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Katsuhito Yasuno

Katsuhito Yasuno,Yale University,Genetics & Genealogy,Neuroscience,Psychiatry & Psychology

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Katsuhito Yasuno

Yale University

Publications: 13 | Citations: 126

Fields: Genetics & Genealogy, Neuroscience, Psychiatry & Psychology

Collaborated with 187 co-authors from 2005 to 2011 | Cited by 769 authors

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Publications (13)

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Recessive LAMC3 mutations cause malformations of occipital cortical development

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Journal: Nature Genetics - NAT GENET , vol. 43, no. 6, pp. 590-594, 2011

Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations (Citations: 29)

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Journal: Nature , vol. 467, no. 7312, pp. 207-210, 2010

Genome-wide association study of intracranial aneurysm identifies three new risk loci (Citations: 12)

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Journal: Nature Genetics - NAT GENET , vol. 42, no. 5, pp. 420-425, 2010

L-Histidine Decarboxylase and Tourette's Syndrome (Citations: 7)

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Journal: New England Journal of Medicine - N ENGL J MED , vol. 362, no. 20, pp. 1901-1908, 2010

Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms (Citations: 1)

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Journal: Journal of Human Genetics - J HUM GENET , vol. 55, no. 10, pp. 656-661, 2010

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Citations (126 times by 118 publications)

The effects of a novel histamine-3 receptor inverse agonist on essential tremor in comparison to stable levels of alcohol

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Journal: Journal of Psychopharmacology - J PSYCHOPHARMACOL , vol. 26, no. 2, pp. 292-302, 2012

Statistical Guidance for Experimental Design and Data Analysis of Mutation Detection in Rare Monogenic Mendelian Diseases by Exome Sequencing

Journal: PLOS One , vol. 7, no. 2, 2012

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Co-authors (187)

Journals (10)

Keywords (44)

Katsuhito Yasuno,Yale University,Genetics & Genealogy,Neuroscience,Psychiatry & Psychology

Publications (13)

BibTeX | RIS | RefWorks Download

Recessive LAMC3 mutations cause malformations of occipital cortical development

Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations (Citations: 29)

Genome-wide association study of intracranial aneurysm identifies three new risk loci (Citations: 12)

L-Histidine Decarboxylase and Tourette's Syndrome (Citations: 7)

Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms (Citations: 1)

Citations (126 times by 118 publications)

The effects of a novel histamine-3 receptor inverse agonist on essential tremor in comparison to stable levels of alcohol

Whole-Exome Sequencing and Homozygosity Analysis Implicate Depolarization-Regulated Neuronal Genes in Autism

Intracranial Aneurysm Risk Locus 5q23.2 Is Associated with Elevated Systolic Blood Pressure

An Alu Element–Associated Hypermethylation Variant of the POMC Gene Is Associated with Childhood Obesity

Statistical Guidance for Experimental Design and Data Analysis of Mutation Detection in Rare Monogenic Mendelian Diseases by Exome Sequencing


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Katsuhito Yasuno,Yale University,Genetics & Genealogy,Neuroscience,Psychiatry & Psychology

Publications (13) BibTeX | RIS | RefWorks Download

Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations (Citations: 29)

Genome-wide association study of intracranial aneurysm identifies three new risk loci (Citations: 12)

L-Histidine Decarboxylase and Tourette's Syndrome (Citations: 7)

Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms (Citations: 1)

Publications (13)

BibTeX | RIS | RefWorks Download