Sefer Kumandaş - Publications, H-index & Citations

Sefer Kumandaş

erciyes university

30H指数

220论文数

2.9K被引数

收录论文 12

发表时间

Structural Variant and Repeat Expansion Findings Identified by Optical Genome Mapping in Complex Autism Spectrum Disorder With Concomitant Neurodevelopmental Disorders 光学基因组图谱在伴有神经发育障碍的复杂自闭症谱系障碍中识别的结构变异和重复扩展发现

Human Mutation

IF3.7

2026-06-11

OAAI

Mehmet Burak Mutlu; Özge Beyza Gündoğdu Öğütlü; Özlem Öz; Fahrettin Duymuş; Serhat Seyhan; Ayşe Gül Bayrak Tokaç; Esad Tezcan; Hakan Öğütlü; Fatma Demiryılmaz; Nurcan Silahtarlıoğlu; Kader Bilgil; Sümeyye Elma; Murat Erdoğan; Hakan Gümüş; Sefer Kumandaş; Fethiye Kılıçaslan

Evaluation of immunization status in patients with cerebral palsy: a multicenter CP-VACC study

EUROPEAN JOURNAL OF PEDIATRICS

IF2.6

2021-08-05

OAAI

Bozkaya-Yilmaz, Sema; Karadag-Oncel, Eda; Olgac-Dundar, Nihal; Gencpinar, Pinar; Sarioglu, Berrak; Arican, Pinar; Ersen, Atilla; Yilmaz-Ciftdogan, Dilek; Yuksel, Merve Feyza; Bektas, Omer; Teber, Serap; Kilic, Betul; Calik, Mustafa; Karaca, Meryem; Canpolat, Mehmet; Kumandas, Sefer; Per, Huseyin; Gumus, Hakan; Ozturk, Selcan; Okuyaz, Cetin; Komur, Mustafa; Ipek, Rojan; Ozbudak, Pinar; Arhan, Ebru; Ince, Hulya; Gurbuz, Gurkan; Mert, Gulen Gul; Ozcan, Neslihan; Turker, Akgun Olmez; Gazeteci-Tekin, Hande; Kirik, Serkan; Gunbey, Ceren; Carman, Kursat Bora; Yarar, Coskun; Cavusoglu, Dilek

The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice

MOVEMENT DISORDERS

IF7.6

2021-02-24

PREAI

Vural, Atay; Simsir, Gulsah; Tekgul, Seyma; Kocoglu, Cemile; Akcimen, Fulya; Kartal, Ece; Sen, Nesli E.; Lahut, Suna; Omur, Ozgur; Saner, Nazan; Gul, Tugce; Bayraktar, Elif; Palvadeau, Robin; Tunca, Ceren; Cetinkaya, Caroline Pirkevi; Eken, Asli Gundogdu; Sahbaz, Irmak; Koc, Muge Kovancilar; Cakmak, Ozgur Oztop; Hanagasi, Hasmet; Bilgic, Basar; Eraksoy, Mefkure; Gunduz, Aysegul; Apaydin, Hulya; Kiziltan, Gunes; Ozekmekci, Sibel; Siva, Aksel; Altintas, Ayse; Gulec, Zeynep E. Kaya; Parman, Yesim; Oflazer, Piraye; Deymeer, Feza; Durmus, Hacer; Sahin, Erdi; Cakar, Arman; Tufekcioglu, Zeynep; Tekturk, Pinar; Corbali, M. Osman; Tireli, Hulya; Akdal, Gulden; Yis, Uluc; Hiz, Semra; Sengun, Ihsan; Bora, Elcin; Serdaroglu, Gul; Ozbek, Sevda Erer; Agan, Kadriye; Gunal, Dilek Ince; Us, Onder; Kurt, Semiha G.; Aksoy, Durdane; Tokcaer, Ayse Bora; Elmas, Muhsin; Gultekin, Murat; Kumandas, Sefer; Acer, Hamit; Ozcora, Gul D. Kaya; Yayla, Vildan; Soysal, Aysun; Genc, Gencer; Gulluoglu, Halil; Kotan, Dilcan; Ayas, Zeynep Ozozen; Sahin, Huseyin A.; Tan, Ersin; Topcu, Meral; Topcuoglu, Esen Saka; Akbostanci, Cenk; Koc, Filiz; Ertan, Sibel; Elibol, Bulent; Basak, A. Nazli

Loss of Protocadherin-12 Leads to Diencephalic-Mesencephalic Junction Dysplasia Syndrome

