| Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1 YJ Crow, DS Chase, J Lowenstein Schmidt, M Szynkiewicz, GMA Forte, ... American journal of medical genetics Part A 167 (2), 296-312, 2015 | 561 | 2015 |
| Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders G Novarino, AG Fenstermaker, MS Zaki, M Hofree, JL Silhavy, ... science 343 (6170), 506-511, 2014 | 560 | 2014 |
| Çocuk istismarı B Kara, Ü Biçer, AS Gökalp Çocuk Sağlığı ve Hastalıkları Dergisi 47 (2), 140-51, 2004 | 560 | 2004 |
| Subclinical vitamin D deficiency is increased in adolescent girls who wear concealing clothing S Hatun, Ö Islam, F Cizmecioglu, B Kara, K Babaoglu, F Berk, AS Gökalp The Journal of nutrition 135 (2), 218-222, 2005 | 282 | 2005 |
| Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ... The American Journal of Human Genetics 105 (2), 267-282, 2019 | 230 | 2019 |
| Kocaeli ilindeki lise öğrencilerinde sağlık açısından riskli davranışların değerlendirilmesi B Kara, Ş Hatun, M Aydoğan, K Babaoğlu, AS Gökalp Çocuk Sağlığı ve Hastalıkları Dergisi 46 (1), 30-7, 2003 | 120 | 2003 |
| Doğum sonrası depresyon B Kara, P Çakmaklı, E Nacak, F Türeci Sted 10 (9), 333-4, 2001 | 79 | 2001 |
| Using the Modified Checklist for Autism in Toddlers in a well-child clinic in Turkey: Adapting the screening method based on culture and setting B Kara, NM Mukaddes, I Altınkaya, D Güntepe, G Gökçay, M Özmen Autism 18 (3), 331-338, 2014 | 71 | 2014 |
| Annelerin emzirme ve süt çocuğu beslenmesi konusundaki bilgi, inanış ve uygulamaları: niteliksel bir araştırma G Samlı, B Kara, PC Ünalan, B Samlı, N Sarper, AS Gökalp Marmara Med J 19 (1), 13-20, 2006 | 71 | 2006 |
| A frameshift mutation of ERLIN2 in recessive intellectual disability, motor dysfunction and multiple joint contractures Y Yıldırım, E Kocasoy Orhan, SA Ugur Iseri, P Serdaroglu-Oflazer, B Kara, ... Human molecular genetics 20 (10), 1886-1892, 2011 | 67 | 2011 |
| Biallelic variants in OTUD6B cause an intellectual disability syndrome associated with seizures and dysmorphic features T Santiago-Sim, LC Burrage, F Ebstein, MJ Tokita, M Miller, W Bi, ... The American Journal of Human Genetics 100 (4), 676-688, 2017 | 65 | 2017 |
| The prevalence of anemia in adolescents: a study from Turkey B Kara, S Çal, A Aydogan, N Sarper Journal of pediatric hematology/oncology 28 (5), 316-321, 2006 | 59 | 2006 |
| Body mass index and complications following major gastrointestinal surgery: a prospective, international cohort study and meta‐analysis EuroSurg Collaborative, R Blanco‐Colino, S Lee, SK Kamarajah, P Vasko, ... Colorectal Disease 20 (8), O215-O225, 2018 | 56 | 2018 |
| New hyperekplexia mutations provide insight into glycine receptor assembly, trafficking, and activation mechanisms A Bode, SE Wood, JGL Mullins, A Keramidas, TD Cushion, RH Thomas, ... Journal of Biological Chemistry 288 (47), 33745-33759, 2013 | 47 | 2013 |
| Adult phenotype and further phenotypic variability in SRD5A3-CDG B Kara, Ö Ayhan, G Gökçay, N Başboğaoğlu, A Tolun BMC medical genetics 15, 1-6, 2014 | 39 | 2014 |
| Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals JE Motelow, G Povysil, RS Dhindsa, KE Stanley, AS Allen, YCA Feng, ... The American Journal of Human Genetics 108 (6), 965-982, 2021 | 37 | 2021 |
| Congenital myasthenic syndromes in Turkey: clinical clues and prognosis with long term follow-up H Durmus, XM Shen, P Serdaroglu-Oflazer, B Kara, Y Parman-Gulsen, ... Neuromuscular Disorders 28 (4), 315-322, 2018 | 34 | 2018 |
| Is there a role for the family and close community to help reduce the risk of postpartum depression in new mothers? A cross-sectional study of Turkish women B Kara, P Ünalan, S Cifçili, DS Cebeci, N Sarper Maternal and Child Health Journal 12, 155-161, 2008 | 31 | 2008 |
| Monogenic lupus due to spondyloenchondrodysplasia with spastic paraparesis and intracranial calcification: case-based review B Kara, Z Ekinci, S Sahin, M Gungor, AS Gunes, K Ozturk, A Adrovic, ... Rheumatology International 40 (11), 1903-1910, 2020 | 29 | 2020 |
| Severe neurodegenerative disease in brothers with homozygous mutation in POLR1A B Kara, Ç Köroğlu, K Peltonen, RC Steinberg, H Maraş Genç, ... European Journal of Human Genetics 25 (3), 315-323, 2017 | 29 | 2017 |
