ติดตาม
R Ramesar
R Ramesar
Professor of Human Genetics, University of Cape Town, South Africa
ยืนยันอีเมลแล้วที่ uct.ac.za
ชื่อ
อ้างโดย
อ้างโดย
ปี
LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development
Y Gong, RB Slee, N Fukai, G Rawadi, S Roman-Roman, AM Reginato, ...
Cell 107 (4), 513-523, 2001
27172001
Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial
J Burn, AM Gerdes, F Macrae, JP Mecklin, G Moeslein, S Olschwang, ...
The Lancet 378 (9809), 2081-2087, 2011
11802011
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database
BA Thompson, AB Spurdle, JP Plazzer, MS Greenblatt, K Akagi, ...
Nature genetics 46 (2), 107-115, 2014
5222014
Reconstructing prehistoric African population structure
P Skoglund, JC Thompson, ME Prendergast, A Mittnik, K Sirak, ...
Cell 171 (1), 59-71. e21, 2017
4272017
The molecular genetics of cognition: dopamine, COMT and BDNF
J Savitz, M Solms, R Ramesar
Genes, brain and behavior 5 (4), 311-328, 2006
4012006
Effect of aspirin or resistant starch on colorectal neoplasia in the Lynch syndrome
J Burn, DT Bishop, JP Mecklin, F Macrae, G Möslein, S Olschwang, ...
New England Journal of Medicine 359 (24), 2567-2578, 2008
3762008
Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind …
J Burn, H Sheth, F Elliott, L Reed, F Macrae, JP Mecklin, G Möslein, ...
The Lancet 395 (10240), 1855-1863, 2020
3622020
Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13)
AB McKie, JC McHale, TJ Keen, EE Tarttelin, R Goliath, ...
Human molecular genetics 10 (15), 1555-1562, 2001
3492001
Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13
Y Gong, M Vikkula, L Boon, J Liu, P Beighton, R Ramesar, L Peltonen, ...
American journal of human genetics 59 (1), 146, 1996
3321996
Waardenberg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: First report of the WS consortium
LA Farrer, KM Grundfast, J Amos, KS Arnos, JH Asher, P Beighton, ...
American journal of human genetics 50 (5), 902, 1992
2971992
Neuropsychological dysfunction in bipolar affective disorder: a critical opinion
J Savitz, M Solms, R Ramesar
Bipolar disorders 7 (3), 216-235, 2005
2772005
Exploring researchers’ experiences of working with a researcher-driven, population-specific community advisory board in a South African schizophrenia genomics study
MM Campbell, E Susser, J de Vries, A Baldinger, G Sibeko, MM Mndini, ...
BMC Medical Ethics 16, 1-9, 2015
2602015
CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness
LM Astuto, JM Bork, MD Weston, JW Askew, RR Fields, DJ Orten, ...
The American Journal of Human Genetics 71 (2), 262-275, 2002
2582002
Enabling the genomic revolution in Africa: H3Africa is developing capacity for health-related genomics research in Africa
H3Africa Consortium
Science (New York, NY) 344 (6190), 1346, 2014
2342014
Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onset
LPW Ranum, MY Chung, S Banfi, A Bryer, LJ Schut, R Ramesar, ...
American journal of human genetics 55 (2), 244, 1994
2271994
Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa
MD Weston, JD Eudy, S Fujita, SF Yao, S Usami, C Cremers, J Greenburg, ...
The American Journal of Human Genetics 66 (4), 1199-1210, 2000
2222000
Warriors versus worriers: the role of COMT gene variants
DJ Stein, TK Newman, J Savitz, R Ramesar
CNS spectrums 11 (10), 745-748, 2006
2172006
Autosomal dominant craniometaphyseal dysplasia is caused by mutations in the transmembrane protein ANK
E Reichenberger, V Tiziani, S Watanabe, L Park, Y Ueki, C Santanna, ...
The American Journal of Human Genetics 68 (6), 1321-1326, 2001
2162001
A mutation in the variable repeat region of the aggrecan gene (AGC1) causes a form of spondyloepiphyseal dysplasia associated with severe, premature osteoarthritis
L Gleghorn, R Ramesar, P Beighton, G Wallis
The American Journal of Human Genetics 77 (3), 484-490, 2005
2012005
Genetic variants implicated in personality: a review of the more promising candidates
JB Savitz, RS Ramesar
American journal of medical genetics Part B: Neuropsychiatric genetics 131 …, 2004
1932004
ระบบไม่สามารถดำเนินการได้ในขณะนี้ โปรดลองใหม่อีกครั้งในภายหลัง
บทความ 1–20