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KM

Kia Manoochehri

Regeneron (United States) US

36
Publications
3,981
Citations
19
H-Index
28
i10-Index
20.5
2yr Mean Cite
-
Cite/Paper
Data combined from OpenAlex + Semantic Scholar. OA = OpenAlex S2 = Semantic Scholar
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Publication & Citation Trends

Publications

0 total

Rare coding variants in CHRNB3 associate with reduced daily cigarette smoking across ancestries

Veera M. Rajagopal, A. Ziyatdinov, Tyler Joseph, Ariane Ayer, Mohsin Ahmed - Nature Communications, 2026
Cited by 0 Semantic Scholar

Population-scale repeat expansions elucidate disease risk and brain atrophy

Vijay Kumar Pounraja, J. Sul, Joseph Herman, S. O’Keeffe, Veera M. Rajagopal - Nature, 2026
Cited by 0 Semantic Scholar

Genomic Ascertainment of CHEK2-Related Cancer Predisposition

Sun Young Kim, Jung Kim, Mark F Ramos, J. Haley, D. Smelser - JAMA Network Open, 2025
Cited by 1 Semantic Scholar

Insights from the Biorepository and Integrative Genomics pediatric resource

S. Buonaiuto, F. Marsico, A. Mohammed, Lokesh K. Chinthala, Ernestine K. Amos-Abanyie - Nature Communications, 2025
Cited by 2 Semantic Scholar

The impact of common and rare genetic variants on bradyarrhythmia development OA

L. Weng, Joel T. Rämö, S. Jurgens, S. Khurshid, M. Chaffin - Nature Genetics, 2025
Cited by 10 Semantic Scholar

Thrombotic risk determined by ABO, F8, and VWF variants in a population-based cohort study

Eric Manderstedt, C. Halldén, C. Lind-Halldén, J. Elf, Peter J Svensson - Research and Practice in Thrombosis and Haemostasis, 2025
Cited by 2 Semantic Scholar

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

Seung Hoan Choi, S. Jurgens, Ling Xiao, M. Hill, Christopher M. Haggerty - Nature Genetics, 2025
Cited by 18 Semantic Scholar

Risk of lymphoid malignancy associated with cancer predisposition genes

N. Boddicker, R. Mwangi, Dennis P Robinson, C. Allmer, A. Rosenthal - Blood Cancer Journal, 2025
Cited by 5 Semantic Scholar

Exclusion-based exome sequencing in critically ill adults 18–40 years old has a 24% diagnostic rate and finds racial disparities in access to genetic testing

Jessica I Gold, Colleen M. Kripke, A. Mansfield, Alexander Li, Alexander Lopez - American Journal of Human Genetics, 2025
Cited by 2 Semantic Scholar

Author Correction: A deep catalogue of protein-coding variation in 983,578 individuals OA

Kathie Y. Sun, X. Bai, Siying Chen, Suying Bao, Chuanyi Zhang - Nature, 2025
Cited by 0 Semantic Scholar

Research Topics

Genetic Associations and Epidemiology (12) Genomics and Rare Diseases (8) BRCA gene mutations in cancer (6) Blood Coagulation and Thrombosis Mechanisms (4) Cardiomyopathy and Myosin Studies (3)

Affiliations

German Cancer Research Center
DE 2020 - 2020
Regeneron (United States)
US 2026 - 2020
Heidelberg University
DE 2020 - 2020
Geisinger Health System
US 2025 - 2025

External Profiles

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