Martina Brueckner

Yale University US

0000-0003-0347-5389

120

Publications

10,908

Citations

H-Index

i10-Index

4.71

2yr Mean Cite

Cite/Paper

Data combined from OpenAlex + Semantic Scholar. OA = OpenAlex S2 = Semantic Scholar

Verify on Google Scholar

Publication & Citation Trends

Publications

0 total

P204: Evaluating the clinical validity of gene-disease relationships in congenital heart disease OA

A. Roberts, S. Morton, Shannon Nees, Kezang Tshering, Julie Ratliff - Genetics in Medicine Open, 2026

Cited by 0 Semantic Scholar

Machine learning to infer neurocognitive testing scores among adolescents and young adults with congenital heart disease OA

Mohammad Arafat Hussain, Sheng He, H. R. Adams, Evdokia Anagnoustou, David C. Bellinger - Communications Medicine, 2026

Cited by 1 Semantic Scholar

Uniparental Disomy Reveals Hidden Genetic Causes of Congenital Heart Disease OA

Nahyun Kong, Javier Abello, Christopher J. Yoon, Andrew Ruttenberg, Zefan Li - Research Square, 2026

Cited by 0 Semantic Scholar

Recessive genetic contribution to congenital heart disease in 5,424 probands OA

W. Dong, Sheng-Chih Jin, M. Sierant, Ziyu Lu, Boyang Li - Proceedings of the National Academy of Sciences of the United States of America, 2025

Cited by 12 Semantic Scholar

Modeling SMAD2 Mutations in Induced Pluripotent Stem Cells Provides Insights Into Cardiovascular Disease Pathogenesis OA

T. Ward, Sarah U. Morton, Gabriela Venturini, Warren Tai, Min-Young Jang - Journal of the American Heart Association : Cardiovascular and Cerebrovascular Disease, 2025

Cited by 1 Semantic Scholar

Genome sequencing is critical for forecasting outcomes following congenital cardiac surgery OA

W. S. Watkins, E. J. Hernandez, T. Miller, N. Blue, R. Zimmerman - Nature Communications, 2025

Cited by 3 Semantic Scholar

Abstract 4359742: Thrombophilia Variants Do Not Predict Thrombotic Events in Congenital Heart Disease: Insights from the Pediatric Cardiac Genomics Consortium

Feria A. Ladha, Christina VanderPluym, Paul Avillach, M. Brueckner, Wendy Chung - Circulation, 2025

Cited by 0 Semantic Scholar

Enrichment of tandem repeat element variants near CHD genes identified by short- and long-read genome sequencing OA

Abhilash Suresh, Sarah U. Morton, D. Quiat, S. DePalma, J. Gorham - BMC Medical Genomics, 2025

Cited by 1 Semantic Scholar

Noncoding variants and sulcal patterns in congenital heart disease: Machine learning to predict functional impact OA

Enrique Mondragon-Estrada, Jane W. Newburger, S. DePalma, M. Brueckner, John Cleveland - iScience, 2024

Cited by 3 Semantic Scholar

Research Topics

Congenital heart defects research (75) Congenital Heart Disease Studies (46) Genomics and Rare Diseases (28) Genetic and Kidney Cyst Diseases (24) Developmental Biology and Gene Regulation (14)