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Author Details

Noura S Abul-Husn
Institute for Genomic Health, Icahn School of Medicine at Mount Sinai
2002
66
28
PMIDPaper TitleJournal TitlePublished Year
37897232Physician services and costs after disclosure of diagnostic sequencing results in the NYCKidSeq program.Genet Med2024
37897232Physician services and costs after disclosure of diagnostic sequencing results in the NYCKidSeq program.Genet Med2024
36372942Prescriber Adoption of SLCO1B1 Genotype-Guided Simvastatin Clinical Decision Support in a Clinical Pharmacogenetics Program.Clin Pharmacol Ther2023
36372942Prescriber Adoption of SLCO1B1 Genotype-Guided Simvastatin Clinical Decision Support in a Clinical Pharmacogenetics Program.Clin Pharmacol Ther2023
37600667Admixture mapping of peripheral artery disease in a Dominican population reveals a putative risk locus on 2q35.Front Genet2023
38006881The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic results disclosure in diverse families.Am J Hum Genet2023
38084291Specifications of the ACMG/AMP Variant Classification Guidelines for Germline <i>DICER1</i> Variant Curation.Hum Mutat2023
38054855Pharmacogenomic knowledge and awareness among diverse patients treated with angiotensin converting enzyme inhibitors.Pharmacogenomics2023
37347242ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG).Genet Med2023
37158195Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients.Genet Med2023
37334874Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program.Clin Genet2023
37461450The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic counseling in racially and ethnically diverse families.medRxiv2023
36575824Elective genetic testing: Genetics professionals' perspectives and practices.J Genet Couns2023
36949526The TeleKidSeq pilot study: incorporating telehealth into clinical care of children from diverse backgrounds undergoing whole genome sequencing.Pilot Feasibility Stud2023
36563179Detection of mosaic variants using genome sequencing in a large pediatric cohort.Am J Med Genet A2023
36549199Diverse and unselected adults with clinically relevant ACADS variants lack evidence of metabolic disease.Mol Genet Metab2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
36610497Association of HSD17B13 and PNPLA3 With Liver Enzymes and Fibrosis in Hispanic/Latino Individuals of Diverse Genetic Ancestries.Clin Gastroenterol Hepatol2023
36993157Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients.medRxiv2023
36607395TTR Val142Ile: Bystander Genetic Finding or Diagnosis?Pediatr Cardiol2023
37034679Admixture Mapping of Peripheral Artery Disease in a Dominican Population Reveals a Novel Risk Locus on 2q35.medRxiv2023
38084291Specifications of the ACMG/AMP Variant Classification Guidelines for Germline <i>DICER1</i> Variant Curation.Hum Mutat2023
38006881The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic results disclosure in diverse families.Am J Hum Genet2023
38054855Pharmacogenomic knowledge and awareness among diverse patients treated with angiotensin converting enzyme inhibitors.Pharmacogenomics2023
37600667Admixture mapping of peripheral artery disease in a Dominican population reveals a putative risk locus on 2q35.Front Genet2023
37461450The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic counseling in racially and ethnically diverse families.medRxiv2023
37158195Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients.Genet Med2023
36993157Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients.medRxiv2023
36949526The TeleKidSeq pilot study: incorporating telehealth into clinical care of children from diverse backgrounds undergoing whole genome sequencing.Pilot Feasibility Stud2023
37347242ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG).Genet Med2023
37334874Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program.Clin Genet2023
37034679Admixture Mapping of Peripheral Artery Disease in a Dominican Population Reveals a Novel Risk Locus on 2q35.medRxiv2023
36549199Diverse and unselected adults with clinically relevant ACADS variants lack evidence of metabolic disease.Mol Genet Metab2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
