Kathleen A. Leppig

Also affiliated with University of Washington Medical Center

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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 15 papers. Top paper: “Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study”.

Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study

Circulation(2021)10.1161/circulationaha.121.055562

N/A

1.2DataRank · unranked

49 citations

Giovanni Davogustto, Christian M. Shaffer, Carlos G. Vanoye, Reshma R. Desai, Eric Farber‐Eger +46 more

Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updates

Genetics in Medicine(2021)10.1016/j.gim.2021.10.010

N/A

0.494DataRank · unranked

26 citations

Wanfeng Yu, Andrea M. Oza, Megan Hawley, Prathik K. Vijay Kumar, Christopher Koch +12 more

Developmental epileptic encephalopathy in DLG4‐related synaptopathy

Epilepsia(2023)10.1111/epi.17876

N/A

0.434DataRank · unranked

17 citations

Amanda M. Levy, Elena Gardella, Ángel Aledo‐Serrano, Amitha Ananth, Alejandro Brea‐Fernández +59 more

Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome

Annals of Clinical and Translational Neurology(2023)10.1002/acn3.51786

N/A

0.241DataRank · unranked

4 citations

Ghayda Mirzaa, Elizabeth Blue, Giuseppe Albano, Danny E. Miller, Aimee Allworth +28 more

Dual diagnosis of UQCRFS1-related mitochondrial complex III deficiency and recessive GJA8-related cataracts

Rare(2024)10.1016/j.rare.2024.100040

N/A

0.208DataRank · unranked

3 citations

Samuel J. Huang, Alyna Khan, Katie Golden‐Grant, Brenna Boyd, Elisabeth A. Rosenthal +37 more

Synchronized long-read genome, methylome, epigenome, and transcriptome for resolving a Mendelian condition

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.09.26.559521

N/A

0DataRank · unranked

7 citations

Jonas Korlach, Kiara C. Eldred, Elliott Swanson, Jason G. Underwood, Yong-Han Hank Cheng +31 more

Genetic Predictors of Blood Pressure Traits are Associated with Preeclampsia

medRxiv(2023)10.1101/2023.02.09.23285734

N/A

0DataRank · unranked

0 citations

Jacklyn N. Hellwege, Joseph H. Breeyear, Brenda Xiao, Gail P. Jarvik, Ian B. Stanaway +10 more

Genetic predictors of blood pressure traits are associated with preeclampsia

Scientific Reports(2024)10.1038/s41598-024-68469-6

N/A

0DataRank · unranked

2 citations

Jacklyn N. Hellwege, Joseph H. Breeyear, Brenda Xiao, Gail P. Jarvik, Ian B. Stanaway +10 more

Synchronized long-read genome, methylome, epigenome and transcriptome profiling resolve a Mendelian condition

Nature Genetics(2025)10.1038/s41588-024-02067-0

N/A

0DataRank · unranked

34 citations

Jonas Korlach, Kiara C. Eldred, Elliott Swanson, Jason G. Underwood, Stephanie C. Bohaczuk +33 more

De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy

Genetics in Medicine(2020)10.1038/s41436-020-01020-w

N/A

0DataRank · unranked

47 citations

Heinrich Sticht, Pia Zacher, Bernt Popp, Holly E. Babcock, Dewi P. Bakker +53 more

Implementation of a Traceback Testing Program for Ovarian Cancer: Findings from the FACTS Study

Cancers(2025)10.3390/cancers17071154

N/A

0DataRank · unranked

2 citations

M. Cabell Jonas, Paula R. Blasi, Adam H. Buchanan, Pim Suwannarat, Kathleen A. Leppig +25 more

Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations

UNC Libraries(2020)10.17615/nh7z-zg10

N/A

0DataRank · unranked

1 citations

Kathryn F. Peters, Lewis B. Holmes, David J. Aughton, Laura Mazzanti, Kathleen A. Leppig +27 more

Patient and Family Preferences on Health System-Led Direct Contact for Cascade Screening

Journal of Personalized Medicine(2021)10.3390/jpm11060538

N/A

0DataRank · unranked

46 citations

Paula R. Blasi, Marlaine Figueroa Gray, Brooks Tiffany, Aaron Scrol, James D. Ralston +5 more

What improves the likelihood of people receiving genetic test results communicating to their families about genetic risk?

Patient Education and Counseling(2021)10.1016/j.pec.2021.01.001

N/A

0DataRank · unranked

15 citations

Sukh Makhnoon, Brian H. Shirts, Stephanie M. Fullerton, Eric B. Larson, James D. Ralston +5 more

Feasibility and Assessment of a Cascade Traceback Screening Program (FACTS): Protocol for a Multisite Study to Implement and Assess an Ovarian Cancer Traceback Cascade Testing Program

Journal of Personalized Medicine(2021)10.3390/jpm11060543

N/A

0DataRank · unranked

6 citations

Nora B. Henrikson, M. Cabell Jonas, Sundeep Basra, Paula R. Blasi, Jennifer Valeska Elli Brown +21 more