 M M Atik 1 T Gambin 1 A Karaman 7 D Pehlivan 1 H Aslan 8 O Ozalp Yuregir 9 S N Jhangiani 10 E Boerwinkle 10 11 R A Gibbs 10 N Elcioglu 12 B Tuysuz 13 J R Lupski

BAYRAM Y., Karaca E., Çoban A. Z., Aydın H., Gezdirici A., TORUN D., et al.
Congress ASHG 2015, 6 - 10 Ekim 2015

The Skeletal Changes in Hurler s Syndrome afterBone Marrow Transplantation

ELÇİOĞLU H. N.
12thINTERNATIONAL SKELETAL DYSPLASIA SOCIETY MEETING, 29 Temmuz - 01 Ağustos 2015

Mucolipidosis III Gamma Patients

ELÇİOĞLU H. N.
12thINTERNATIONAL SKELETAL DYSPLASIA SOCIETY MEETING, 29 Temmuz - 01 Ağustos 2015

CLINICAL AND MOLECULAR STUDY OF A SERIES OF 31 PATIENTS WITH CHONDRODYSPLASIA WITH MULTIPLE DISLOCATIONS

Ranza E., Huber C., Levin N., Baujat G., ALANAY Y., Al Gazali L., et al.
12thINTERNATIONAL SKELETAL DYSPLASIA SOCIETY MEETING’, 29 Temmuz - 01 Ağustos 2015

A molecular network surrounding dysregulated H3K9 di methylation in PRDM5 associated disease

Porter L., Gall G., Williamson S., Selley J., Knight D., ELÇİOĞLU H. N., et al.
European Human GeneticsConference 2015, 6 - 09 Haziran 2015

Spotlight on the pathogenesis of Kabuki syndrome

Bögershausen N., Tsai I., Pohl E., ŞİMŞEK KİPER P. Ö., Beleggia F., Percin F., et al.
European Human GeneticsConference 2015, 6 - 09 Haziran 2015

Brakio Okülo Fasiyel Sendromlu Bir Olguda Axenfeld Rieger Anomalisi

AKAY TAYFUN G., ELÇİOĞLU H. N., ÇERMAN E., ÖZARSLAN ÖZCAN D., ERASLAN M.
1. MARMARA PEDİATRİ KONGRESİ, Türkiye, 17 - 19 Ocak 2014

Brankio Oküler Fasiyel Sendromlu Bir Olguda Göz Bulguları

ÇERMAN E., ÖZARSLAN ÖZCAN D., ERASLAN M., AKKAYA TAYFUN G., ELÇİOĞLU H. N.
47. TÜRK OFTALMOLOJİ DERNEĞİ ULUSAL KONGRESİ, Türkiye, 6 - 10 Kasım 2013

Succesful treatment of Pityriasis Lichenoides Chronica with Narrow-Band Ultraviolet B Therapy in a Patient with Keratitis-Ichthyosis-Deafness Syndrome: A Case Report

SALMAN A., SEÇKİN GENÇOSMANOĞLU D., YÜCELTEN A. D., ELÇİOĞLU H. N., RICHARD G., DEMİRKESEN C.
11th European Society for Pediatric Dermatology Congress, 16 - 19 Mayıs 2012

Phenotype, Genetics and Natural History in 146 Patients with SEPN1-Related Myopathy: On the Way to Therapeutic Trials in a Rare Disorder

Malfatti E., Martinez V. G., Von der Hagen M., Chabalier D., Quijano-Roy S., David O., et al.
63rd AAN Annual Meeting, Hawaii, Amerika Birleşik Devletleri, 9 - 16 Nisan 2011, cilt.76 identifier

Werner Syndrome and Rothmund-Thomson syndrome: are they some cases with overlapping phenotypes resembling both disease?

Elcioglu N. H., Mansur A. T., Aslan-Kayiran M.
British Human Genetics Conference, York, Sierra Leone, 15 - 17 Eylül 2008, cilt.45 identifier

POMPE DISEASE AND EXPERIENCE WITH PRENATAL DIAGNOSIS

Elcioglu N., Akalin F., van der Luijt R. B.
5th Symposium on Lysosomal Storage Disorders, Paris, Fransa, 10 - 12 Nisan 2008, cilt.30 identifier

SEPN-related myopathy: an emerging entity phenotypical and molecular analysis of 80 cases

Gonzalez V., Quijano-Roy S., Parain K., Bonnemann C., Bushby K., Castiglioni C., et al.
10th International Congress of the World-Muscle-Society, Iguassu Falls, Brezilya, 28 Eylül - 10 Ekim 2005, cilt.15, ss.715 identifier

Spondylothoracic dysplasia (Jarcho-Levin syndrome) and Spondylocostal dysostosis, the confusing vertebral malsegmentation syndromes. Report of six cases

Semic A., Elcioglu N., Yalcin S., Biren T.
European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics, Strasbourg, Fransa, 25 - 28 Mayıs 2002, cilt.10, ss.113 identifier

Isolated fetal choroid plexus cysts and association with chromosome anomalies

Sayar C., Sahinoglu Z., Uludogan M., Turkover B., Elcioglu N.
European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics, Strasbourg, Fransa, 25 - 28 Mayıs 2002, cilt.10, ss.276-277 identifier

Kitap & Kitap Bölümleri

DNA tamir hastalıkları

ELÇİOĞLU H. N., ARAS S.
İzmir Behçet Uz Çocuk Hastanesi Pediatri Kitabı, Editör Behzat Özkan, Derya Erçal, Editör, Nobel Kitapevi, Ankara, ss.222-225, 2022

Erken yaşlanma hastalığı progeria: Hücresel mekanizma ve yeni tedavi stratejileri

ELÇİOĞLU H. N.
Çocuk Genetik Uygulamalarında Sık Görülen Hastalıkların Takip ve Tedavisi, Ercan Mıhçı, Editör, Türkiye Klinikleri Pediatri Dergisi, Ankara, ss.157-164, 2021

Malformasyon Sendromlarına Yaklaşım

Elçioğlu H. N.
NEONATOLOJİ 3. baskı, Türkan Dağoğlu,Fahri Ovalı, Editör, Nobel Tıp Kitapevi, İstanbul, ss.361-388, 2017

Bağ Doku Hastalıkları

Elçioğlu H. N.
TİBBİ GENETİK ve KLİNİK UYGULAMALARI, Munis Dündar, Editör, Hipokrat, Kayseri, ss.817-834, 2016

Metrikler

Yayın

184

Atıf (WoS)

4101

H-İndeks (WoS)

33

Atıf (Scopus)

4832

H-İndeks (Scopus)

34

Proje

1

Tez Danışmanlığı

14

Açık Erişim

16
BM Sürdürülebilir Kalkınma Amaçları