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865 results on '"Mckay, James D"'

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103. A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma

105. Studying the Utility of Using Genetics to Predict Smoking-Related Outcomes in a Population-Based Study and a Selected Cohort

106. The PI3K/mTOR Pathway Is Targeted by Rare Germline Variants in Patients with Both Melanoma and Renal Cell Carcinoma

107. Transcriptome-wide association study reveals candidate causal genes for lung cancer

108. Mediating effect of soluble B-cell activation immune markers on the association between anthropometric and lifestyle factors and lymphoma development

110. Genome-wide association meta-analysis identifies pleiotropic risk loci for aerodigestive squamous cell cancers

111. Sequencing at lymphoid neoplasm susceptibility loci maps six myeloma risk genes

112. Assessing Lung Cancer Absolute Risk Trajectory Based on a Polygenic Risk Model

114. Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan Syndrome, including severe congenital cataract, dental anomalies, and mental retardation

115. Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls

117. The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma

118. Genome-Wide Association Study of Classical Hodgkin Lymphoma and Epstein–Barr Virus Status–Defined Subgroups

119. A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23

120. Genome-wide association study of HPV seropositivity

121. Association of a novel functional promoter variant (rs2075533 C>T) in the apoptosis gene TNFSF8 with risk of lung cancer—a finding from Texas lung cancer genome-wide association study

122. Patterns of Human Leukocyte Antigen Class I and Class II Associations and Cancer

123. Development of Sensitive Droplet Digital PCR Assays for Detecting Urinary TERT Promoter Mutations as Non-Invasive Biomarkers for Detection of Urothelial Cancer

124. Association between anthropometry and lifestyle factors and risk of B‐cell lymphoma: An exposome‐wide analysis

125. A molecular map of lung neuroendocrine neoplasms

126. Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology

127. Dissecting the genetic overlap of smoking behaviors, lung cancer, and chronic obstructive pulmonary disease: A focus on nicotinic receptors and nicotine metabolizing enzyme

128. The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls

129. Lipid Trait Variants and the Risk of Non-Hodgkin Lymphoma Subtypes: A Mendelian Randomization Study

130. Needlestack: an ultra-sensitive variant caller for multi-sample next generation sequencing data

131. Replication of Lung Cancer Susceptibility Loci at Chromosomes 15q25, 5p15, and 6p21: A Pooled Analysis From the International Lung Cancer Consortium

132. Association between a 15q25 gene variant, smoking quantity and tobacco-related cancers among 17 000 individuals

133. International Lung Cancer Consortium: Coordinated association study of 10 potential lung cancer susceptibility variants

138. Polymorphisms of genes coding for ghrelin and its receptor in relation to anthropometry, circulating levels of IGF-I and IGFBP-3, and breast cancer risk: a case–control study nested within the European Prospective Investigation into Cancer and Nutrition (EPIC)

139. A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25

140. Association of Polygenic Liabilities for Major Depression, Bipolar Disorder, and Schizophrenia With Risk for Depression in the Danish Population

141. Genome-wide association study identifies 30 loci associated with bipolar disorder

145. Genetic interaction analysis among oncogenesis-related genes revealed novel genes and networks in lung cancer development

146. Systematic analyses of regulatory variants in DNase I hypersensitive sites identified two novel lung cancer susceptibility loci

147. Elevated Platelet Count Appears to Be Causally Associated with Increased Risk of Lung Cancer : A Mendelian Randomization Analysis

148. Sex specific associations in genome wide association analysis of renal cell carcinoma

149. Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma.

150. Elevated platelet count appears to be causally associated with increased risk of lung cancer:A mendelian randomization analysis

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