Christa Lese Martin

Autism & Developmental Medicine Institute

Also affiliated with Geisinger Health System

Biochemistry, Genetics and Molecular Biology

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 4%percentile

0.575Author 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.

The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources

medRxiv(2022)10.1101/2022.01.03.21268593

Top 34%

0.575DataRank

Top 34%17 citations

Scott Goehringer, Lawrence Babb, Fowzan S. Alkuraya, Joanna Amberger, Mutaz Amin +41 more

Papers

Driven by 29 papers — median percentile 33. Top paper: “ACMG SF v3.0 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)”.

ACMG SF v3.0 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(2021)10.1038/s41436-021-01172-3

N/A

13.5DataRank · unranked

563 citations

Kristy Lee, Wendy K. Chung, Allan Gordon, Gail E. Herman, Teri E. Klein +13 more

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2021)10.1038/s41436-021-01171-4

N/A

9.7DataRank · unranked

266 citations

Kristy Lee, Allan Gordon, Laura M. Amendola, Kathy Adelman, Sherri J. Bale +13 more

Correction to: ACMG SF v3.0 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(2021)10.1038/s41436-021-01278-8

N/A

1.6DataRank · unranked

29 citations

Kristy Lee, Wendy K. Chung, Allan Gordon, Gail E. Herman, Teri E. Klein +13 more

Modernizing the Data Infrastructure for Clinical Research to Meet Evolving Demands for Evidence

JAMA(2024)10.1001/jama.2024.0268

N/A

0.940DataRank · unranked

25 citations

Caroline Marra, Atul Janardhan Butte, Laura Esserman, Lee A. Fleisher, Cynthia I. Grossman +64 more

The Integration of Clinical Trials With the Practice of Medicine

JAMA(2024)10.1001/jama.2024.4088

N/A

0.609DataRank · unranked

57 citations

Alison J. Huang, Roger J. Lewis, Amy P. Abernethy, Robert M. Califf, Martin Landray +63 more

The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources

medRxiv(2022)10.1101/2022.01.03.21268593

Top 34%

0.575DataRank

Top 34%17 citations

Scott Goehringer, Lawrence Babb, Fowzan S. Alkuraya, Joanna Amberger, Mutaz Amin +41 more

Generating Clinical-Grade Gene–Disease Validity Classifications Through the ClinGen Data Platforms

Annual Review of Biomedical Data Science(2024)10.1146/annurev-biodatasci-102423-112456

N/A

0.502DataRank · unranked

16 citations

Courtney L Thaxton, Tristan H Nelson, Marina T. DiStefano, Juliann M. Savatt, Matthew Brush +25 more

All for one and one for all: heterogeneity of genetic etiologies in neurodevelopmental psychiatric disorders

Current Opinion in Genetics & Development(2021)10.1016/j.gde.2021.02.015

N/A

0DataRank · unranked

29 citations

Christa Lese Martin, Daniel Moreno‐De‐Luca

Recontacting registry participants with genetic updates through GenomeConnect, the ClinGen patient registry

Genetics in Medicine(2021)10.1038/s41436-021-01197-8

N/A

0DataRank · unranked

17 citations

Danielle R. Azzariti, David H. Ledbetter, Emily Palen, Heidi L. Rehm, Erin Rooney Riggs +2 more

Harnessing rare variants in neuropsychiatric and neurodevelopment disorders—a Keystone Symposia report

Annals of the New York Academy of Sciences(2021)10.1111/nyas.14658

N/A

0DataRank · unranked

7 citations

Ryan H. Purcell, Elise Robinson, Jacob Vorstman, Wendy K. Chung, John N. Constantino +9 more

Frequency of truncating FLCN variants and Birt-Hogg-Dubé–associated phenotypes in a health care system population

Genetics in Medicine(2022)10.1016/j.gim.2022.05.006

N/A

0DataRank · unranked

33 citations

Hermela Shimelis, Andrés Moreno-De-Luca, Natasha T. Strande, Matthew T. Oetjens, David H. Ledbetter +4 more

Clinical validity assessment of genes frequently tested on intellectual disability/autism sequencing panels

Genetics in Medicine(2022)10.1016/j.gim.2022.05.001

N/A

0DataRank · unranked

25 citations

Taylor I. Bingaman, Carrie-Ann Barry, Andrea Behlmann, Krista Bluske, Bret L. Bostwick +36 more

Phenotypic shift in copy number variants: Evidence in 16p11.2 duplication syndrome

