Noura S. Abul‐Husn

ORCID: 0000-0002-5179-1944

Also affiliated with Genomic Health (United States), Icahn School of Medicine at Mount Sinai

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 37 papers. Top paper: “Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations”.

Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

Nature Medicine(2024)10.1038/s41591-024-02796-z

N/A

4.8DataRank · unranked

196 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Joshua Arias, Gillian M. Belbin +73 more

Returning integrated genomic risk and clinical recommendations: The eMERGE study

Genetics in Medicine(2023)10.1016/j.gim.2023.100006

N/A

2.6DataRank · unranked

121 citations

Aimee Allworth, Harris T. Bland, Pedro J. Caraballo, Rex L. Chisholm, Ellen Wright Clayton +95 more

ACMG 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)

Genetics in Medicine(2023)10.1016/j.gim.2023.100866

N/A

0.911DataRank · unranked

433 citations

Kristy Lee, Noura S. Abul‐Husn, Laura M. Amendola, Kyle B. Brothers, Wendy K. Chung +9 more

Genome-wide polygenic score to predict chronic kidney disease across ancestries

Nature Medicine(2022)10.1038/s41591-022-01869-1

N/A

0.764DataRank · unranked

162 citations

Michael C. Turchin, Amit Patki, Vinodh Srinivasasainagendra, Ning Shang, Rajiv Nadukuru +34 more

Toward a fine-scale population health monitoring system

Cell(2021)10.1016/j.cell.2021.03.034

N/A

0.763DataRank · unranked

161 citations

Sinéad Cullina, Stéphane Wenric, Emily R. Soper, Benjamin Scott Glicksberg, Denis Torre +18 more

Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations

medRxiv(2023)10.1101/2023.05.25.23290535

N/A

0.330DataRank · unranked

8 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Josh Arias, Gillian M. Belbin +71 more

Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients

medRxiv(2023)10.1101/2023.03.18.23286992

N/A

0.312DataRank · unranked

7 citations

Priya Marathe, Nicole Kelly, Katherine E. Bonini, Monisha Sebastin, Jacqueline A. Odgis +22 more

Admixture mapping of peripheral artery disease in a Dominican population reveals a putative risk locus on 2q35

Frontiers in Genetics(2023)10.3389/fgene.2023.1181167

N/A

0.292DataRank · unranked

6 citations

Genevieve L. Wojcik, Ruhollah Shemirani, Derek Klarin, Bryan R. Gorman, Elena P. Sorokin +9 more

Genome-wide polygenic score with APOL1 risk genotypes predicts chronic kidney disease across major continental ancestries

medRxiv(2021)10.1101/2021.10.25.21265398

N/A

0.218DataRank · unranked

2 citations

Michael C. Turchin, Amit Patki, Vinodh Srinivasasainagendra, Ning Shang, Rajiv Nadukuru +33 more

Physician and informal care use explained by the Pediatric Quality of Life Inventory (PedsQL) in children with suspected genetic disorders

Quality of Life Research(2024)10.1007/s11136-024-03677-1

N/A

0.104DataRank · unranked

1 citations

Nicole Kelly, Ashley Fisher, Samuel F. Hohmann, Noura S. Abul‐Husn, John M. Greally +6 more

Detection of mosaic variants using genome sequencing in a large pediatric cohort

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.63062

N/A

0DataRank · unranked

14 citations

Katie M. Gallagher, Atteeq U. Rehman, Priya Marathe, Katherine E. Bonini, Monisha Sebastin +21 more

Diverse and unselected adults with clinically relevant ACADS variants lack evidence of metabolic disease

Molecular Genetics and Metabolism(2022)10.1016/j.ymgme.2022.106971

N/A

0DataRank · unranked

8 citations

Eimear E. Kenny, Noura S. Abul‐Husn, Margo Sheck Breilyn

Prescriber Adoption of SLCO1B1Genotype‐Guided Simvastatin Clinical Decision Support in a Clinical Pharmacogenetics Program

