Valerie N. Morrill

National Institute of Neurological Disorders and Stroke

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

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 18 papers. Top paper: “Monogenic and Polygenic Contributions to QTc Prolongation in the Population”.

Monogenic and Polygenic Contributions to QTc Prolongation in the Population

Circulation(2022)10.1161/circulationaha.121.057261

N/A

1.7DataRank · unranked

50 citations

Valerie N. Morrill, Sean J. Jurgens, Seung Hoan Choi, Amelia W. Hall, Lu-Chen Weng +34 more

Adjusting for common variant polygenic scores improves yield in rare variant association analyses

Nature Genetics(2023)10.1038/s41588-023-01342-w

N/A

1.2DataRank · unranked

46 citations

James P. Pirruccello, Seung Hoan Choi, Valerie N. Morrill, Mark Chaffin, Steven A. Lubitz +3 more

Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank

Nature Genetics(2022)10.1038/s41588-021-01011-w

N/A

0.775DataRank · unranked

174 citations

Seung Hoan Choi, Valerie N. Morrill, Mark Chaffin, James P. Pirruccello, Jennifer L. Halford +65 more

Genetics of myocardial interstitial fibrosis in the human heart and association with disease

Nature Genetics(2023)10.1038/s41588-023-01371-5

N/A

0.670DataRank · unranked

86 citations

Paolo Di Achille, Marcus D. R. Klarqvist, Jonathan W. Cunningham, Matthew C. Hill, James P. Pirruccello +13 more

Rare and Common Genetic Variation Underlying the Risk of Hypertrophic Cardiomyopathy in a National Biobank

JAMA Cardiology(2022)10.1001/jamacardio.2022.1061

N/A

0.659DataRank · unranked

80 citations

Sean J. Jurgens, Dimitri Maamari, Liam Gaziano, Seung Hoan Choi, Valerie N. Morrill +6 more

Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk

Nature Genetics(2025)10.1038/s41588-025-02074-9

N/A

0.628DataRank · unranked

28 citations

Sean J. Jurgens, Ling Xiao, Matthew C. Hill, Christopher M. Haggerty, Garðar Sveinbjörnsson +95 more

The impact of common and rare genetic variants on bradyarrhythmia development

Nature Genetics(2025)10.1038/s41588-024-01978-2

N/A

0.464DataRank · unranked

21 citations

Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall +95 more

Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias

Circulation Genomic and Precision Medicine(2024)10.1161/circgen.123.004320

N/A

0.413DataRank · unranked

10 citations

Shaan Khurshid, Amelia Weber Hall, Victor Nauffal, Valerie N. Morrill, Yan V. Sun +54 more

Genetics of Myocardial Interstitial Fibrosis in the Human Heart and Association with Disease

medRxiv(2021)10.1101/2021.11.05.21265953

N/A

0.385DataRank · unranked

12 citations

Paolo Di Achille, Marcus D. R. Klarqvist, Jonathan W. Cunningham, James P. Pirruccello, Lu‐Chen Weng +12 more

Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes

Nature Communications(2022)10.1038/s41467-022-32009-5

N/A

0.360DataRank · unranked

10 citations

Valerie N. Morrill, Seung Hoan Choi, Sean J. Jurgens, Giorgio Melloni, Nicholas Marston +39 more

Monogenic and Polygenic Contributions to QTc Prolongation in the Population

medRxiv(2021)10.1101/2021.06.18.21258578

N/A

0.320DataRank · unranked

5 citations

Valerie N. Morrill, Sean J. Jurgens, Seung Hoan Choi, Amelia Weber Hall, Lu‐Chen Weng +33 more

Machine Learning to Understand Genetic and Clinical Factors Associated with the Pulse Waveform Dicrotic Notch

medRxiv(2021)10.1101/2021.12.09.21267484

N/A

0.241DataRank · unranked

4 citations

Paolo Di Achille, Valerie N. Morrill, Lu‐Chen Weng, Seung Hoan Choi, Shaan Khurshid +9 more

Genetic liability for gastrointestinal inflammation disorders and association with gastrointestinal symptoms in children with and without autism

American Journal of Medical Genetics Part B Neuropsychiatric Genetics(2023)10.1002/ajmg.b.32952

N/A

0.104DataRank · unranked

1 citations

Kelly S. Benke, John T. Brinton, Gnakub N. Soke, Laura A. Schieve, Victoria L. Fields +7 more

Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis

UNC Libraries(2024)10.17615/c1sy-3719

N/A

0DataRank · unranked

0 citations

Brandon K. Fornwalt, Chrissy Austin-Tse, Mark Chaffin, B.E. Cade, J Lee +43 more

Commonly used genomic arrays may lose information due to imperfect coverage of discovered variants for autism spectrum disorder

Journal of Neurodevelopmental Disorders(2024)10.1186/s11689-024-09571-8

N/A

0DataRank · unranked

1 citations

Jason Daniels, Luke P. Grosvenor, Valerie N. Morrill, Jason I. Feinberg, Kelly M. Bakulski +13 more

An epigenome-wide association study in the case-control study to explore early development identifies differential DNA methylation near ZFP57 as associated with autistic traits

Journal of Neurodevelopmental Disorders(2025)10.1186/s11689-025-09637-1

N/A

0DataRank · unranked

4 citations

Valerie N. Morrill, Rose Schrott, Jason Daniels, Ashley Song, Kelly S. Benke +11 more

The association of late-life depressive symptoms with brain amyloid-β deposition: the ARIC-PET study

Aging Brain(2025)10.1016/j.nbas.2025.100152

N/A

0DataRank · unranked

0 citations

Valerie N. Morrill, Marco T. Egle, Keenan A. Walker, Dean F. Wong, Rebecca F. Gottesman +1 more

Common and Rare Variant Contributions to Bradyarrhythmias from Multi-Ancestry Meta-Analyses

medRxiv(2023)10.1101/2023.09.24.23295485

N/A

0DataRank · unranked

0 citations

Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall +56 more