Patrick Allard - Concepedia

Author

Patrick Allard

University of California, Los Angeles ORCID

Also Known As

Aaron Aday, Allard Patrick, Allard, Patrick, Camille L. Birch, Carlos A. Bacino, Daniel C. Dorset, David P. Bick, Diane B. Zastrow, Eva Baker, Janet S. Sinsheimer

112

Publications

3.4K

Citations

H-Index

Concepts

All Affiliations

University of California, Los Angeles Harvard University Baylor College of Medicine Columbia University Texas Children's Hospital

About

Patrick Allard is an author at University of California, Los Angeles specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	24	1.7K
2	Engineering	2	3	442
3	Health Sciences	2	2	68
4	Natural Sciences	2	2	204
5	Education	1	1	40

Patrick Allard

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome Julia Wang, Rami Al‐Ouran, Yanhui Hu, The American Journal of Human Genetics	2017	217
Diagnostic utility of transcriptome sequencing for rare Mendelian diseases Hane Lee, Alden Huang, Lee-kai Wang, Genetics in Medicine SequencingMendelian DisorderDiagnostic UtilityMedicineGenetics	2019	207
The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease Rachel Ramoni, John J. Mulvihill, David R. Adams, The American Journal of Human Genetics Disease DiagnosisNetwork ScienceHealth InformaticsData ScienceData Mining	2017	181
Bisphenol A impairs the double-strand break repair machinery in the germline and causes chromosome abnormalities Patrick Allard, Mónica P. Colaiácovo Proceedings of the National Academy of Sciences CytogeneticsBpa Exposure ResultsGeneticsGenomic MechanismMolecular Biology	2010	168
A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3 Hsiao‐Tuan Chao, Mariska Davids, Elizabeth A. Burke, The American Journal of Human Genetics Neurodevelopmental DisordersDevelopmental AnomalyDevelopmental BiologySyndromic Neurodevelopmental DisorderMendelian Disorder	2016	118
Exposure to the BPA-Substitute Bisphenol S Causes Unique Alterations of Germline Function Yichang Chen, Le Shu, Zhiqun Qiu, PLoS Genetics GeneticsMolecular GeneticsGenomicsReproductive BiologyEpigenetics	2016	108
IRF2BPL Is Associated with Neurological Phenotypes Paul C. Marcogliese, Vandana Shashi, Rebecca C. Spillmann, The American Journal of Human Genetics NeurologyNeuroscienceMolecular NeurobiologyNeuropathologyMedicine	2018	108
Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay Keren Machol, Justine Rousseau, Sophie Ehresmann, The American Journal of Human Genetics	2018	88
A <i>C. elegans</i> Screening Platform for the Rapid Assessment of Chemical Disruption of Germline Function Patrick Allard, Nicole Kleinstreuer, Thomas B. Knudsen, Environmental Health Perspectives	2013	86
De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype Vandana Shashi, Loren D.M. Peña, Katherine Kim, The American Journal of Human Genetics Allelic VariantSystems BiologySomatic VariantGenetic DisorderGenetics	2016	86

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