Bhooma Thiruvahindrapuram

Author

Also Known As

B Thiruvahindrapuram, B. Thiruvahindrapuram, Bhooma Thiruv, Bhooma Thiruvahindrapuram, Daniel P Howrigan, Guo K, Omar Shanta, Scott, Rodney J., Shelley Bull, Thiruvahindrapuram Bhooma

168

Publications

10.7K

Citations

H-Index

Concepts

All Affiliations

University of Toronto Hospital for Sick Children SickKids Foundation Holland Bloorview Kids Rehabilitation Hospital Centre for Addiction and Mental Health

About

Bhooma Thiruvahindrapuram is an author at University of Toronto specializing in genetics, medicine, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	15	4.5K
2	Engineering	2	2	909
3	Public Health	2	2	371
4	Social Sciences	2	2	186
5	Biostatistics	1	1	200

Bhooma Thiruvahindrapuram

Publications

10.4K

Citations

H-Index

Page 1

	Year	Citations
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects Christian R. Marshall, Daniel P. Howrigan, Daniele Merico, Nature Genetics PsychiatryGeneticsPsychiatric GeneticsGenetic EpidemiologyCopy Number Variants	2016	1.1K
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders Dalila Pinto, Elsa Delaby, Daniele Merico, The American Journal of Human Genetics	2014	1K
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder Ryan K. C. Yuen, Daniele Merico, Matt Bookman, Nature Neuroscience Next-generation SequencingGeneticsPsychiatric GeneticsMolecular BiologyAutism	2017	910
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test Anath C. Lionel, Gregory Costain, Nasim Monfared, Genetics in Medicine	2017	551
Whole-genome sequencing of quartet families with autism spectrum disorder Ryan K. C. Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, Nature Medicine SequencingSyndromic AutismNext-generation SequencingGeneticsMolecular Biology	2015	540
Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing Yong‐hui Jiang, Ryan K. C. Yuen, Xin Jin, The American Journal of Human Genetics Whole-genome SequencingSequencingEngineeringVariant InterpretationMedicine	2013	491
Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder Kristiina Tammimies, Christian R. Marshall, Susan Walker, JAMA	2015	432
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants Dalila Pinto, Katayoon Darvishi, Xinghua Shi, Nature Biotechnology Hardware SecurityComprehensive AssessmentEngineeringContent Similarity DetectionData Science	2011	418
Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD Anath C. Lionel, Jennifer Crosbie, Nicole Barbosa, Science Translational Medicine	2011	385
Whole-genome sequencing expands diagnostic utility and improves clinical management in paediatric medicine Dimitri J. Stavropoulos, Daniele Merico, Rebekah Jobling, npj Genomic Medicine	2016	374

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