Yayınlar & Eserler

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Human CRY1 variants associate with attention deficit/hyperactivity disorder

JOURNAL OF CLINICAL INVESTIGATION, cilt.130, sa.7, ss.3885-3900, 2020 (SCI İndekslerine Giren Dergi) Creative Commons License identifier identifier identifier

Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutation

DIAGNOSTIC AND INTERVENTIONAL RADIOLOGY, cilt.24, sa.6, ss.392-401, 2018 (SCI İndekslerine Giren Dergi) Creative Commons License identifier identifier identifier

Genomic landscape of the Greater Middle East

NATURE GENETICS, cilt.48, sa.9, ss.978-979, 2016 (SCI İndekslerine Giren Dergi) Creative Commons License identifier identifier

Reply to Tzoulis et al.: Genetic and clinical heterogeneity of essential tremor

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, cilt.112, sa.18, 2015 (SCI İndekslerine Giren Dergi) Creative Commons License identifier identifier identifier

Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, cilt.111, sa.51, ss.18285-18290, 2014 (SCI İndekslerine Giren Dergi) Creative Commons License identifier identifier identifier

Disruption of HDX gene in premature ovarian failure

SYSTEMS BIOLOGY IN REPRODUCTIVE MEDICINE, cilt.59, sa.4, ss.218-222, 2013 (SCI İndekslerine Giren Dergi) Creative Commons License identifier identifier identifier

Two Males with SRY-Positive 46,XX Testicular Disorder of Sex Development

SYSTEMS BIOLOGY IN REPRODUCTIVE MEDICINE, cilt.59, sa.1, ss.42-47, 2013 (SCI İndekslerine Giren Dergi) Creative Commons License identifier identifier identifier

Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, cilt.105, sa.11, ss.4232-4236, 2008 (SCI İndekslerine Giren Dergi) Creative Commons License identifier identifier identifier

MDM2 T309G polymorphism is associated with bladder cancer

ANTICANCER RESEARCH, cilt.26, ss.3473-3475, 2006 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Patients with Essential Tremor Live Longer than their Relatives

21st International Congress of Parkinson's Disease and Movement Disorders, Vancouver, Kanada, 4 - 08 Haziran 2017, cilt.32, sa.754 identifier

Tanı konulmamış hastalarda yeni nesil dizileme ile tanı projeleri

13. ULUSAL SİNİRBİLİM KONGRESİ, Konya, Türkiye, 30 Nisan 2015

DOES TELOMERE SHORTENING IN WOMEN IWTH REHEUMATOID ARTHRITIS PREDICT X CHROMOSOME INACTIVATION BIAS?

33rd European Workshop for Rheumatology Research (EWRR), Prague, Çek Cumhuriyeti, 28 Şubat - 02 Mart 2013, cilt.72 Creative Commons License identifier

Identification of a novel missense mutation in RAD51 in a large family with congenital mirror movements

62nd Annual Meeting of the American Society of Human Genetics, ASHG 2012, San-Francisco, Kostarika, 06 Kasım 2012

SKEWED X CHROMOSOME INACTIVATION IN RHEUMATOID ARTHRITIS WOMEN

31st European Workshop for Rheumatology Research, Amsterdam, Hollanda, 3 - 06 Mart 2011, cilt.70 Creative Commons License identifier

MDM2 T309G polymorphism is associated with bladder cancer

31st Congress of the Federation-of-European-Biochemical-Societies (FEBS), İstanbul, Türkiye, 24 - 29 Haziran 2006, cilt.273, ss.225-226 identifier

MDM2 T309G polymorphism is associated with bladder cancer

EUROPEAN HUMAN GENETICS CONFERENCE 2006, Amsterdam, Hollanda, 06 Mayıs 2006, cilt.14, ss.207

Fransız skleroderma hastalarında X-inaktivasyonu bozukluğu

VIII.Ulusal Tıbbi Genetik Kongresi, Çanakkale, Türkiye, 06 Mayıs 2006