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1
Association analyses based on false discovery rate implicate new loci for coronary artery disease
Association analyses based on false discovery rate implicate new loci for coronary artery disease
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Association analyses based on false discovery rate implicate new loci for coronary artery disease

Nature genetics, 2017-09, Vol.49 (9), p.1385-1391 [Peer Reviewed Journal]

COPYRIGHT 2017 Nature Publishing Group ;COPYRIGHT 2017 Nature Publishing Group ;Copyright Nature Publishing Group Sep 2017 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.3913 ;PMID: 28714975

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2
The Human Phenotype Ontology in 2017
The Human Phenotype Ontology in 2017
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The Human Phenotype Ontology in 2017

Nucleic acids research, 2017-01, Vol.45 (D1), p.D865-D876 [Peer Reviewed Journal]

The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. ;Distributed under a Creative Commons Attribution 4.0 International License ;The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. 2017 ;ISSN: 0305-1048 ;EISSN: 1362-4962 ;DOI: 10.1093/nar/gkw1039 ;PMID: 27899602

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3
Multi-trait analysis of genome-wide association summary statistics using MTAG
Multi-trait analysis of genome-wide association summary statistics using MTAG
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Multi-trait analysis of genome-wide association summary statistics using MTAG

Nature genetics, 2018-02, Vol.50 (2), p.229-237 [Peer Reviewed Journal]

COPYRIGHT 2018 Nature Publishing Group ;COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Feb 2018 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-017-0009-4 ;PMID: 29292387

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4
Association of Genetic and Environmental Factors With Autism in a 5-Country Cohort
Association of Genetic and Environmental Factors With Autism in a 5-Country Cohort
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Association of Genetic and Environmental Factors With Autism in a 5-Country Cohort

JAMA psychiatry (Chicago, Ill.), 2019-10, Vol.76 (10), p.1035 [Peer Reviewed Journal]

ISSN: 2168-6238 ;EISSN: 2168-6238 ;DOI: 10.1001/jamapsychiatry.2019.1411

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5
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test
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Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test

Genetics in medicine, 2018-04, Vol.20 (4), p.435-443 [Peer Reviewed Journal]

Copyright Nature Publishing Group Apr 2018 ;Copyright © 2018 The Author(s) 2018 The Author(s) ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2017.119 ;PMID: 28771251

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6
Genome-wide genetic marker discovery and genotyping using next-generation sequencing
Genome-wide genetic marker discovery and genotyping using next-generation sequencing
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Genome-wide genetic marker discovery and genotyping using next-generation sequencing

Nature reviews. Genetics, 2011-07, Vol.12 (7), p.499-510 [Peer Reviewed Journal]

2015 INIST-CNRS ;COPYRIGHT 2011 Nature Publishing Group ;COPYRIGHT 2011 Nature Publishing Group ;Copyright Nature Publishing Group Jul 2011 ;ISSN: 1471-0056 ;EISSN: 1471-0064 ;DOI: 10.1038/nrg3012 ;PMID: 21681211

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7
A framework for an evidence-based gene list relevant to autism spectrum disorder
A framework for an evidence-based gene list relevant to autism spectrum disorder
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A framework for an evidence-based gene list relevant to autism spectrum disorder

Nature reviews. Genetics, 2020-06, Vol.21 (6), p.367-376 [Peer Reviewed Journal]

COPYRIGHT 2020 Nature Publishing Group ;Springer Nature Limited 2020. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1471-0056 ;EISSN: 1471-0064 ;DOI: 10.1038/s41576-020-0231-2 ;PMID: 32317787

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8
The Genetic Architecture of Gene Expression in Peripheral Blood
The Genetic Architecture of Gene Expression in Peripheral Blood
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The Genetic Architecture of Gene Expression in Peripheral Blood

American journal of human genetics, 2017-02, Vol.100 (2), p.228-237 [Peer Reviewed Journal]

2017 American Society of Human Genetics ;Copyright © 2017 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Feb 2, 2017 ;2016 American Society of Human Genetics. 2017 American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2016.12.008 ;PMID: 28065468

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9
Computational tools for prioritizing candidate genes: boosting disease gene discovery
Computational tools for prioritizing candidate genes: boosting disease gene discovery
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Computational tools for prioritizing candidate genes: boosting disease gene discovery

Nature reviews. Genetics, 2012-08, Vol.13 (8), p.523-536 [Peer Reviewed Journal]

2015 INIST-CNRS ;COPYRIGHT 2012 Nature Publishing Group ;COPYRIGHT 2012 Nature Publishing Group ;Copyright Nature Publishing Group Aug 2012 ;ISSN: 1471-0056 ;EISSN: 1471-0064 ;DOI: 10.1038/nrg3253 ;PMID: 22751426

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10
Analysing and interpreting DNA methylation data
Analysing and interpreting DNA methylation data
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Analysing and interpreting DNA methylation data

Nature reviews. Genetics, 2012-10, Vol.13 (10), p.705-719 [Peer Reviewed Journal]

2015 INIST-CNRS ;COPYRIGHT 2012 Nature Publishing Group ;COPYRIGHT 2012 Nature Publishing Group ;Copyright Nature Publishing Group Oct 2012 ;ISSN: 1471-0056 ;EISSN: 1471-0064 ;DOI: 10.1038/nrg3273 ;PMID: 22986265

