Chloe Reuter

Also affiliated with Stanford Medicine, Center for Inherited Blood Disorders, Stanford University

Biochemistry, Genetics and Molecular BiologyMedicine

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 3%percentile

0.931Author DataRank

Indexed papers

2in 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 2 indexed papers 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel: Reappraisal of Genes associated with Hypertrophic Cardiomyopathy

medRxiv(2024)10.1101/2024.07.29.24311195

Top 40%

0.470DataRank

Top 40%11 citations

Amber Waddell, Babken Asatryan, Emma Owens, Courtney L Thaxton, Mhy-Lanie Adduru +25 more

Papers

Driven by 23 papers — median percentile 59. Top paper: “Beyond the exome: What’s next in diagnostic testing for Mendelian conditions”.

Beyond the exome: What’s next in diagnostic testing for Mendelian conditions

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.009

N/A

2.2DataRank · unranked

123 citations

Chloe Reuter, Shruti Marwaha, Medhat Mahmoud, Michael Duyzend, Hayk Barseghyan +91 more

ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel: Reappraisal of Genes associated with Hypertrophic Cardiomyopathy

medRxiv(2024)10.1101/2024.07.29.24311195

Top 40%

0.470DataRank

Top 40%11 citations

Amber Waddell, Babken Asatryan, Emma Owens, Courtney L Thaxton, Mhy-Lanie Adduru +25 more

Population-scale variability at short tandem repeat loci reveals pathogenicity signature

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.01.06.631535

Top 41%

0.461DataRank

Top 41%11 citations

Isaac Xu, Sarah Fazal, Egor Dolzhenko, David Pellerin, Ben Weisburd +30 more

Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease

Genome Research(2025)10.1101/gr.279323.124

N/A

0.425DataRank · unranked

11 citations

Bohan Ni, Chloe Reuter, John E. Gorzynski, Sarah Fazal, Devon Bonner +13 more

The current landscape of clinical exome and genome reanalysis in the U.S.

Journal of Genetic Counseling(2025)10.1002/jgc4.1968

N/A

0.208DataRank · unranked

3 citations

Jennefer N. Carter, Matthew T. Wheeler, Chloe Reuter, Michelle Frees

Emery–Dreifuss muscular dystrophy Type 1 is associated with a high risk of malignant ventricular arrhythmias and end-stage heart failure

European Heart Journal(2023)10.1093/eurheartj/ehad561

N/A

0DataRank · unranked

20 citations

Petros Syrris, Alexandros Protonotarios, Athanasios Bakalakos, Jean-François Pruny, Raffaello Ditaranto +27 more

Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest

Circulation Genomic and Precision Medicine(2023)10.1161/circgen.122.003792

N/A

0DataRank · unranked

14 citations

Jochen Weile, Prince J. Kannankeril, Andrew M. Glazer, Chloe Reuter, Calum A. MacRae +5 more

Arrhythmias including atrial fibrillation and congenital heart disease in Kleefstra syndrome: a possible epigenetic link

EP Europace(2023)10.1093/europace/euae003

N/A

0DataRank · unranked

7 citations

Tanja Zdolšek Draksler, Arianne Bouman, Joost Kummeling, Matthew T. Wheeler, Chloe Reuter +9 more

Beyond the exome: what's next in diagnostic testing for Mendelian conditions

arXiv (Cornell University)(2023)10.48550/arxiv.2301.07363

N/A

0DataRank · unranked

5 citations

Chloe Reuter, Shruti Marwaha, Medhat Mahmoud, Michael Duyzend, Hayk Barseghyan +19 more

P643: Transcriptome sequencing increases yield of Mendelian disease diagnosis

Genetics in Medicine Open(2023)10.1016/j.gimo.2023.100708

N/A

0DataRank · unranked

0 citations

Rachel Ungar, Pagé C. Goddard, Jennefer N. Kohler, Chloe Reuter, Shruti Marwaha +4 more

Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

Genetics in Medicine(2024)10.1016/j.gim.2024.101166

N/A

0DataRank · unranked

11 citations

Nicole Legro, Dustin Baldridge, Jimann Shin, Angela Bowman, Berrak Uğur +89 more

Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

Genetics in Medicine(2024)10.1016/j.gim.2024.101115

N/A

0DataRank · unranked

6 citations

Lauren C. Briere, Chloe Reuter, Perman Gochyyev, Maria T. Acosta, David R. Adams +94 more

Assessing and attending to psychosocial concerns in genetic counseling: Proposing the BATHE method

Journal of Genetic Counseling(2024)10.1002/jgc4.1998

N/A

0DataRank · unranked

3 citations

Emily Higgs, Elizabeth Pollard, Mattie Monroe, Thuy‐Mi P. Nguyen, MaryAnn Campion +2 more

De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders

medRxiv(2024)10.1101/2024.04.07.24305438

N/A

0DataRank · unranked

10 citations

Ruebena Dawes, Hyung Chul Kim, Sarah L. Stenton, Susan Walker, Alicia Ljungdahl +92 more

Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease

medRxiv(2024)10.1101/2024.03.22.24304565

N/A

0DataRank · unranked

5 citations

Bohan Ni, Chloe Reuter, John E. Gorzynski, Sarah Fazal, Devon Bonner +13 more

Genes Associated With Hypertrophic Cardiomyopathy

Journal of the American College of Cardiology(2025)10.1016/j.jacc.2024.12.010

N/A

0DataRank · unranked

52 citations

Amber Waddell, Babken Asatryan, Emma Owens, Courtney L Thaxton, Mhy-Lanie Adduru +25 more

An optimized variant prioritization process for rare disease diagnostics: recommendations for Exomiser and Genomiser

Genome Medicine(2025)10.1186/s13073-025-01546-1

N/A

0DataRank · unranked

8 citations

Shruti Marwaha, Alistair Ward, Shilpa N. Kobren, Jennefer N. Carter, Undiagnosed Diseases Network +94 more

Researcher views on returning results from multi-omics data to research participants: insights from The Molecular Transducers of Physical Activity Consortium (MoTrPAC) Study

BMC Medical Ethics(2025)10.1186/s12910-025-01174-9

N/A

0DataRank · unranked

3 citations

Caroline Stanclift, Chloe Reuter, Jennefer N. Carter, Kathleen Murphy, Maléne E. Lindholm +2 more

Biallelic variants in the non-coding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes

medRxiv(2025)10.1101/2025.08.13.25333306

N/A

0DataRank · unranked

5 citations

Alexander J. M. Blakes, Yuyang Chen, Joachim De Jonghe, Javeria Raza Alvi, Florence Amblard +69 more

De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.02.016

N/A

0DataRank · unranked

70 citations

Chloe Reuter, Maura Ruzhnikov, Anita E. Beck, Emily Farrow, Lisa Emrick +91 more

Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science

Genetics in Medicine(2020)10.1038/s41436-020-00984-z

N/A

0DataRank · unranked

42 citations

Cecilia Esteves, Anna Bican, Rebecca C. Spillmann, Heidi Cope, Allyn McConkie‐Rosell +89 more

The genetic architecture of Plakophilin 2 cardiomyopathy

Genetics in Medicine(2021)10.1038/s41436-021-01233-7

N/A

0DataRank · unranked

36 citations

Anna Kirillova, Chloe Reuter, John Garcia, Hana Zouk, Megan Hawley +28 more

A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network

Genetics in Medicine(2022)10.1016/j.gim.2022.12.001

N/A

0DataRank · unranked

1 citations

Queenie K.‐G. Tan, Chloe Reuter, Kelly Schoch, Jennefer N. Kohler, Devon Bonner +94 more

Chloe Reuter

Indexed papers

Top data-sharing exemplar

Papers