Bartha Maria Knoppers

Author

Also Known As

Amalia Issa, B M Knoppers, B. Knoppers, B. M. Knoppers, B. Maria Knoppers, B.M. Knoppers, BARTHA MARIA KNOPPERS, Bartha Knoppers, Bartha M Knoppers, Bartha M Knoppers*

717

Publications

77.7K

Citations

H-Index

330

Concepts

All Affiliations

McGill University Université de Montréal University of Toronto McGill Genome Centre University of Ottawa

About

Bartha Maria Knoppers is an author at McGill University specializing in medicine, research ethics, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	24	47	1.9K
2	Education	6	6	183
3	Health Sciences	4	4	82
4	Arts	1	1	46
5	Business	1	1	24

Bartha Maria Knoppers

222

Publications

18.5K

Citations

H-Index

Page 1

	Year	Citations
Pan-cancer analysis of whole genomes Lauri A. Aaltonen, Federico Abascal, Adam Abeshouse, Nature	2020	3.1K
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
A global reference for human genetic variation Adam Auton, Gonçalo R. Abecasis, David Altshuler, Civil War Book Review	2015	612
Comprehensive molecular characterization of mitochondrial genomes in human cancers Yuan Yuan, Young Seok Ju, Young-Wook Kim, Nature Genetics	2020	489
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel Olivier Delaneau, Jonathan Marchini, Gil McVean, Nature Communications Haplotype DeterminationNext-generation SequencingGeneticsGenomes ProjectArray Data	2014	441
Managing incidental findings and research results in genomic research involving biobanks and archived data sets Susan M. Wolf, Brittney N. Crock, Brian G. Van Ness, Genetics in Medicine Research ResultsIncidental FindingsBiobankGeneticsHigh Throughput Sequencing	2012	440
International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases Kym M. Boycott, Ana Rath, Jessica X. Chong, The American Journal of Human Genetics	2017	434
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge Catherine A. Brownstein, Alan H. Beggs, Nils Homer, Genome biology	2014	432
Whole-genome sequencing in health care Carla van El, Martina C. Cornel, Pascal Borry, European Journal of Human Genetics SequencingNext-generation SequencingGenomicsMedicineBioinformatics	2013	374
Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics. Carla van El, Martina C. Cornel, Pascal Borry, PubMed Whole-genome SequencingSequencingMedicineGeneticsNext-generation Sequencing	2013	356

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