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11
Beyond SNP heritability: Polygenicity and discoverability of phenotypes estimated with a univariate Gaussian mixture model
Beyond SNP heritability: Polygenicity and discoverability of phenotypes estimated with a univariate Gaussian mixture model
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Beyond SNP heritability: Polygenicity and discoverability of phenotypes estimated with a univariate Gaussian mixture model

PLoS genetics, 2020-05, Vol.16 (5), p.e1008612-e1008612 [Peer Reviewed Journal]

COPYRIGHT 2020 Public Library of Science ;COPYRIGHT 2020 Public Library of Science ;2020 Holland et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;info:eu-repo/semantics/openAccess ;2020 Holland et al 2020 Holland et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1008612 ;PMID: 32427991

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12
Next-generation phenotyping: requirements and strategies for enhancing our understanding of genotype–phenotype relationships and its relevance to crop improvement
Next-generation phenotyping: requirements and strategies for enhancing our understanding of genotype–phenotype relationships and its relevance to crop improvement
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Next-generation phenotyping: requirements and strategies for enhancing our understanding of genotype–phenotype relationships and its relevance to crop improvement

Theoretical and applied genetics, 2013-04, Vol.126 (4), p.867-887 [Peer Reviewed Journal]

The Author(s) 2013 ;COPYRIGHT 2013 Springer ;Springer-Verlag Berlin Heidelberg 2013 ;ISSN: 0040-5752 ;EISSN: 1432-2242 ;DOI: 10.1007/s00122-013-2066-0 ;PMID: 23471459

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13
Balancing scientific interests and the rights of participants in designing a recall by genotype study
Balancing scientific interests and the rights of participants in designing a recall by genotype study
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Balancing scientific interests and the rights of participants in designing a recall by genotype study

European journal of human genetics : EJHG, 2021-07, Vol.29 (7), p.1146-1157 [Peer Reviewed Journal]

2021. The Author(s). ;The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 1018-4813 ;ISSN: 1476-5438 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-021-00860-7 ;PMID: 33981014

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14
Origins of human genetics. A personal perspective
Origins of human genetics. A personal perspective
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Origins of human genetics. A personal perspective

European journal of human genetics : EJHG, 2021-07, Vol.29 (7), p.1038-1044 [Peer Reviewed Journal]

2020. The Author(s). ;The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-020-00785-7 ;PMID: 33542497

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15
Benefits and limitations of genome-wide association studies
Benefits and limitations of genome-wide association studies
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Benefits and limitations of genome-wide association studies

Nature reviews. Genetics, 2019-08, Vol.20 (8), p.467-484 [Peer Reviewed Journal]

COPYRIGHT 2019 Nature Publishing Group ;COPYRIGHT 2019 Nature Publishing Group ;Springer Nature Limited 2019. ;ISSN: 1471-0056 ;EISSN: 1471-0064 ;DOI: 10.1038/s41576-019-0127-1 ;PMID: 31068683

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16
A compendium of mutational cancer driver genes
A compendium of mutational cancer driver genes
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A compendium of mutational cancer driver genes

Nature reviews. Cancer, 2020-10, Vol.20 (10), p.555-572 [Peer Reviewed Journal]

COPYRIGHT 2020 Nature Publishing Group ;Springer Nature Limited 2020. ;ISSN: 1474-175X ;EISSN: 1474-1768 ;DOI: 10.1038/s41568-020-0290-x ;PMID: 32778778

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17
Searching for secondary findings: considering actionability and preserving the right not to know
Searching for secondary findings: considering actionability and preserving the right not to know
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Searching for secondary findings: considering actionability and preserving the right not to know

European journal of human genetics : EJHG, 2019-10, Vol.27 (10), p.1481-1484 [Peer Reviewed Journal]

The Author(s), under exclusive licence to European Society of Human Genetics 2019. ;Distributed under a Creative Commons Attribution 4.0 International License ;The Author(s), under exclusive licence to European Society of Human Genetics 2019 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/s41431-019-0438-x ;PMID: 31186543

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18
Prioritization of neurodevelopmental disease genes by discovery of new mutations
Prioritization of neurodevelopmental disease genes by discovery of new mutations
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Prioritization of neurodevelopmental disease genes by discovery of new mutations

Nature neuroscience, 2014-06, Vol.17 (6), p.764-772 [Peer Reviewed Journal]

COPYRIGHT 2014 Nature Publishing Group ;COPYRIGHT 2014 Nature Publishing Group ;Copyright Nature Publishing Group Jun 2014 ;ISSN: 1097-6256 ;EISSN: 1546-1726 ;DOI: 10.1038/nn.3703 ;PMID: 24866042 ;CODEN: NANEFN

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19
Accelerating Discovery of Functional Mutant Alleles in Cancer
Accelerating Discovery of Functional Mutant Alleles in Cancer
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Accelerating Discovery of Functional Mutant Alleles in Cancer

Cancer discovery, 2018-02, Vol.8 (2), p.174-183

2017 American Association for Cancer Research. ;ISSN: 2159-8274 ;EISSN: 2159-8290 ;DOI: 10.1158/2159-8290.cd-17-0321 ;PMID: 29247016

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20
FlyBase at 25: looking to the future
FlyBase at 25: looking to the future
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FlyBase at 25: looking to the future

Nucleic acids research, 2017-01, Vol.45 (D1), p.D663-D671 [Peer Reviewed Journal]

The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. ;The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. 2017 ;ISSN: 0305-1048 ;EISSN: 1362-4962 ;DOI: 10.1093/nar/gkw1016 ;PMID: 27799470

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