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126 results on '"Whelan, Christopher D."'

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101. Novel genetic loci underlying human intracranial volume identified through genome-wide association

102. Novel genetic loci underlying human intracranial volume identified through genome-wide association

104. Common genetic variants influence human subcortical brain structures

105. Smaller hippocampal CA1 subfield volume in posttraumatic stress disorder.

106. Common variants at 12q14 and 12q24 are associated with hippocampal volume

109. Dynamics of Brain Structure and its Genetic Architecture over the Lifespan

110. Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept

111. Dynamics of Brain Structure and its Genetic Architecture over the Lifespan

112. Analysis of shared heritability in common disorders of the brain

113. Analysis of shared heritability in common disorders of the brain

114. Analysis of shared heritability in common disorders of the brain

115. Analysis of shared heritability in common disorders of the brain

116. Proteogenomic network analysis reveals dysregulated mechanisms and potential mediators in Parkinson's disease.

117. A WORLDWIDE ENIGMA STUDY ON EPILEPSY-RELATED GRAY AND WHITE MATTER COMPROMISE ACROSS THE ADULT LIFESPAN.

118. Genome-Wide Association Studies of ARIA From the Aducanumab Phase 3 ENGAGE and EMERGE Studies.

119. Plasma proteomic associations with genetics and health in the UK Biobank.

120. Rare variant associations with plasma protein levels in the UK Biobank.

121. Event-based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross-sectional data.

122. Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy.

123. Genetic variants associated with longitudinal changes in brain structure across the lifespan.

124. A systems-level analysis highlights microglial activation as a modifying factor in common epilepsies.

125. ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries.

126. Analysis of shared heritability in common disorders of the brain.

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