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101. Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional Analyses

102. Characterization of an eutherian gene cluster generated after transposon domestication identifies Bex3 as relevant for advanced neurological functions

103. Genomic analysis of the natural history of attention-deficit/hyperactivity disorder using Neanderthal and ancient Homo sapiens samples

104. Cross-disorder genetic analyses implicate dopaminergic signaling as a biological link between adttention-eficit/hyperactivity disorder and obesity measures

105. Polygenic association between attention-deficit/hyperactivity disorder liability and cognitive impairments

110. Deficiency of the ywhazgene, involved in neurodevelopmental disorders, alters brain activity and behaviour in zebrafish

111. Utilidad del análisis del líquido cefalorraquídeo para el estudio de las deficiencias del metabolismo de neurotransmisores y pterinas y del transporte de glucosa y folato a través de la barrera hematoencefálica

112. Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome

116. Exploring DRD4 and its interaction with SLC6A3 as possible risk factors for adult ADHD: A meta-analysis in four European populations

118. Variants of the Aggression-Related RBFOX1 Gene in a Population Representative Birth Cohort Study: Aggressiveness, Personality, and Alcohol Use Disorder

120. Improved Diagnosis of Rare Disease Patients through Systematic Detection of Runs of Homozygosity

123. Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional Analyses

124. Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification

125. Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

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

128. Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping

129. Association of the PLCB1 gene with drug dependence

130. Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment

131. Genomic Relationships, Novel Loci, And Pleiotropic Mechanisms Across Eight Psychiatric Disorders

133. Migraine polygenic risk score associates with efficacy of migraine-specific drugs

134. Cross-disorder genetic analyses implicate dopaminergic signaling as a biological link between attention-deficit/hyperactivity disorder and obesity measures

138. A genetic investigation of sex bias in the prevalence of attention-deficit/hyperactivity disorder

144. Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment

148. CONVERGENT FUNCTIONAL GENOMICS APPROACH TO IDENTIFY GENES INVOLVED IN ATTENTION DEFICIT/HYPERACTIVITY DISORDER

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