Identification of the von Hippel-Lindau disease tumor suppressor gene F Latif, K Tory, J Gnarra, M Yao, FM Duh, ML Orcutt, T Stackhouse, ... Science 260 (5112), 1317-1320, 1993 | 3577 | 1993 |
Multicolor spectral karyotyping of human chromosomes E Schröck, S Du Manoir, T Veldman, B Schoell, J Wienberg, ... Science 273 (5274), 494-497, 1996 | 2239 | 1996 |
Clinical features and natural history of von Hippel-Lindau disease ER Maher, JRW Yates, R Harries, C Benjamin, R Harris, AT Moore, ... QJM: An International Journal of Medicine 77 (2), 1151-1163, 1990 | 1166 | 1990 |
Translocation of c-abl oncogene correlates with the presence of a Philadelphia chromosome in chronic myelocytic leukaemia CR Bartram, A de Klein, A Hagemeijer, T van Agthoven, AG van Kessel, ... Nature 306 (5940), 277-280, 1983 | 944 | 1983 |
Genome analysis of the platypus reveals unique signatures of evolution Nature 453 (7192), 175-183, 2008 | 781 | 2008 |
Von Hippel-Lindau disease: a genetic study. ER Maher, L Iselius, JR Yates, M Littler, C Benjamin, R Harris, J Sampson, ... Journal of medical genetics 28 (7), 443-447, 1991 | 736 | 1991 |
Cytogenetic analysis by chromosome painting using DOP‐PCR amplified flow‐sorted chromosomes HÅK Telenius, BAJ Ponder, A Tunnacliffe, AH Pelmear, NP Carter, ... Genes, Chromosomes and Cancer 4 (3), 257-263, 1992 | 716 | 1992 |
Karyotype-phenotype correlations in gonadal dysgenesis and their bearing on the pathogenesis of malformations MA Ferguson-Smith Journal of Medical Genetics 2 (2), 142, 1965 | 686 | 1965 |
Germline mutations in the Von Hippel‐Lindau disease (VHL) gene in families from North America, Europe, and Japan B Zbar, T Kishida, F Chen, L Schmidt, ER Maher, FM Richards, ... Human mutation 8 (4), 348-357, 1996 | 630 | 1996 |
Maternal age specific rates for chromosome aberrations and factors influencing them: report of a collaborative european study on 52 965 amniocenteses MA Ferguson‐Smith, JRW Yates Prenatal diagnosis 4 (7), 5-44, 1984 | 536 | 1984 |
Essential medical genetics ES Tobias, M Connor, M Ferguson-Smith John Wiley & Sons, 2011 | 520 | 2011 |
XY chromosomal interchange in the aetiology of true hermaphroditism and of XX Klinefelter's syndrome MA Ferguson-Smith The Lancet 288 (7461), 475-476, 1966 | 463 | 1966 |
Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype. PA Crossey, FM Richards, K Foster, JS Green, A Prowse, F Latif, ... Human Molecular Genetics 3 (8), 1303-1308, 1994 | 438 | 1994 |
Somatic mutations of the von Hippel—Lindau disease tumour suppressor gene in non-familial clear cell renal carcinoma K Foster, A Prowse, A van den Berg, S Fleming, MMF Hulsbeek, ... Human molecular genetics 3 (12), 2169-2173, 1994 | 431 | 1994 |
Microsatellite evolution—evidence for directionality and variation in rate between species DC Rubinsztein, W Amos, J Leggo, S Goodburn, S Jain, SH Li, ... Nature genetics 10 (3), 337-343, 1995 | 399 | 1995 |
A complete comparative chromosome map for the dog, red fox, and human and its integration with canine genetic maps F Yang, PCM O'brien, BS Milne, AS Graphodatsky, N Solanky, V Trifonov, ... Genomics 62 (2), 189-202, 1999 | 398 | 1999 |
Bird-like sex chromosomes of platypus imply recent origin of mammal sex chromosomes F Veyrunes, PD Waters, P Miethke, W Rens, D McMillan, AE Alsop, ... Genome research 18 (6), 965-973, 2008 | 382 | 2008 |
Observations on the satellited human chromosomes MA Ferguson-Smith, SD Handmaker, ABJ Hopkins The Lancet 277 (7178), 638-640, 1961 | 367 | 1961 |
Mammalian karyotype evolution MA Ferguson-Smith, V Trifonov Nature Reviews Genetics 8 (12), 950-962, 2007 | 364 | 2007 |
Multicolour spectral karyotyping of mouse chromosomes M Liyanage, A Coleman, S Manoir, T Veldman, S McCormack, ... Nature genetics 14 (3), 312-315, 1996 | 355 | 1996 |