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New links to the pathogenesis of Crohn disease provided by genome-wide association scans

Nature reviews. Genetics, 2008-01, Vol.9 (1), p.9-14

Mathew, Christopher G

2008

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Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene

Nature genetics, 2010-05, Vol.42 (5), p.410-414

2010

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Mutation of the RAD51C gene in a Fanconi anemia-like disorder

Nature genetics, 2010-05, Vol.42 (5), p.406-409

2010

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Prevalence and Reclassification of Genetic Variants in South African Populations with Breast Cancer

Genes chromosomes & cancer, 2024-09, Vol.63 (9), p.e23275-n/a

2024

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A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1

Nature genetics, 2007-02, Vol.39 (2), p.207-211

2007

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Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer

Nature genetics, 2007-02, Vol.39 (2), p.162-164

2007

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Ranking lifestyle risk factors for cervical cancer among Black women: A case-control study from Johannesburg, South Africa

PloS one, 2021-12, Vol.16 (12), p.e0260319-e0260319

2021

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Genetic associations with carotid intima-media thickness link to atherosclerosis with sex-specific effects in sub-Saharan Africans

Nature communications, 2022-02, Vol.13 (1), p.855-855, Article 855

2022

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Esophageal Cancer Genomics in Africa: Recommendations for Future Research

Frontiers in genetics, 2022-03, Vol.13, p.864575-864575

2022

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A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M

Nature genetics, 2005-09, Vol.37 (9), p.958-963

2005

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The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J

Nature genetics, 2005-09, Vol.37 (9), p.934-935

2005

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Disruption of the Fanconi anemia-BRCA pathway in cisplatin-sensitive ovarian tumors

Nature medicine, 2003-05, Vol.9 (5), p.568-574

2003

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Systematic association mapping identifies NELL1 as a novel IBD disease gene

PloS one, 2007-08, Vol.2 (8), p.e691

2007

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The Relationship Between Environmental Exposure and Genetic Architecture of the 2q33 Locus With Esophageal Cancer in South Africa

Frontiers in genetics, 2019-05, Vol.10, p.406-406

2019

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The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease

Gastroenterology (New York, N.Y. 1943), 2002-04, Vol.122 (4), p.867-874

2002

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Novel and Known Gene-Smoking Interactions With cIMT Identified as Potential Drivers for Atherosclerosis Risk in West-African Populations of the AWI-Gen Study

Frontiers in genetics, 2020-02, Vol.10, p.1354-1354

2020

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HPV types 16/18 L1 E6 and E7 proteins seropositivity and cervical cancer risk in HIV-positive and HIV-negative black South African women

Infectious agents and cancer, 2022-03, Vol.17 (1), p.14-13, Article 14

2022

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Exome array analysis of adverse reactions to fluoropyrimidine-based therapy for gastrointestinal cancer

PloS one, 2018-05, Vol.13 (5), p.e0188911-e0188911

2018

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Association of a deletion of GSTT2B with an altered risk of oesophageal squamous cell carcinoma in a South African population: a case-control study

PloS one, 2011-12, Vol.6 (12), p.e29366

2011

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Interaction of FANCD2 and NBS1 in the DNA damage response

Nature cell biology, 2002-12, Vol.4 (12), p.913-920

2002

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Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes

Blood, 2004-04, Vol.103 (7), p.2498-2503

2004

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Genetic Susceptibility to Breast Cancer in Sub-Saharan African Populations

JCO global oncology, 2021-09, Vol.7 (7), p.1462-1471

2021

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Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci

BMC medical genetics, 2016-04, Vol.17 (1), p.26-26, Article 26

2016

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New links to the pathogenesis of Crohn disease provided by genome-wide association scans

Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene

Mutation of the RAD51C gene in a Fanconi anemia-like disorder

Prevalence and Reclassification of Genetic Variants in South African Populations with Breast Cancer

A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer

Ranking lifestyle risk factors for cervical cancer among Black women: A case-control study from Johannesburg, South Africa

Genetic associations with carotid intima-media thickness link to atherosclerosis with sex-specific effects in sub-Saharan Africans

Esophageal Cancer Genomics in Africa: Recommendations for Future Research

Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 ( IL17REL )

A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M

The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J

Disruption of the Fanconi anemia-BRCA pathway in cisplatin-sensitive ovarian tumors

Systematic association mapping identifies NELL1 as a novel IBD disease gene

The Relationship Between Environmental Exposure and Genetic Architecture of the 2q33 Locus With Esophageal Cancer in South Africa

The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease

Novel and Known Gene-Smoking Interactions With cIMT Identified as Potential Drivers for Atherosclerosis Risk in West-African Populations of the AWI-Gen Study

HPV types 16/18 L1 E6 and E7 proteins seropositivity and cervical cancer risk in HIV-positive and HIV-negative black South African women

Exome array analysis of adverse reactions to fluoropyrimidine-based therapy for gastrointestinal cancer

Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease

Association of a deletion of GSTT2B with an altered risk of oesophageal squamous cell carcinoma in a South African population: a case-control study

Interaction of FANCD2 and NBS1 in the DNA damage response

Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes

Genetic Susceptibility to Breast Cancer in Sub-Saharan African Populations

Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci

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