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Hans Gille
Hans Gille
clinical laboratory geneticist, AmsterdamUMC
在 amsterdamumc.nl 的电子邮件经过验证
标题
引用次数
引用次数
年份
Frequency and spectrum of cancers in the Peutz-Jeghers syndrome
N Hearle, V Schumacher, FH Menko, S Olschwang, LA Boardman, ...
Clinical Cancer Research 12 (10), 3209-3215, 2006
10702006
Dysplastic changes in prophylactically removed Fallopian tubes of women predisposed to developing ovarian cancer
JMJ Piek, PJ Van Diest, RP Zweemer, JW Jansen, RJJ Poort‐Keesom, ...
The Journal of Pathology: A Journal of the Pathological Society of Great …, 2001
10072001
The Cowden syndrome: a clinical and genetic study in 21 patients
TM Starink, JPW Veen, F Arwert, LP Waal, GG Lange, JJP Gille, ...
Clinical genetics 29 (3), 222-233, 1986
6621986
Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer
TR Rebbeck, N Mitra, F Wan, OM Sinilnikova, S Healey, L McGuffog, ...
Jama 313 (13), 1347-1361, 2015
5752015
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
5201996
Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method
FBL Hogervorst, PM Nederlof, JJP Gille, CJ McElgunn, M Grippeling, ...
Cancer research 63 (7), 1449-1453, 2003
4172003
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study
MJE Kempers, RP Kuiper, CW Ockeloen, PO Chappuis, P Hutter, ...
The lancet oncology 12 (1), 49-55, 2011
3512011
Relative frequency and morphology of cancers in STK11 mutation carriers
W Lim, S Olschwang, JJ Keller, AM Westerman, FH Menko, LA Boardman, ...
Gastroenterology 126 (7), 1788-1794, 2004
3352004
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk
FJ Couch, X Wang, L McGuffog, A Lee, C Olswold, KB Kuchenbaecker, ...
PLoS genetics 9 (3), e1003212, 2013
3332013
Evidence for at least eight Fanconi anemia genes
H Joenje, AB Oostra, M Wijker, FM di Summa, CGM van Berkel, ...
The American Journal of Human Genetics 61 (4), 940-944, 1997
3211997
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
KB Kuchenbaecker, SJ Ramus, J Tyrer, A Lee, HC Shen, J Beesley, ...
Nature genetics 47 (2), 164-171, 2015
3142015
Cell culture models for oxidative stress: superoxide and hydrogen peroxide versus normobaric hyperoxia
JJP Gille, H Joenje
Mutation Research/DNAging 275 (3-6), 405-414, 1992
2591992
Molecular evidence linking primary cancer of the fallopian tube to BRCA1 germline mutations
RP Zweemer, PJ Van Diest, RHM Verheijen, A Ryan, JJP Gille, ...
Gynecologic oncology 76 (1), 45-50, 2000
2292000
A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families
T Peelen, M Van Vliet, A Petrij-Bosch, R Mieremet, C Szabo, ...
American journal of human genetics 60 (5), 1041, 1997
2171997
TBX4 mutations (small patella syndrome) are associated with childhood-onset pulmonary arterial hypertension
WS Kerstjens-Frederikse, EMHF Bongers, MTR Roofthooft, EM Leter, ...
Journal of medical genetics 50 (8), 500-506, 2013
2072013
Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach
JJP Gille, FBL Hogervorst, G Pals, JT Wijnen, RJ Van Schooten, ...
British Journal of Cancer 87 (8), 892-897, 2002
1952002
Recurrence and variability of germline EPCAM deletions in Lynch syndrome
RP Kuiper, LELM Vissers, R Venkatachalam, D Bodmer, E Hoenselaar, ...
Human mutation 32 (4), 407-414, 2011
1892011
Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype
H Joenje, JR Lo Ten Foe, AB Oostra, CG Van Berkel, MA Rooimans, ...
1881995
Renal cancer and pneumothorax risk in Birt–Hogg–Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families
AC Houweling, LM Gijezen, MA Jonker, MBA van Doorn, RA Oldenburg, ...
British journal of cancer 105 (12), 1912-1919, 2011
1792011
Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations
M Castella, R Pujol, E Callén, JP Trujillo, JA Casado, H Gille, FP Lach, ...
Blood, The Journal of the American Society of Hematology 117 (14), 3759-3769, 2011
1602011
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