Clinical Pharmacology & Therapeutics(2022)10.1002/cpt.2773

N/A

0DataRank · unranked

6 citations

Stuart A. Scott, Tom Kaszemacher, Stephen B. Ellis, Ana Mejia, Alanna Gomez +8 more

Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients

Genetics in Medicine(2023)10.1016/j.gim.2023.100880

N/A

0DataRank · unranked

42 citations

Priya N. Marathe, Nicole R. Kelly, Katherine E. Bonini, Monisha Sebastin, Jacqueline A. Odgis +22 more

Association of HSD17B13 and PNPLA3 With Liver Enzymes and Fibrosis in Hispanic/Latino Individuals of Diverse Genetic Ancestries

Clinical Gastroenterology and Hepatology(2023)10.1016/j.cgh.2022.12.025

N/A

0DataRank · unranked

20 citations

Emily R. Soper, Ning Ma, Vikas Pejaver, Scott L. Friedman, Andrea D. Branch +4 more

Specifications of the ACMG/AMP Variant Classification Guidelines for Germline DICER1 Variant Curation

Human Mutation(2023)10.1155/2023/9537832

N/A

0DataRank · unranked

15 citations

Megan N. Frone, Hannah C. Cox, Stephanie B. Crowley, Susan Hiraki, Noriko N. Yokoyama +20 more

Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program

Clinical Genetics(2023)10.1111/cge.14365

N/A

0DataRank · unranked

6 citations

Amanda Thomas‐Wilson, Priya N. Marathe, Monisha Sebastin, Jacqueline A. Odgis, Miranda Di Biase +24 more

The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic results disclosure in diverse families

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.10.016

N/A

0DataRank · unranked

6 citations

Nicole Kelly, Jacqueline A. Odgis, Katie M. Gallagher, Monisha Sebastin, Katherine E. Bonini +18 more

Admixture Mapping of Peripheral Artery Disease in a Dominican Population Reveals a Novel Risk Locus on 2q35

medRxiv(2023)10.1101/2023.03.27.23287788

N/A

0DataRank · unranked

0 citations

Genevieve L. Wojcik, Ruhollah Shemirani, Derek Klarin, Bryan R. Gorman, Elena P. Sorokin +9 more

The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic counseling in racially and ethnically diverse families

medRxiv(2023)10.1101/2023.07.05.23292193

N/A

0DataRank · unranked

0 citations

Nicole Kelly, Jacqueline A. Odgis, Katie M. Gallagher, Monisha Sebastin, Katherine E. Bonini +18 more

Physician services and costs after disclosure of diagnostic sequencing results in the NYCKidSeq program

Genetics in Medicine(2023)10.1016/j.gim.2023.101011

N/A

0DataRank · unranked

0 citations

Nicole Kelly, Ashley Fisher, Samuel F. Hohmann, Monisha Sebastin, Miranda Di Biase +14 more

Evolving knowledge of red flag clinical features associated with TTR p.(Val142Ile) in a diverse electronic health-record-linked biobank

Genetics in Medicine(2024)10.1016/j.gim.2024.101346

N/A

0DataRank · unranked

7 citations

Connor B Benson, Alexandra McClellan, Gillian M. Belbin, Eimear E. Kenny, Noura S. Abul‐Husn +1 more

Consideration of disease penetrance in the selection of secondary findings gene-disease pairs: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2024)10.1016/j.gim.2024.101142

N/A

0DataRank · unranked

13 citations

Kristy Lee, Noura S. Abul‐Husn, Laura M. Amendola, Kyle B. Brothers, Wendy K. Chung +8 more

Employing effective recruitment and retention strategies to engage a diverse pediatric population in genomics research

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.10.015

N/A

0DataRank · unranked

4 citations

Katherine E. Bonini, Laura Scarimbolo, Nicole Kelly, Beverly J. Insel, Sabrina A. Suckiel +36 more

Evaluating parental personal utility of pediatric genetic and genomic testing in a diverse, multilingual population

