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Journal of Law and the Biosciences
|
October 16, 2014
Newborn screening in the genomics era
Shannon Rego
Journal of Bioethical Inquiry
|
August 25, 2023
The Need to Standardize the Reanalysis of Genomic Sequencing Results: Findings from Interviews with Underserved Families in Genomic Research
Simon M Outram, Shannon Rego, Matthew Norstad, et al.
Cold Spring Harbor Perspectives in Medicine
|
October 2, 2019
Informed Consent in the Genomics Era
Shannon Rego, Megan E Grove, Mildred K Cho, et al.
Human Genetics
|
March 31, 2022
Predicting genes from phenotypes using human phenotype ontology (HPO) terms
Anne Slavotinek, Hannah Prasad, Tiffany Yip, et al.
Journal of Genetic Counseling
|
March 6, 2019
Much ado about nothing: A qualitative study of the experiences of an average-risk population receiving results of exome sequencing
Shannon Rego, Orit Dagan-Rosenfeld, Stephanie A Bivona, et al.
American Journal of Medical Genetics. Part A
|
September 9, 2020
The expanding spectrum of NFIB-associated phenotypes in a diverse patient population-A report of two new patients
Kathleen Barrus, Shannon Rego, Tiffany Yip, et al.
American Journal of Medical Genetics. Part A
|
August 30, 2019
Developmental and epileptic encephalopathy in two siblings with a novel, homozygous missense variant in SCN1B
Natasha Darras, Thoa K Ha, Shannon Rego, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 5, 2017
A Case Report of Hypoglycemia and Hypogammaglobulinemia: DAVID Syndrome in a Patient With a Novel NFKB2 Mutation
Rayhan A Lal, Laura K Bachrach, Andrew R Hoffman, et al.
Orphanet Journal of Rare Diseases
|
July 7, 2025
Characterizing healthcare resource utilization in two rare diseases (Kleefstra syndrome and SLC6A1 epileptic encephalopathy) using multimodal real-world data
Caitlin A Nichols, Ella Nysetvold, Mike Jackson, et al.
Obstetrics and Gynecology
|
July 25, 2024
Cell-Free DNA Analysis for the Determination of Fetal Red Blood Cell Antigen Genotype in Individuals With Alloimmunized Pregnancies
Shannon Rego, Olaide Ashimi Balogun, Kirsten Emanuel, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 32) with videos related to
Sort By:
Page
of 4
Journal of Law and the Biosciences
|
October 16, 2014
Newborn screening in the genomics era
Shannon Rego
Journal of Bioethical Inquiry
|
August 25, 2023
The Need to Standardize the Reanalysis of Genomic Sequencing Results: Findings from Interviews with Underserved Families in Genomic Research
Simon M Outram, Shannon Rego, Matthew Norstad, et al.
Cold Spring Harbor Perspectives in Medicine
|
October 2, 2019
Informed Consent in the Genomics Era
Shannon Rego, Megan E Grove, Mildred K Cho, et al.
Human Genetics
|
March 31, 2022
Predicting genes from phenotypes using human phenotype ontology (HPO) terms
Anne Slavotinek, Hannah Prasad, Tiffany Yip, et al.
Journal of Genetic Counseling
|
March 6, 2019
Much ado about nothing: A qualitative study of the experiences of an average-risk population receiving results of exome sequencing
Shannon Rego, Orit Dagan-Rosenfeld, Stephanie A Bivona, et al.
American Journal of Medical Genetics. Part A
|
September 9, 2020
The expanding spectrum of NFIB-associated phenotypes in a diverse patient population-A report of two new patients
Kathleen Barrus, Shannon Rego, Tiffany Yip, et al.
American Journal of Medical Genetics. Part A
|
August 30, 2019
Developmental and epileptic encephalopathy in two siblings with a novel, homozygous missense variant in SCN1B
Natasha Darras, Thoa K Ha, Shannon Rego, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 5, 2017
A Case Report of Hypoglycemia and Hypogammaglobulinemia: DAVID Syndrome in a Patient With a Novel NFKB2 Mutation
Rayhan A Lal, Laura K Bachrach, Andrew R Hoffman, et al.
Orphanet Journal of Rare Diseases
|
July 7, 2025
Characterizing healthcare resource utilization in two rare diseases (Kleefstra syndrome and SLC6A1 epileptic encephalopathy) using multimodal real-world data
Caitlin A Nichols, Ella Nysetvold, Mike Jackson, et al.
Obstetrics and Gynecology
|
July 25, 2024
Cell-Free DNA Analysis for the Determination of Fetal Red Blood Cell Antigen Genotype in Individuals With Alloimmunized Pregnancies
Shannon Rego, Olaide Ashimi Balogun, Kirsten Emanuel, et al.
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of 4