Pages that link to "Q88355788"

The following pages link to Sara E Dobbins (Q88355788):

Displaying 26 items.

• Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer (Q21144952) (← links)
• Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas (Q24617520) (← links)
• Correspondence: SEMA4A variation and risk of colorectal cancer (Q28602609) (← links)
• Common variation at 10p12.31 near MLLT10 influences meningioma risk (Q28943376) (← links)
• Chromosome 7p11.2 (EGFR) variation influences glioma risk (Q28943530) (← links)
• Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33 (Q29417032) (← links)
• Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk (Q29417133) (← links)
• CanVar: A resource for sharing germline variation in cancer patients (Q30490732) (← links)
• Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis (Q34048230) (← links)
• Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genes (Q35056061) (← links)
• A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer (Q35626744) (← links)
• Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer. (Q36058262) (← links)
• Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer (Q36265886) (← links)
• Deciphering the 8q24.21 association for glioma (Q36839027) (← links)
• Undefined familial colorectal cancer and the role of pleiotropism in cancer susceptibility genes (Q37231035) (← links)
• Deciphering the genetic architecture of low-penetrance susceptibility to colorectal cancer (Q37332239) (← links)
• Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk (Q37659388) (← links)
• Validation of Recently Proposed Colorectal Cancer Susceptibility Gene Variants in an Analysis of Families and Patients-a Systematic Review (Q38974107) (← links)
• Genetic Predisposition to Multiple Myeloma at 5q15 Is Mediated by an ELL2 Enhancer Polymorphism (Q40043371) (← links)
• Erratum: A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer (Q42412214) (← links)
• Allergy and glioma risk: test of association by genotype. (Q48185601) (← links)
• Whole-genome sequencing of multiple myeloma reveals oncogenic pathways are targeted somatically through multiple mechanisms. (Q52321832) (← links)
• Genetic diagnosis of high-penetrance susceptibility for colorectal cancer (CRC) is achievable for a high proportion of familial CRC by exome sequencing. (Q54275718) (← links)
• Genome-wide association analysis identifies a meningioma risk locus at 11p15.5 (Q56375615) (← links)
• Identification of recurrent noncoding mutations in B-cell lymphoma using capture Hi-C (Q60921239) (← links)
• Promoter capture Hi-C-based identification of recurrent noncoding mutations in colorectal cancer (Q61876944) (← links)