36610497Association of HSD17B13 and PNPLA3 With Liver Enzymes and Fibrosis in Hispanic/Latino Individuals of Diverse Genetic Ancestries.Clin Gastroenterol Hepatol2023
36575824Elective genetic testing: Genetics professionals' perspectives and practices.J Genet Couns2023
36607395TTR Val142Ile: Bystander Genetic Finding or Diagnosis?Pediatr Cardiol2023
36563179Detection of mosaic variants using genome sequencing in a large pediatric cohort.Am J Med Genet A2023
33886068CDH1 pathogenic variants and cancer risk in an unselected patient population.Fam Cancer2022
35710995Genome-wide polygenic score to predict chronic kidney disease across ancestries.Nat Med2022
35380538Perspectives of diverse Spanish- and English-speaking patients on the clinical use of polygenic risk scores.Genet Med2022
35802134ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG).Genet Med2022
35672798Addressing the routine failure to clinically identify monogenic cases of common disease.Genome Med2022
33886068CDH1 pathogenic variants and cancer risk in an unselected patient population.Fam Cancer2022
35710995Genome-wide polygenic score to predict chronic kidney disease across ancestries.Nat Med2022
35802134ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG).Genet Med2022
35380538Perspectives of diverse Spanish- and English-speaking patients on the clinical use of polygenic risk scores.Genet Med2022
35672798Addressing the routine failure to clinically identify monogenic cases of common disease.Genome Med2022
33467513Genomic Screening Identifies Individuals at High Risk for Hereditary Transthyretin Amyloidosis.J Pers Med2021
34180972Association Between a Common, Benign Genotype and Unnecessary Bone Marrow Biopsies Among African American Patients.JAMA Intern Med2021
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Collaborators

Eimear E Kenny
Icahn School of Medicine at Mount Sinai, NY Institute for Genomic Health
Co-authored papers 30
Sabrina A Suckiel
Icahn School of Medicine at Mount Sinai
Co-authored papers 18
Carol R Horowitz
Institute for Health Equity Research, Icahn School of Medicine at Mount Sinai
Co-authored papers 13
John M Greally
Co-authored papers 10
Omri Gottesman
Icahn School of Medicine at Mount Sinai
Co-authored papers 10
Emily R Soper
Institute for Genomic Health, Icahn School of Medicine at Mount Sinai
Co-authored papers 10
Bruce D Gelb
Icahn School of Medicine at Mount Sinai
Co-authored papers 9
Erwin P Bottinger
Hasso Plattner Institute for Digital Health at Mount Sinai
Co-authored papers 9
Michael F Murray
Yale School of Medicine
Co-authored papers 8
Marylyn D Ritchie
Center for Systems Genomics, Pennsylvania State University, University Park
Co-authored papers 8
Judy H Cho
Co-authored papers 8
David J Carey
Geisinger Medical Center
Co-authored papers 7
Ruth J F Loos
Co-authored papers 7
Lakshmi A Devi
Co-authored papers 6
Marc S Williams
University of Washington Medical Center
Co-authored papers 6
Frederick E Dewey
Co-authored papers 6
Aniwaa Owusu Obeng
Icahn School of Medicine at Mount Sinai
Co-authored papers 6
Aris Baras
Co-authored papers 5
David H Ledbetter
University of Florida, College of Medicine-Jacksonville
Co-authored papers 5
Stuart A Scott
Stanford University
Co-authored papers 5
John D Overton
Regeneron Pharmaceuticals
Co-authored papers 5
Stephen B Ellis
Icahn School of Medicine at Mount Sinai
Co-authored papers 5
Scott M Damrauer
Perelman School of Medicine, University of Pennsylvania
Co-authored papers 4
Kandamurugu Manickam
Nationwide Children's Hospital, The Ohio State University College of Medicine
Co-authored papers 4
Bart S Ferket
Institute for Healthcare Delivery Science, Icahn School of Medicine at Mount Sinai
Co-authored papers 4
Adam S Gordon
Northwestern University Feinberg School of Medicine.
Co-authored papers 4
Wendy K Chung
Boston Children's Hospital, Harvard Medical School
Co-authored papers 4
Joshua C Denny
Vanderbilt University
Co-authored papers 4
Matthew S Lebo
Harvard Medical School, Brigham and Women's Hospital
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Girish N Nadkarni
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Release 1.2