ANNALS OF NEUROLOGY

IF7.7

2018-10-04

OAAI

Guemez-Gamboa, Alicia; Caglayan, Ahmet Okay; Stanley, Valentina; Gregor, Anne; Zaki, Maha S.; Saleem, Sahar N.; Musaev, Damir; McEvoy-Venneri, Jennifer; Belandres, Denice; Akizu, Naiara; Silhavy, Jennifer L.; Schroth, Jana; Rosti, Rasim Ozgur; Copeland, Brett; Lewis, Steven M.; Fang, Rebecca; Issa, Mahmoud Y.; Per, Huseyin; Gumus, Hakan; Bayram, Ayse Kacar; Kumandas, Sefer; Akgumus, Gozde Tugce; Erson-Omay, Emine Z.; Yasuno, Katsuhito; Bilguvar, Kaya; Heimer, Gali; Pillar, Nir; Shomron, Noam; Weissglas-Volkov, Daphna; Porat, Yuval; Einhorn, Yaron; Gabriel, Stacey; Ben-Zeev, Bruria; Gunel, Murat; Gleeson, Joseph G.

Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors (vol 84, pg 1226, 2014)

NEURON

IF15

2015-01-01

OAAI

Mishra-Gorur, Ketu; Caglayan, Ahmet Okay; Schaffer, Ashleigh E.; Chabu, Chiswili; Henegariu, Octavian; Vonhoff, Fernando; Akgumus, Gozde Tugce; Nishimura, Sayoko; Han, Wenqi; Tu, Shu; Baran, Burcin; Gumus, Hakan; Dilber, Cengiz; Zaki, Maha S.; Hossni, Heba A. A.; Riviere, Jean-Baptiste; Kayserili, Hulya; Spencer, Emily G.; Rosti, Rasim O.; Schroth, Jana; Per, Huseyin; Caglar, Caner; Caglar, Cagri; Dolen, Duygu; Baranoski, Jacob F.; Kumandas, Sefer; Minja, Frank J.; Erson-Omay, E. Zeynep; Mane, Shrikant M.; Lifton, Richard P.; Xu, Tian; Keshishian, Haig; Dobyns, William B.; Chi, Neil C.; Sestan, Nenad; Louvi, Angeliki; Bilguvar, Kaya; Yasuno, Katsuhito; Gleeson, Joseph G.; Gunel, Murat

Childhood Stroke: Results of 130 Children From a Reference Center in Central Anatolia, Turkey

PEDIATRIC NEUROLOGY

IF2.1

2014-06-01

PREAI

Per, Huseyin; Unal, Ekrem; Poyrazoglu, Hatice Gamze; Ozdemir, Mehmet Akif; Donmez, Halil; Gumus, Hakan; Uzum, Kazim; Canpolat, Mehmet; Akyildiz, Basak Nur; Coskun, Abdulhakim; Kurtsoy, Ali; Kumandas, Sefer

THE FIRST TURKISH CASE OF GLUCOSE TRANSPORTER TYPE 1 DEFICIENCY SYNDROME (GLUT 1D) WITH MOLECULAR STUDIES

PEDIATRIC RESEARCH

IF3.1

2010-11-01

OAAI

Gumus, H.; Caglayan, A. O.; Per, H.; Kumandas, S.; Engelstad, K.; Kardes, F.; De Vivo, D.

INTRACRANIAL HEMORRHAGES AND LATE HEMORRHAGIC DISEASE ASSOCIATED CHOLESTATIC LIVER DISEASE

PEDIATRIC RESEARCH

IF3.1

2010-11-01

OAAI

Per, H.; Arslan, D.; Gumus, H.; Coskun, A.; Kumandas, S.

Maternal uniparental isodisomy is responsible for serious molybdenum cofactor deficiency

DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

IF4.3

2010-08-16

OAAI

Gumus, Hakan; Ghesquiere, Stijn; Per, Hueseyin; Kondolot, Meda; Ichida, Kimiyoshi; Poyrazoglu, Gamze; Kumandas, Sefer; Engelen, John; Dundar, Munis; Caglayan, Ahmet Okay

Levetiracetam monotherapy in newly diagnosed cryptogenic west syndrome

PEDIATRIC NEUROLOGY

IF2.1

2007-11-01

PREAI

Guemues, Hakan; Kumandas, Sefer; Per, Huseyin

Molybdenum cofactor deficiency:: Clinical features in a Turkish patient

BRAIN & DEVELOPMENT

IF1.3

2007-07-01

PREAI

Per, Huseyin; Gumus, Hakan; Ichida, Kimiyoshi; Caglayan, Okay; Kumandas, Sefer