Ozgur Cogulu (Özgür Çoğulu, ÖzgÜr Çoğulu)

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 21

Top Topics

Transcription Factor

Intellectual Disability

Acute Lymphoblastic Leukemia

Top Venues

Journal of clinical research in pediatric endocrinology

BioMed research international

European journal of haematology

Turkish journal of medical sciences

This page only lists publications with an associated author ORCID identifier.

Publications

Ferda Evin, Tahir Atik, Hüseyin Onay, Ruhsar Damla Gökşen Şimşek, Şükran Darcan, Ozgur Cogulu, Samim Özen
Effectiveness of whole exome sequencing analyses in the molecular diagnosis of osteogenesis imperfecta. Journal of pediatric endocrinology & metabolism : JPEM (2024)
Cem Karadeniz, Kaan Yıldız, Sedef Öksüz, Rüveyda Nur Keçici, Ozgur Cogulu
A case of Williams syndrome with Wolff-Parkinson-White syndrome. Birth defects research 116 (7) (2024)
Esra Isik, Yesim Aydinok, Canan Albayrak, Basak Durmus, Zeynep Karakas, Mehmet Fatih Orhan, Nazan Sarper, Sultan Aydin Köker, Selma Unal, Yeşim Oymak, Nihal Karadaş, Ayşen Türedi Yıldırım, Davut Albayrak, Funda Tayfun Küpesiz, Deniz Tuğcu, Serap Karaman, Mahmut Töbü, Ekrem Ünal, Alper Ozcan, Sule Unal, Tekin Aksu, Ayşegül Ünüvar, Mustafa Bilici, Fatih Mehmet Azık, Yilmaz Ay, Sema Aylan Gelen, Emine Zengin, Esin Albudak, Ibrahim Eker, Taner Karakaya, Ozgur Cogulu, Ferda Özkınay, Tahir Atik
Identification of the molecular etiology in rare congenital hemolytic anemias using next-generation sequencing with exome-based copy number variant analysis. European journal of haematology (2024)
Esra Isik, Yesim Aydinok, Canan Albayrak, Basak Durmus, Zeynep Karakas, Mehmet Fatih Orhan, Nazan Sarper, Sultan Aydin Köker, Selma Unal, Yeşim Oymak, Nihal Karadaş, Ayşen Türedi Yıldırım, Davut Albayrak, Funda Tayfun Küpesiz, Deniz Tuğcu, Serap Karaman, Mahmut Töbü, Ekrem Ünal, Alper Ozcan, Sule Unal, Tekin Aksu, Ayşegül Ünüvar, Mustafa Bilici, Fatih Mehmet Azık, Yilmaz Ay, Sema Aylan Gelen, Emine Zengin, Esin Albudak, Ibrahim Eker, Taner Karakaya, Ozgur Cogulu, Ferda Özkınay, Tahir Atik
Identification of the molecular etiology in rare congenital hemolytic anemias using next-generation sequencing with exome-based copy number variant analysis. European journal of haematology 113 (1) (2024)
Ferda Evin, Tahir Atik, Hüseyin Onay, Ruhsar Damla Gökşen Şimşek, Şükran Darcan, Ozgur Cogulu, Samim Özen
Effectiveness of whole exome sequencing analyses in the molecular diagnosis of osteogenesis imperfecta. Journal of pediatric endocrinology & metabolism : JPEM 37 (8) (2024)
Mehmet Burak Durmaz, Hilmi Bolat, Zehra Cengisiz, Fuat Akercan, Tuba Sözen Türk, Erhan Parıltay, Aslı Ece Solmaz, Mert Kazandi, Emin Karaca, Asude Alpman Durmaz, Ayça Aykut, Sermet Sağol, Haluk Akın, Ferda Özkınay, Ozgur Cogulu
20-year experience on prenatal diagnosis in a reference university medical genetics center in Turkey Turkish journal of medical sciences 51 (4) (2021)
Mehmet Burak Durmaz, Bakiye Goker Bagca, Ozgur Cogulu, Sunde Yilmaz Susluer, Araz Alpay, Serap Aksoylar, Cumhur Gunduz
Antileukemic Effects of Anti-miR-146a, Anti-miR-155, Anti-miR-181a, and Prednisolone on Childhood Acute Lymphoblastic Leukemia. BioMed research international 2021 (2021)
Necil Kütükçüler, Ezgi Topyildiz, Afig Berdeli, Burcu Guven, Ayça Aykut, Asude Alpman Durmaz, Ozgur Cogulu, Guzide Aksu, Neslihan Edeer Karaca
Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA-2; PLCG2): Striking clinical phenotypic overlap and difference. Clinical case reports 9 (4) (2021)
Birsen Şentürk Pilan, Nazlı Burcu Özbaran, Didem Çelik, Tuğçe Özcan, Samim Özen, Ruhsar Damla Gökşen Şimşek, İbrahim Ulman, Ali Avanoğlu, Sibel Tiryaki, Hüseyin Onay, Ozgur Cogulu, Ferda Özkınay, Şükran Darcan
