| Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations MG Butler, MJ Dasouki, XP Zhou, Z Talebizadeh, M Brown, TN Takahashi, ... Journal of medical genetics 42 (4), 318-321, 2005 | 915 | 2005 |
| Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy MG Butler, DC Bittel, N Kibiryeva, Z Talebizadeh, T Thompson Pediatrics 113 (3), 565-573, 2004 | 346 | 2004 |
| Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism Z Talebizadeh, DY Lam, MF Theodoro, DC Bittel, GH Lushington, ... Journal of medical genetics 43 (5), e21-e21, 2006 | 210 | 2006 |
| Feasibility and relevance of examining lymphoblastoid cell lines to study role of microRNAs in autism Z Talebizadeh, MG Butler, MF Theodoro Autism Research 1 (4), 240-250, 2008 | 187 | 2008 |
| Association of the 103I MC4R allele with decreased body mass in 7937 participants of two population based surveys IM Heid, C Vollmert, A Hinney, A Döring, F Geller, H Löwel, HE Wichmann, ... Journal of Medical Genetics 42 (4), e21-e21, 2005 | 148 | 2005 |
| Comparison of X-chromosome inactivation patterns in multiple tissues from human females DC Bittel, MF Theodoro, N Kibiryeva, W Fischer, Z Talebizadeh, MG Butler Journal of medical genetics 45 (5), 309-313, 2008 | 122 | 2008 |
| X chromosome gene expression in human tissues: male and female comparisons Z Talebizadeh, SD Simon, MG Butler Genomics 88 (6), 675-681, 2006 | 121 | 2006 |
| snoTARGET shows that human orphan snoRNA targets locate close to alternative splice junctions PS Bazeley, V Shepelev, Z Talebizadeh, MG Butler, L Fedorova, V Filatov, ... Gene 408 (1-2), 172-179, 2008 | 118 | 2008 |
| Body composition and fatness patterns in Prader‐Willi syndrome: comparison with simple obesity MF Theodoro, Z Talebizadeh, MG Butler Obesity 14 (10), 1685-1690, 2006 | 118 | 2006 |
| Insulin resistance and obesity‐related factors in Prader–Willi syndrome: Comparison with obese subjects Z Talebizadeh, MG Butler Clinical genetics 67 (3), 230-239, 2005 | 116 | 2005 |
| Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD DC Bittel, N Kibiryeva, Z Talebizadeh, MG Butler Journal of Medical Genetics 40 (8), 568-574, 2003 | 100 | 2003 |
| Phenotyping, Etiological Factors, and Biomarkers: Toward Precision Medicine in Autism Spectrum Disorders. B DQ, MAS CONSORTIUM.. J Dev Behav Pediatr, 659-73, 2016 | 84 | 2016 |
| Brief report: non-random X chromosome inactivation in females with autism Z Talebizadeh, DC Bittel, OJ Veatch, N Kibiryeva, MG Butler Journal of autism and developmental disorders 35, 675-681, 2005 | 83 | 2005 |
| Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss Z Talebizadeh, PM Kelley, JW Askew, KW Beisel, SD Smith Human mutation 14 (6), 493-501, 1999 | 81 | 1999 |
| Plasma peptide YY and ghrelin levels in infants and children with Prader-Willi syndrome MG Butler, DC Bittel, Z Talebizadeh Journal of Pediatric Endocrinology and Metabolism 17 (9), 1177-1184, 2004 | 71 | 2004 |
| Autism Genetic Database (AGD): a comprehensive database including autism susceptibility gene-CNVs integrated with known noncoding RNAs and fragile sites G Matuszek, Z Talebizadeh BMC medical genetics 10, 1-7, 2009 | 69 | 2009 |
| Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism? Z Talebizadeh, DC Bittel, OJ Veatch, MG Butler, TN Takahashi, JH Miles, ... Journal of autism and developmental disorders 34, 735-736, 2004 | 58 | 2004 |
| Genetic studies of complex human diseases: characterizing SNP-disease associations using Bayesian networks B Han, X Chen, Z Talebizadeh, H Xu BMC systems biology 6, 1-12, 2012 | 57 | 2012 |
| Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37 KT Booth, JW Askew, Z Talebizadeh, PLM Huygen, J Eudy, J Kenyon, ... Genetics in Medicine 21 (4), 948-954, 2019 | 47 | 2019 |
| No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD) Z Talebizadeh, DC Bittel, JH Miles, N Takahashi, CH Wang, N Kibiryeva, ... Journal of Medical Genetics 39 (11), e70-e70, 2002 | 43 | 2002 |
