The DNA sequence of human chromosome 22 I Dunham, AR Hunt, JE Collins, R Bruskiewich, DM Beare, M Clamp, ... Nature 402 (6761), 489-495, 1999 | 1446 | 1999 |
TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome S Merscher, B Funke, JA Epstein, J Heyer, A Puech, MM Lu, RJ Xavier, ... Cell 104 (4), 619-629, 2001 | 1000 | 2001 |
22q11. 2 deletion syndrome DM McDonald-McGinn, KE Sullivan, B Marino, N Philip, A Swillen, ... Nature reviews Disease primers 1 (1), 1-19, 2015 | 913 | 2015 |
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. M Karayiorgou, MA Morris, B Morrow, RJ Shprintzen, R Goldberg, ... Proceedings of the National Academy of Sciences 92 (17), 7612-7616, 1995 | 738 | 1995 |
Meiotic pachytene arrest in MLH1-deficient mice W Edelmann, PE Cohen, M Kane, K Lau, B Morrow, S Bennett, A Umar, ... Cell 85 (7), 1125-1134, 1996 | 686 | 1996 |
A common molecular basis for rearrangement disorders on chromosome 22q11 L Edelmann, RK Pandita, E Spiteri, B Funke, R Goldberg, N Palanisamy, ... Human molecular genetics 8 (7), 1157-1167, 1999 | 529 | 1999 |
Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives. AE Pulver, G Nestadt, R Goldberg, RJ Shprintzen, M Lamacz, ... Journal of Nervous and Mental Disease, 1994 | 506 | 1994 |
Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients C Carlson, H Sirotkin, R Pandita, R Goldberg, J McKie, R Wadey, ... The American Journal of Human Genetics 61 (3), 620-629, 1997 | 410 | 1997 |
Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome L Edelmann, RK Pandita, BE Morrow The American Journal of Human Genetics 64 (4), 1076-1086, 1999 | 395 | 1999 |
Association of codon 108/158 catechol‐O‐methyltransferase gene polymorphism with the psychiatric manifestations of velo‐cardio‐facial syndrome HM Lachman, B Morrow, R Shprintzen, S Veit, SS Parsia, G Faedda, ... American journal of medical genetics 67 (5), 468-472, 1996 | 390 | 1996 |
VEGF: a modifier of the del22q11 (DiGeorge) syndrome? I Stalmans, D Lambrechts, S Jansen, J Wang, S Maity, P Kneer, ... Nature medicine 9 (2), 173-182, 2003 | 316 | 2003 |
Abraham's children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry G Atzmon, L Hao, I Pe'er, C Velez, A Pearlman, PF Palamara, B Morrow, ... The American Journal of Human Genetics 86 (6), 850-859, 2010 | 281 | 2010 |
Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome B Morrow, R Goldberg, C Carlson, RD Gupta, H Sirotkin, J Collins, ... American journal of human genetics 56 (6), 1391, 1995 | 279 | 1995 |
Microduplication and triplication of 22q11. 2: a highly variable syndrome TM Yobb, MJ Somerville, L Willatt, HV Firth, K Harrison, J MacKenzie, ... The American Journal of Human Genetics 76 (5), 865-876, 2005 | 272 | 2005 |
Genomic disorders on 22q11 HE McDermid, BE Morrow The American Journal of Human Genetics 70 (5), 1077-1088, 2002 | 262 | 2002 |
Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage J Liao, L Kochilas, S Nowotschin, JS Arnold, VS Aggarwal, JA Epstein, ... Human molecular genetics 13 (15), 1577-1585, 2004 | 228 | 2004 |
AT-rich palindromes mediate the constitutional t (11; 22) translocation L Edelmann, E Spiteri, K Koren, V Pulijaal, MG Bialer, A Shanske, ... The American Journal of Human Genetics 68 (1), 1-13, 2001 | 198 | 2001 |
Suppression of neural fate and control of inner ear morphogenesis by Tbx1 S Raft, S Nowotschin, J Liao, BE Morrow Oxford University Press for The Company of Biologists Limited 131 (8), 1801-1812, 2004 | 191 | 2004 |
REB1, a yeast DNA-binding protein with many targets, is essential for growth and bears some resemblance to the oncogene myb QD Ju, BE Morrow, JR Warner Molecular and cellular biology 10 (10), 5226-5234, 1990 | 175 | 1990 |
Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders. C Carlson, D Papolos, RK Pandita, GL Faedda, S Veit, R Goldberg, ... American journal of human genetics 60 (4), 851, 1997 | 156 | 1997 |