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KT

Katherine Tashman

Massachusetts Eye and Ear Infirmary US

ORCID 0000-0002-8938-1983
24
Publications
14,083
Citations
15
H-Index
16
i10-Index
0.5
2yr Mean Cite
-
Cite/Paper
Data combined from OpenAlex + Semantic Scholar. OA = OpenAlex S2 = Semantic Scholar
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Publication & Citation Trends

Publications

24 total

Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases PDF

E. Weeks, Jacob C. Ulirsch, Nathan Cheng, Brian L. Trippe, Rebecca S. Fine et al. - Nature Genetics, 2023
Cited by 287 OpenAlex

The relationship between safety‐net hospital status and outcomes among elderly head and neck cancer patients

K. Tashman, Elizabeth A Noyes, Chloe B Warinner, Joseph Ogbonna, E. Gomez - Head and Neck, 2023
Cited by 3 Semantic Scholar

Disruptions in maternal health service use during the COVID-19 pandemic in 2020: experiences from 37 health facilities in low-income and middle-income countries PDF

Zeus Aranda, Thierry Bindé, Katherine Tashman, A Tadikonda, Bill Mawindo et al. - BMJ Global Health, 2022
Cited by 231 OpenAlex

Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans PDF

Konrad J. Karczewski, Laurent C. Francioli, Grace Tiao, Beryl B. Cummings, Jessica Alföldi et al. - Nature, 2021
Cited by 97 OpenAlex

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals. OA

Joshua E. Motelow, G. Povysil, R. Dhindsa, Kate E Stanley, A. Allen - American Journal of Human Genetics, 2021
Cited by 2 Semantic Scholar

Significance testing for small annotations in stratified LD-Score regression OA

K. Tashman, R. Cui, L. O'Connor, B. Neale, H. Finucane - medRxiv, 2021
Cited by 23 Semantic Scholar

Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans OA

Sanna Gudmundsson, K. Karczewski, L. Francioli, G. Tiao, Beryl B. Cummings - Nature, 2021
Cited by 47 Semantic Scholar

The mutational constraint spectrum quantified from variation in 141,456 humans PDF

Konrad J. Karczewski, Laurent C. Francioli, Grace Tiao, Beryl B. Cummings, Jessica Alföldi et al. - Nature, 2020
Cited by 9,917 OpenAlex

Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases PDF

E. Weeks, Jacob C. Ulirsch, Nathan Cheng, Brian L. Trippe, Rebecca S. Fine et al. - medRxiv, 2020
Cited by 132 OpenAlex

A data harmonization pipeline to leverage external controls and boost power in GWAS OA

Danfeng Chen, K. Tashman, D. Palmer, B. Neale, K. Roeder - bioRxiv, 2020
Cited by 9 Semantic Scholar

Research Topics

Genomics and Rare Diseases (12) Genetics and Neurodevelopmental Disorders (7) Genetic Associations and Epidemiology (6) Epilepsy research and treatment (3) Bioinformatics and Genomic Networks (3)

Affiliations

Broad Institute
US 2023 - 2019
Massachusetts Eye and Ear Infirmary
US 2025 - 2023
Harvard University
US 2025 - 2022
Harvard University Press
US 2020 - 2020
Stanley Foundation
US 2021 - 2021

External Profiles

OpenAlex Profile Semantic Scholar Profile ORCID Profile Google Scholar

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