about
X-linked late-onset sensorineural deafness caused by a deletion involving OA1 and a novel gene containing WD-40 repeatsThe clinical phenotype of Lynch syndrome due to germ-line PMS2 mutationsPALB2: research reaching to clinical outcomes for women with breast cancerPALB2, CHEK2 and ATM rare variants and cancer risk: data from COGSPractical guidelines addressing ethical issues pertaining to the curation of human locus-specific variation databases (LSDBs)Risks of Lynch syndrome cancers for MSH6 mutation carriers.Body mass index in early adulthood and colorectal cancer risk for carriers and non-carriers of germline mutations in DNA mismatch repair genesMetachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgeryFamily history of colorectal cancer in BRAF p.V600E-mutated colorectal cancer cases.Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia.Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families.An investigation into FOXE1 polyalanine tract length in premature ovarian failure.A PALB2 mutation associated with high risk of breast cancer.Morphological predictors of BRCA1 germline mutations in young women with breast cancer.Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype.Body mass index in early adulthood and endometrial cancer risk for mismatch repair gene mutation carriers.Red cells from ferrochelatase-deficient erythropoietic protoporphyria patients are resistant to growth of malarial parasites.How to catch all those mutations--the report of the third Human Variome Project Meeting, UNESCO Paris, May 2010.High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registryImproving family communication after a new genetic diagnosis: a randomised controlled trial of a genetic counselling intervention.Fertility and apparent genetic anticipation in Lynch syndrome.DNA microsatellite instability and mismatch repair protein loss in adenomas presenting in hereditary non-polyposis colorectal cancer.Mal de Meleda in Indonesia: Mutations in the SLURP1 gene appear to be ubiquitous.Screening practices of unaffected people at familial risk of colorectal cancer.Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study.Mutation screening of PALB2 in clinically ascertained families from the Breast Cancer Family Registry.Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22.Lynch syndrome and cervical cancerRisk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene.Aspirin, Ibuprofen, and the Risk of Colorectal Cancer in Lynch Syndrome.Female Hormonal Factors and the Risk of Endometrial Cancer in Lynch Syndrome.Screening practices of Australian men and women categorized as "at or slightly above average risk" of colorectal cancer.Risks of primary extracolonic cancers following colorectal cancer in lynch syndromeOutcomes of a randomised controlled trial of a complex genetic counselling intervention to improve family communicationGermline mutations in PMS2 and MLH1 in individuals with solitary loss of PMS2 expression in colorectal carcinomas from the Colon Cancer Family Registry Cohort.Fertility after young-onset colorectal cancer: a study of subjects with Lynch syndrome.Risks of colorectal and other cancers after endometrial cancer for women with Lynch syndromeAre the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers?Prevalence of PALB2 mutations in Australasian multiple-case breast cancer familiesTumour morphology predicts PALB2 germline mutation status.
P50
Q22010051-81AE0AA6-49AA-450A-AA2F-01C51766A98FQ24655454-45E6C2E9-04CF-496A-B5D2-C98AB43A2D1FQ26751309-29F8F7BA-7525-4F78-8EDE-8A199132A60CQ28584533-F1FCE88F-58B7-4225-B908-5AA56EB02EA2Q28744635-6B24FD3E-03FA-4B29-B85A-64EFF973A2C3Q30492977-C1DDDB5A-5464-4B68-AA7A-9B539274773AQ30502502-E27899A8-F570-4929-8A5F-16CAA4C15779Q30558412-6DF758F9-2E30-41D1-A2EC-163781843366Q33625221-AA082CBF-5CE1-4027-A709-01442C20BF43Q34085780-0A4F565A-78F1-4C09-93F4-662B220EA5A5Q34474321-26419622-B436-4AE1-A061-9CC58F7CF13BQ34494994-7A94EFA6-0561-4452-AB21-1CB414252A01Q34613667-E35920A1-233B-486E-9797-B4CEA2D778D0Q34727284-F275E50B-C47C-4E16-9B64-B971DF26AD2DQ34747375-2E8AA1B1-1601-4623-B87E-30F2FA3AF96CQ34883523-0494DD22-2406-475F-B86A-8C7D71232E60Q34974073-0746B5A4-7AC8-4CDD-8966-77A97FFA28D3Q35058184-ED6914F9-D432-4D04-B868-90E10DBDD0B5Q35085756-49BF0480-85AF-4AAB-89C7-5EA58A97A4F1Q35120600-6AC44933-03F5-46AF-A52F-9D297596A933Q35171068-D95C6259-4396-4EB1-A531-59DB54182DC2Q35360590-B9B2496E-2425-44A1-89F5-FFB39A85EBA5Q35537632-F355147D-F7A7-486A-8223-095FB49BC6D2Q35739938-3ED80488-7539-4853-A405-31D224F11567Q35925149-000CE3B2-E2F0-49D0-B585-3F0ABB17ED43Q35972599-0015A136-69E6-4F12-BA73-691747F118F6Q36000794-85488909-4FDE-446C-9EBD-C17BB795C8A2Q36068742-74518562-1677-4A63-A8D3-81117E2A3AC4Q36244730-D5446E53-91AD-4EAD-910D-B6B434026CA8Q36294966-68C337AF-60A6-4D25-ACB2-8755620FE741Q36397847-DAA7E66D-BE96-4C8D-872F-FECE306173BFQ36429192-16300054-CDE4-4B82-9ED7-391A90EE6F5EQ36486798-8B144C3A-88A7-4B37-BA6D-F6B98F02692EQ36585029-175F2AE1-C1DF-4313-A58D-6FEFD4002F7BQ36602836-FEDDFE98-6281-46DC-BB5A-1684D3DB2650Q36614746-DED25D80-5E77-42CF-B32A-9F1F571B5092Q36621452-1A618C37-CFA4-4422-B6A4-6A44C30E5D98Q36763034-93EFBFC6-AB48-4948-AE38-7686336C1A37Q36903452-F70D03E1-C9D2-4E59-A572-64D3F7226321Q37003285-1DBBE858-A64B-461D-A043-7D395038B406
P50
description
clinical geneticist and medical researcher
@en
hulumtuese
@sq
onderzoeker
@nl
հետազոտող
@hy
name
Ingrid Winship
@ast
Ingrid Winship
@en
Ingrid Winship
@es
Ingrid Winship
@sl
type
label
Ingrid Winship
@ast
Ingrid Winship
@en
Ingrid Winship
@es
Ingrid Winship
@sl
altLabel
Ingrid M Winship
@en
Ingrid Margaret Winship
@en
prefLabel
Ingrid Winship
@ast
Ingrid Winship
@en
Ingrid Winship
@es
Ingrid Winship
@sl
P1153
7003439648
P1280
P21
P27
P31
P496
0000-0001-8535-6003