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Benjamin M Neale

Showing results (201-210 of 293) with videos related to

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Neuron|September 7, 2018
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 FamiliesPadhraig Gormley, Mitja I Kurki, Marjo Eveliina Hiekkala, et al.
Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.
Neuron|May 8, 2018
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 FamiliesPadhraig Gormley, Mitja I Kurki, Marjo Eveliina Hiekkala, et al.
Human Molecular Genetics|November 11, 2008
Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degenerationClaire L Simpson, Robin Lemmens, Katarzyna Miskiewicz, et al.
Science (New York, N.Y.)|December 15, 2018
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorderJoon-Yong An, Kevin Lin, Lingxue Zhu, et al.
Nature Neuroscience|November 27, 2019
Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock proteinSali M K Farhan, Daniel P Howrigan, Liam E Abbott, et al.
Nature Neuroscience|February 9, 2016
Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of conceptBarbara Franke, Jason L Stein, Stephan Ripke, et al.
Nature Communications|August 25, 2018
Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestriesSeyedeh M Zekavat, Sanni Ruotsalainen, Robert E Handsaker, et al.
Nature Communications|April 3, 2020
Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestriesSeyedeh M Zekavat, Sanni Ruotsalainen, Robert E Handsaker, et al.
Nature|October 15, 2020
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cellsErik L Bao, Satish K Nandakumar, Xiaotian Liao, et al.
Pageof 30

Showing results (201-210 of 293) with videos related to

Sort By:
Pageof 30
Neuron|September 7, 2018
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 FamiliesPadhraig Gormley, Mitja I Kurki, Marjo Eveliina Hiekkala, et al.
Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.
Neuron|May 8, 2018
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 FamiliesPadhraig Gormley, Mitja I Kurki, Marjo Eveliina Hiekkala, et al.
Human Molecular Genetics|November 11, 2008
Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degenerationClaire L Simpson, Robin Lemmens, Katarzyna Miskiewicz, et al.
Science (New York, N.Y.)|December 15, 2018
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorderJoon-Yong An, Kevin Lin, Lingxue Zhu, et al.
Nature Neuroscience|November 27, 2019
Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock proteinSali M K Farhan, Daniel P Howrigan, Liam E Abbott, et al.
Nature Neuroscience|February 9, 2016
Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of conceptBarbara Franke, Jason L Stein, Stephan Ripke, et al.
Nature Communications|August 25, 2018
Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestriesSeyedeh M Zekavat, Sanni Ruotsalainen, Robert E Handsaker, et al.
Nature Communications|April 3, 2020
Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestriesSeyedeh M Zekavat, Sanni Ruotsalainen, Robert E Handsaker, et al.
Nature|October 15, 2020
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cellsErik L Bao, Satish K Nandakumar, Xiaotian Liao, et al.
Pageof 30