Jane S Green
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Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
FS Leach, NC Nicolaides, N Papadopoulos, B Liu, J Jen, R Parsons, ...
Cell 75 (6), 1215-1225, 1993
Genetic mapping of a locus predisposing to human colorectal cancer
P Peltomaki, LA Aaltonen, P Sistonen, L Pylkkanen, JP Mecklin, ...
Science 260 (5109), 810-812, 1993
Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene
JB Li, JM Gerdes, CJ Haycraft, Y Fan, TM Teslovich, H May-Simera, H Li, ...
Cell 117 (4), 541-552, 2004
Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients
LA Aaltonen, P Peltomäki, JP Mecklin, H Järvinen, JR Jass, JS Green, ...
Cancer research 54 (7), 1645-1648, 1994
Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24
BW Zanke, CMT Greenwood, J Rangrej, R Kustra, A Tenesa, ...
Nature genetics 39 (8), 989-994, 2007
Von Hippel–Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma
BR Seizinger, GA Rouleau, LJ Ozelius, AH Lane, GE Farmer, JM Lamiell, ...
Nature 332 (6161), 268-269, 1988
The cardinal manifestations of Bardet–Biedl syndrome, a form of Laurence–Moon–Biedl syndrome
JS Green, PS Parfrey, JD Harnett, NR Farid, BC Cramer, G Johnson, ...
New England Journal of Medicine 321 (15), 1002-1009, 1989
Germline mutations in the von Hippel–Lindau disease tumor suppressor gene: correlations with phenotype
F Chen, T Kishida, M Yao, T Hustad, D Glavac, M Dean, JR Gnarra, ...
Human mutation 5 (1), 66-75, 1995
The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations
L Senter, M Clendenning, K Sotamaa, H Hampel, J Green, JD Potter, ...
Gastroenterology 135 (2), 419-428. e1, 2008
Germline Mutations of the MEN1 Gene in Familial Multiple Endocrine Neoplasia Type 1 and Related States
SK Agarwal, M Beth Kester, LV Debelenko, C Heppner, MR Emmert-Buck, ...
Human molecular genetics 6 (7), 1169-1175, 1997
hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds
B Liu, RE Parsons, SR Hamilton, GM Petersen, HT Lynch, P Watson, ...
Cancer Research 54 (17), 4590-4594, 1994
Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer
P Kaurah, A MacMillan, N Boyd, J Senz, A De Luca, N Chun, G Suriano, ...
Jama 297 (21), 2360-2372, 2007
Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome
N Katsanis, PL Beales, MO Woods, RA Lewis, JS Green, PS Parfrey, ...
Nature genetics 26 (1), 67-70, 2000
Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome
Y Fan, MA Esmail, SJ Ansley, OE Blacque, K Boroevich, AJ Ross, ...
Nature genetics 36 (9), 989-993, 2004
Mutations in MKKS cause Bardet-Biedl syndrome
AM Slavotinek, EM Stone, K Mykytyn, JR Heckenlively, JS Green, E Heon, ...
Nature genetics 26 (1), 15-16, 2000
Clinical and genetic epidemiology of Bardet–Biedl syndrome in Newfoundland: A 22‐year prospective, population‐based, cohort study
SJ Moore, JS Green, Y Fan, AK Bhogal, E Dicks, BA Fernandez, ...
American journal of medical genetics Part A 132 (4), 352-360, 2005
Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations.
ER Maher, AR Webster, FM Richards, JS Green, PA Crossey, SJ Payne, ...
Journal of Medical Genetics 33 (4), 328-332, 1996
Germ-line mutations in the von Hippel–Lindau tumor-suppressor gene are similar to somatic von Hippel–Lindau aberrations in sporadic renal cell carcinoma
JM Whaley, J Naglich, L Gelbert, YE Hsia, JM Lamiell, JS Green, ...
American journal of human genetics 55 (6), 1092, 1994
Accumulated clonal genetic alterations in familial and sporadic colorectal carcinomas with widespread instability in microsatellite sequences
T Fujiwara, JM Stolker, T Watanabe, A Rashid, P Longo, JR Eshleman, ...
The American journal of pathology 153 (4), 1063-1078, 1998
The spectrum of renal disease in Laurence–Moon–Biedl syndrome
JD Harnett, JS Green, BC Cramer, G Johnson, L Chafe, P McManamon, ...
New England Journal of Medicine 319 (10), 615-618, 1988
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