Genetics in Medicine(2022)10.1016/j.gim.2022.09.011

N/A

0DataRank · unranked

10 citations

Brenda Finucane, Andrés Moreno-De-Luca, Lauren K. Walsh, Christa Lese Martin, David H. Ledbetter +1 more

Frequency of FLCN Loss of Function Variants and Birt-Hogg-Dubé-Associated Phenotypes in a Healthcare System Population

medRxiv(2022)10.1101/2022.01.31.22269926

N/A

0DataRank · unranked

0 citations

Hermela Shimelis, Andrés Moreno-De-Luca, Natasha T. Strande, Matthew T. Oetjens, David H. Ledbetter +4 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

0DataRank · unranked

425 citations

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

Systematic analysis of variants escaping nonsense-mediated decay uncovers candidate Mendelian diseases

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.11.007

N/A

0DataRank · unranked

37 citations

María J. Guillen Sacoto, Francisca Millan, Zhancheng Zhang, Stephen McGee, Matthew T. Oetjens +11 more

Toward robust clinical genome interpretation: Developing a consistent terminology to characterize Mendelian disease-gene relationships—allelic requirement, inheritance modes, and disease mechanisms

Genetics in Medicine(2023)10.1016/j.gim.2023.101029

N/A

0DataRank · unranked

17 citations

Marina T. DiStefano, Erin Rooney Riggs, Katherine Josephs, Fowzan S. Alkuraya, Joanna Amberger +21 more

Towards robust clinical genome interpretation: developing a consistent terminology to characterize disease-gene relationships - allelic requirement, inheritance modes and disease mechanisms

medRxiv(2023)10.1101/2023.03.30.23287948

N/A

0DataRank · unranked

7 citations

Marina T. DiStefano, Erin Rooney Riggs, Katherine Josephs, Fowzan S. Alkuraya, Joanna Amberger +21 more

A genome-first study of sex chromosome aneuploidies provides evidence of Y chromosome dosage effects on autism risk

Nature Communications(2024)10.1038/s41467-024-53211-7

N/A

0DataRank · unranked

15 citations

Brenda Finucane, Scott M. Myers, Lauren K. Walsh, John M. Seibert, Christa Lese Martin +3 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

Genetic modifiers and ascertainment drive variable expressivity of complex disorders

medRxiv(2024)10.1101/2024.08.27.24312158

N/A

0DataRank · unranked

5 citations

Corrine Smolen, Anastasia Tyryshkina, Lucilla Pizzo, Deepro Banerjee, Matthew T. Oetjens +65 more

Contributors

Genomic and Personalized Medicine(2013)10.1016/b978-0-12-382227-7.00124-5

N/A

0DataRank · unranked

0 citations

Minhaz Uddin Ahmed, Sun Hee Ahn, R. Rand Allingham, Jude Alsarraj, Matthew L. Anderson +228 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

Insufficient Evidence for “Autism-Specific” Genes

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.04.004

N/A

0DataRank · unranked

169 citations

Thomas D. Challman, Raphael Bernier, Thomas Bourgeron, Wendy K. Chung, John N. Constantino +8 more

Clinical outcomes of a genomic screening program for actionable genetic conditions

Genetics in Medicine(2020)10.1038/s41436-020-0876-4

N/A

0DataRank · unranked

154 citations

H. Lester Kirchner, M. Schwartz, Melissa Kelly, Tara Schmidlen, Laney K. Jones +15 more

A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation

UNC Libraries(2020)10.17615/0tee-nv95

N/A

0DataRank · unranked

1 citations

Christa Lese Martin, Evans, James P., Meredith Weaver, Katrina A.B. Goddard, Margaret Piper +19 more

Insufficient Evidence for “Autism-Specific” Genes

OSF Preprints (OSF Preprints)(2020)10.31219/osf.io/24gm3

N/A

0DataRank · unranked

3 citations

Thomas D. Challman, Raphael Bernier, Thomas Bourgeron, Wendy K. Chung, John N. Constantino +8 more

Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource

UNC Libraries(2020)10.17615/dtq0-px12

Top 100%

0DataRank

Top 100%0 citations

Ozge Ceyhan‐Birsoy, Bryce A. Seifert, Tam P. Sneddon, Natasha T. Strande, Erin M. Ramos +18 more

ClinGen — The Clinical Genome Resource

UNC Libraries(2020)10.17615/js2g-yk58

N/A

0DataRank · unranked

0 citations

Erin M. Ramos, David H. Ledbetter, Carlos D. Bustamante, Stephen T. Sherry, Michael S. Watson +9 more

Christa Lese Martin

Indexed papers

Top data-sharing exemplar

Papers