| Incidence and origin of" null" alleles in the (AC) n microsatellite markers DF Callen, AD Thompson, Y Shen, HA Phillips, RI Richards, JC Mulley, ... American journal of human genetics 52 (5), 922, 1993 | 1010 | 1993 |
| A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis M Town, G Jean, S Cherqui, M Attard, L Forestier, SA Whitmore, ... Nature genetics 18 (4), 319-324, 1998 | 751 | 1998 |
| Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance MA Tischfield, HN Baris, C Wu, G Rudolph, L Van Maldergem, W He, ... Cell 140 (1), 74-87, 2010 | 715 | 2010 |
| Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA JR Lo Ten Foe, MA Rooimans, L Bosnoyan-Collins, N Alon, M Wijker, ... Nature genetics 14 (3), 320-323, 1996 | 524 | 1996 |
| Derepression of an endogenous long terminal repeat activates the CSF1R proto-oncogene in human lymphoma B Lamprecht, K Walter, S Kreher, R Kumar, M Hummel, D Lenze, ... Nature medicine 16 (5), 571-579, 2010 | 441 | 2010 |
| Integration of cytogenetic landmarks into the draft sequence of the human genome T BAC Resource Consortium, VG Cheung, N Nowak, W Jang, IR Kirsch, ... Nature 409 (6822), 953-958, 2001 | 392 | 2001 |
| The oncogenic role of miR-155 in breast cancer S Mattiske, RJ Suetani, PM Neilsen, DF Callen Cancer epidemiology, biomarkers & prevention 21 (8), 1236-1243, 2012 | 383 | 2012 |
| Diagnostic yield of genetic testing in epileptic encephalopathy in childhood S Mercimek‐Mahmutoglu, J Patel, D Cordeiro, S Hewson, D Callen, ... Epilepsia 56 (5), 707-716, 2015 | 288 | 2015 |
| The NF1 gene revisited–from bench to bedside YS Yap, JR McPherson, CK Ong, SG Rozen, BT Teh, ASG Lee, DF Callen Oncotarget 5 (15), 5873, 2014 | 274 | 2014 |
| Localization of the human multiple drug resistance gene, MDR1, to 7q21.1 DF Callen, E Baker, RN Simmers, R Seshadri, IB Roninson Human genetics 77 (2), 142-144, 1987 | 272 | 1987 |
| A third Wilms' tumor locus on chromosome 16q MA Maw, PE Grundy, LJ Millow, MR Eccles, RS Dunn, PJ Smith, ... Cancer research 52 (11), 3094-3098, 1992 | 255 | 1992 |
| The sequence and analysis of duplication-rich human chromosome 16 J Martin, C Han, LA Gordon, A Terry, S Prabhakar, X She, G Xie, ... Nature 432 (7020), 988-994, 2004 | 211 | 2004 |
| Mutant p53 drives invasion in breast tumors through up-regulation of miR-155 PM Neilsen, JE Noll, S Mattiske, CP Bracken, PA Gregory, RB Schulz, ... Oncogene 32 (24), 2992-3000, 2013 | 201 | 2013 |
| Mutations in KCNT1 cause a spectrum of focal epilepsies RS Møller, SE Heron, LHG Larsen, CX Lim, MG Ricos, MA Bayly, ... Epilepsia 56 (9), e114-e120, 2015 | 188 | 2015 |
| Ankrd11 is a chromatin regulator involved in autism that is essential for neural development D Gallagher, A Voronova, MA Zander, GI Cancino, A Bramall, MP Krause, ... Developmental cell 32 (1), 31-42, 2015 | 187 | 2015 |
| The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene K Bhalla, HA Phillips, J Crawford, OLD McKenzie, JC Mulley, H Eyre, ... Journal of human genetics 49 (6), 308-311, 2004 | 186 | 2004 |
| Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis JK Nancarrow, E Kremer, K Holman, H Eyre, NA Doggett, D Le Paslier, ... Science 264 (5167), 1938-1941, 1994 | 186 | 1994 |
| Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22. 1 CA Klanke, YR Su, DF Callen, Z Wang, P Meneton, N Baird, ... Genomics 25 (3), 615-622, 1995 | 184 | 1995 |
| Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies E Baker, L Hinton, DF Callen, M Altree, A Dobbie, HJ Eyre, GR Sutherland, ... American journal of medical genetics 107 (4), 285-293, 2002 | 175 | 2002 |
| Structure and chromosomal localization of the human renal kallikrein gene BA Evans, ZX Yun, JA Close, GW Tregear, N Kitamura, S Nakanishi, ... Biochemistry 27 (9), 3124-3129, 1988 | 171 | 1988 |