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100321

N/A

0DataRank · unranked

1 citations

Sabrina A. Suckiel, Katherine E. Bonini, Nicole Kelly, Laura Scarimbolo, Beverly J. Insel +22 more

ACMG SF v3.3 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)

Genetics in Medicine(2025)10.1016/j.gim.2025.101454

N/A

0DataRank · unranked

56 citations

Noura S. Abul‐Husn, Laura M. Amendola, Kyle B. Brothers, Wendy K. Chung, Michael H. Gollob +11 more

A common variant in PNPLA3 is associated with age at diagnosis of NAFLD in patients from a multi-ethnic biobank

Journal of Hepatology(2020)10.1016/j.jhep.2020.01.029

N/A

0DataRank · unranked

62 citations

Gillian M. Belbin, Elena P. Sorokin, Tielman Van Vleck, Genevieve L. Wojcik, Arden Moscati +7 more

Patient and providers’ perspectives on using the GUÍA digital tool to enhance genomic results disclosure

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103451

N/A

0DataRank · unranked

1 citations

Sabrina A. Suckiel, Laura Golfinopoulos, Nicole R. Kelly, Katherine E. Bonini, Priya N. Marathe +15 more

The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children

medRxiv(2020)10.1101/2020.09.02.20186361

N/A

0DataRank · unranked

1 citations

Katie M. Gallagher, Sabrina A. Suckiel, Katherine E. Donohue, Michelle A. Ramos, Nicole Kelly +41 more

GUÍA: a digital platform to facilitate result disclosure in genetic counseling

medRxiv(2020)10.1101/2020.09.14.20194191

N/A

0DataRank · unranked

0 citations

Jaqueline A. Odgis, Katie M. Gallagher, Jessica Rodriguez, Dana Watnick, Gabrielle Bertier +27 more

GenomeDiver: A platform for phenotype-guided medical genomic diagnosis

medRxiv(2020)10.1101/2020.11.22.20236430

N/A

0DataRank · unranked

0 citations

Christian Stolte, Kevin Shi, Faygel Beren, Noura S. Abul‐Husn, Gabrielle Bertier +12 more

The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children

Research Square(2020)10.21203/rs.3.rs-64844/v1

N/A

0DataRank · unranked

0 citations

Katie M. Gallagher, Sabrina A. Suckiel, Katherine E. Donohue, Michelle A. Ramos, Nicole Kelly +41 more

Genetic identification of a common collagen disease in Puerto Ricans via identity-by-descent mapping in a health system

UNC Libraries(2020)10.17615/mv5t-7356

N/A

0DataRank · unranked

0 citations

Jacqueline A. Odgis, Peters, Ulrike, Ruth J. F. Loos, Eimear E. Kenny, Claudia Schurmann +27 more

GUÍA: a digital platform to facilitate result disclosure in genetic counseling

Genetics in Medicine(2021)10.1038/s41436-020-01063-z

N/A

0DataRank · unranked

28 citations

Jaqueline A. Odgis, Katie M. Gallagher, Jessica Rodriguez, Dana Watnick, Gabrielle Bertier +27 more

Leveraging health systems data to characterize a large effect variant conferring risk for liver disease in Puerto Ricans

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.09.016

N/A

0DataRank · unranked

14 citations

Stephanie Rutledge, Tetyana Dodatko, Sinéad Cullina, Michael C. Turchin, Sumita Kohli +7 more

Retinol Binding Protein 4 as a Screening Biomarker for Hereditary TTR Amyloidosis in African American Adults With TTR V142I

Journal of Cardiac Failure(2021)10.1016/j.cardfail.2021.05.009

N/A

0DataRank · unranked

7 citations

Noura S. Abul‐Husn, Amy Kontorovich

Left ventricular strain does not differentiate amyloidogenic profiles in at-risk individuals with TTR Val142Ile

medRxiv(2021)10.1101/2021.01.26.21250565

N/A

0DataRank · unranked

1 citations

Wenli Zhao, M. Gavalas, Helen Hashemi, Steve Liao, Eman Rashed +6 more