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Annual Review of Biomedical Data Science
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September 1, 2021
Using Phecodes for Research with the Electronic Health Record: From PheWAS to PheRS
Lisa Bastarache
JAMA
|
May 17, 2022
Penetrance of Deleterious Clinical Variants
Lisa Bastarache, Josh F Peterson
Current Opinion in Ophthalmology
|
March 1, 2026
Opportunities and challenges in leveraging multiomics and biobanks for vision science
Dolly Ann Padovani-Claudio, Lisa Bastarache
Function (Oxford, England)
|
December 21, 2020
NKCC1: Newly Found as a Human Disease-Causing Ion Transporter
Rainelli Koumangoye, Lisa Bastarache, Eric Delpire
JAMIA Open
|
March 6, 2023
Linking rare and common disease vocabularies by mapping between the human phenotype ontology and phecodes
Evonne McArthur, Lisa Bastarache, John A Capra
Bioinformatics (Oxford, England)
|
September 9, 2022
The phers R package: using phenotype risk scores based on electronic health records to study Mendelian disease and rare genetic variants
Layla Aref, Lisa Bastarache, Jacob J Hughey
Medrxiv : the Preprint Server for Health Sciences
|
January 30, 2023
Phenotypic convergence: a novel phenomenon in the diagnostic process of Mendelian genetic disorders
Rory J Tinker, Josh Peterson, Lisa Bastarache
Genetics in Medicine : Official Journal of the American College of Medical Genetics
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June 20, 2023
Phenotypic presentation of Mendelian disease across the diagnostic trajectory in electronic health records
Rory J Tinker, Josh Peterson, Lisa Bastarache
American Journal of Clinical Pathology
|
October 13, 2021
Laboratory Predictors of Hemolytic Anemia in Patients With Systemic Loxoscelism
Jeremy W Jacobs, Lisa Bastarache, Mary Ann Thompson
The New England Journal of Medicine
|
April 4, 2019
Case 40-2018: A Woman with Recurrent Sinusitis, Cough, and Bronchiectasis
Lisa Bastarache, Julie A Bastarache, Joshua C Denny
Page
of 16
Search research articles
Search
Showing results (1-10 of 158) with videos related to
Sort By:
Page
of 16
Annual Review of Biomedical Data Science
|
September 1, 2021
Using Phecodes for Research with the Electronic Health Record: From PheWAS to PheRS
Lisa Bastarache
JAMA
|
May 17, 2022
Penetrance of Deleterious Clinical Variants
Lisa Bastarache, Josh F Peterson
Current Opinion in Ophthalmology
|
March 1, 2026
Opportunities and challenges in leveraging multiomics and biobanks for vision science
Dolly Ann Padovani-Claudio, Lisa Bastarache
Function (Oxford, England)
|
December 21, 2020
NKCC1: Newly Found as a Human Disease-Causing Ion Transporter
Rainelli Koumangoye, Lisa Bastarache, Eric Delpire
JAMIA Open
|
March 6, 2023
Linking rare and common disease vocabularies by mapping between the human phenotype ontology and phecodes
Evonne McArthur, Lisa Bastarache, John A Capra
Bioinformatics (Oxford, England)
|
September 9, 2022
The phers R package: using phenotype risk scores based on electronic health records to study Mendelian disease and rare genetic variants
Layla Aref, Lisa Bastarache, Jacob J Hughey
Medrxiv : the Preprint Server for Health Sciences
|
January 30, 2023
Phenotypic convergence: a novel phenomenon in the diagnostic process of Mendelian genetic disorders
Rory J Tinker, Josh Peterson, Lisa Bastarache
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 20, 2023
Phenotypic presentation of Mendelian disease across the diagnostic trajectory in electronic health records
Rory J Tinker, Josh Peterson, Lisa Bastarache
American Journal of Clinical Pathology
|
October 13, 2021
Laboratory Predictors of Hemolytic Anemia in Patients With Systemic Loxoscelism
Jeremy W Jacobs, Lisa Bastarache, Mary Ann Thompson
The New England Journal of Medicine
|
April 4, 2019
Case 40-2018: A Woman with Recurrent Sinusitis, Cough, and Bronchiectasis
Lisa Bastarache, Julie A Bastarache, Joshua C Denny
Page
of 16