Quality of Life and Psychological Well-being in Children and Adolescents with Disorders of Sex Development Journal of clinical research in pediatric endocrinology 13 (1) (2020)
Esra Isik, Duygu Arican, Tahir Atik, Joo Enn Ooi, Şükran Darcan, Samim Özen, Pelin Özlem Şimsek Kiper, Gülen Eda Utine, Ozgur Cogulu, Ferda Özkınay
A rare cause of syndromic short stature: 3M syndrome in three families. American journal of medical genetics. Part A 185 (2) (2020)
Asude Alpman Durmaz, Ayça Aykut, Tahir Atik, Samim Özen, Durdugül Ayyıldız Emecen, Aysun Ata, Esra Isik, Ruhsar Damla Gökşen Şimşek, Ozgur Cogulu, Ferda Özkınay
A New Cause of Obesity Syndrome Associated with a Mutation in the Carboxypeptidase Gene Detected in Three Siblings with Obesity, Intellectual Disability and Hypogonadotropic Hypogonadism Journal of clinical research in pediatric endocrinology 13 (1) (2020)
Semra Gürsoy, Filiz Hazan, Ayça Aykut, Özlem Nalbantoğlu, Hüseyin Anil Korkmaz, Korcan Demir, Behzat Ozkan, Ozgur Cogulu
Detection of SHOX Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature Journal of clinical research in pediatric endocrinology 12 (4) (2020)
Fuat Kızılay, Bora Irer, Deniz Özalp Kızılay, Adnan Şimşir, Serdar Kalemci, Volkan Sen, Baris Altay, Ozgur Cogulu
Evaluation of lower urinary tract symptoms in children with Down syndrome: A prospective, case-controlled cohort study. Neurourology and urodynamics 39 (2) (2020)
Esra Isik, Hüseyin Onay, Tahir Atik, Aslı Ece Solmaz, Samim Özen, Ozgur Cogulu, Şükran Darcan, Ferda Özkınay
A Neurofibromatosis Noonan Syndrome Patient Presenting with Abnormal External Genitalia Journal of clinical research in pediatric endocrinology 12 (1) (2019)
Samim Özen, Tahir Atik, Özlem Korkmaz, Hüseyin Onay, Damla Gökşen, Ferda Özkınay, Ozgur Cogulu, Şükran Darcan
Aromatase Deficiency in Two Siblings with 46,XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in the CYP19A1 Gene Journal of clinical research in pediatric endocrinology 12 (1) (2019)
Mehmet Burak Durmaz, Hasan Taslidere, Guldane Koturoglu, Cumhur Gunduz, Mehmet Orman, Ozgur Cogulu
Determination of Lymphocyte Cytokinesis-Block Micronucleus Values in Apparently Healthy Children by means of Age and Sex. BioMed research international 2019 (2019)
Necil Kütükçüler, Neslihan Edeer Karaca, Guzide Aksu, Ayca Aykut, Erhan Pariltay, Ozgur Cogulu
An X-Linked Hyper-IgM Patient Followed Successfully for 23 Years without Hematopoietic Stem Cell Transplantation. Case reports in immunology 2018 (2018)
Taha Resid Ozdemir, Neslihan Edeer Karaca, Jan Davis Marshall, Necil Kutukculer, Guzide Aksu, Riza Koksal Ozgul, Aysegul Ozanturk, Esra Isik, Bilcag Akgun, Hamiyet Hekimci Ozdemir, Sukran Darcan, Ferda Ozkinay, Ozgur Cogulu
Immunodeficiency in a Child with Alström Syndrome. Indian journal of pediatrics 85 (10) (2018)
Betül Siyah Bilgin, Özgün Uygur, Demet Terek, Ozge Koroglu, Mehmet Yalaz, Mete Akisü, Ozgur Cogulu, Nilgun Kultursay
Reference values of anthropometric measurements in healthy late preterm and term infants Turkish journal of medical sciences 48 (4) (2018)
Ozgur Cogulu, Jacqueline Schoumans, Gokce A Toruner, Urszula Demkow, Emin Karaca, Asude Alpman Durmaz
Laboratory Genetic Testing in Clinical Practice 2016. BioMed research international 2017 (2017)
Biray Erturk, Emin Karaca, Ayça Aykut, Mehmet Burak Durmaz, Ahmet Guler, Baris Buke, Ahmet Ozgur Yeniel, Ahmet Mete Ergenoğlu, Ferda Ozkinay, Mehmet Ozeren, Mert Kazandi, Fuat Akercan, Sermet Sagol, Cumhur Gunduz, Ozgur Cogulu
Prenatal Evaluation of MicroRNA Expressions in Pregnancies with Down Syndrome. BioMed research international 2016 (2016)