Martina Brueckner

Also affiliated with Pediatrics and Genetics

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 21 papers. Top paper: “Systems Analysis Implicates WAVE2 Complex in the Pathogenesis of Developmental Left-Sided Obstructive Heart Defects”.

Systems Analysis Implicates WAVE2 Complex in the Pathogenesis of Developmental Left-Sided Obstructive Heart Defects

JACC Basic to Translational Science(2020)10.1016/j.jacbts.2020.01.012

N/A

1.1DataRank · unranked

28 citations

Andrew D. Rouillard, Nicolas Fernandez, Zichen Wang, Alexander Lachmann, Sunita S. Shankaran +21 more

Genomic analyses implicate noncoding de novo variants in congenital heart disease

Nature Genetics(2020)10.1038/s41588-020-0652-z

N/A

0.779DataRank · unranked

179 citations

Sarah U. Morton, Seong Won Kim, Alexander Kitaygorodsky, Lauren K. Wasson, Kathleen Chen +30 more

De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.02.007

N/A

0.373DataRank · unranked

11 citations

Alice M. Tao, Shenzhao Lu, Mengqi Ma, Shabab B. Hannan, Rachel Slaugh +43 more

Association of genetic and sulcal traits with executive function in congenital heart disease

Annals of Clinical and Translational Neurology(2023)10.1002/acn3.51950

N/A

0.312DataRank · unranked

7 citations

Jane W. Newburger, David Wypij, Nina H. Thomas, Evdokia Anagnoustou, Martina Brueckner +17 more

Integrative modeling of transmitted and de novo variants identifies novel risk genes for congenital heart disease

Quantitative Biology(2021)10.15302/j-qb-021-0248

N/A

0.269DataRank · unranked

5 citations

Xue Zeng, Chentian Jin, Sheng Chih Jin, Weilai Dong, Martina Brueckner +4 more

Quantifying concordant genetic effects of de novo mutations on multiple disorders

eLife(2022)10.7554/elife.75551

N/A

0.269DataRank · unranked

5 citations

Lin Hou, Yu Shi, Sheng Chih Jin, Xue Zeng, Boyang Li +5 more

Genome sequencing is critical for forecasting outcomes following congenital cardiac surgery

Nature Communications(2025)10.1038/s41467-025-61625-0

N/A

0.241DataRank · unranked

4 citations

Edgar J. Hernández, Thomas A. Miller, Nathan R. Blue, Raquel M. Zimmerman, Eric R. Griffiths +21 more

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

iScience(2024)10.1016/j.isci.2024.111707

N/A

0.165DataRank · unranked

2 citations

Jane W. Newburger, Steven R. DePalma, Martina Brueckner, John D. Cleveland, Wendy K. Chung +16 more

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

BMC Medical Genomics(2025)10.1186/s12920-025-02191-8

N/A

0.165DataRank · unranked

2 citations

Sarah U. Morton, Daniel Quiat, Steven R. DePalma, Joshua M. Gorham, Martina Brueckner +5 more

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

Communications Medicine(2026)10.1038/s43856-026-01417-9

N/A

0.109DataRank · unranked

1 citations

Sheng He, Heather R. Adams, Evdokia Anagnoustou, David C. Bellinger, Martina Brueckner +25 more

Single-cell reconstruction and mutation enrichment analysis identifies dysregulated cardiomyocyte and endothelial cells in congenital heart disease

Physiological Genomics(2023)10.1152/physiolgenomics.00070.2023

N/A

0DataRank · unranked

8 citations

Binte Zehra, Sharon Nandkishore, Shermin Sharafat, Faiza Kader, Nasna Nassir +12 more

Machine Learning to Infer Neurocognitive Testing Scores Among Adolescents and Young Adults with Congenital Heart Disease

Research Square(2025)10.21203/rs.3.rs-6787532/v1

N/A

0DataRank · unranked

0 citations

Sheng He, Heather Adams, Evdokia Anagnostou, David C. Bellinger, Martina Brueckner +19 more

De novo damaging variants associated with congenital heart diseases contribute to the connectome

Scientific Reports(2020)10.1038/s41598-020-63928-2

N/A

0DataRank · unranked

60 citations

Dina Ferdman, Joshua A. Copel, Dustin Scheinost, Veronika Shabanova, Martina Brueckner +3 more

Quantifying concordant genetic effects of de novo mutations on multiple disorders

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.06.13.448234

N/A

0DataRank · unranked

1 citations

Lin Hou, Yu Shi, Sheng Chih Jin, Xue Zeng, Boyang Li +5 more

Network Assisted Analysis of De Novo Variants Using Protein-Protein Interaction Information Identified 46 Candidate Genes for Congenital Heart Disease

medRxiv(2021)10.1101/2021.11.30.21267069

N/A

0DataRank · unranked

0 citations

Wei Jiang, Weilai Dong, Hongyu Li, Sheng Chih Jin, Martina Brueckner +2 more

Mutation spectrum of congenital heart disease in a consanguineous Turkish population

Molecular Genetics & Genomic Medicine(2022)10.1002/mgg3.1944

N/A

0DataRank · unranked

13 citations

Hande Kaymakçalan, Sheng Chih Jin, Nicholas S. Diab, İbrahim Cansaran Tanıdır, Ali Seyfi Yalım Yalçın +7 more

Network assisted analysis of de novo variants using protein-protein interaction information identified 46 candidate genes for congenital heart disease

PLoS Genetics(2022)10.1371/journal.pgen.1010252

N/A

0DataRank · unranked

8 citations

Wei Jiang, Weilai Dong, Hongyu Li, Sheng Chih Jin, Martina Brueckner +2 more

Inactivation of Nphp2 in renal epithelial cells drives infantile nephronophthisis like phenotypes in mouse

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.02.10.479981

N/A

0DataRank · unranked

0 citations

Wenyan Xu, Svetlana Makova, Martina Brueckner, Zhaoxia Sun, Yuanyuan Li

Cilia function as calcium-mediated mechanosensors that instruct left-right asymmetry

Science(2023)10.1126/science.abq7317

N/A

0DataRank · unranked

116 citations

Mohammed Mahamdeh, Thai V. Truong, Christopher Nguyen, Scott E. Fraser, Martina Brueckner +3 more

Pleiotropic role of TRAF7 in skull-base meningiomas and congenital heart disease

Proceedings of the National Academy of Sciences(2023)10.1073/pnas.2214997120

N/A

0DataRank · unranked

20 citations

Tanyeri Barak, Leon D. Kaulen, Octavian Henegariu, Sheng Chih Jin, Stephanie Marie Aguilera +25 more

Inactivation of Invs/Nphp2 in renal epithelial cells drives infantile nephronophthisis like phenotypes in mouse

eLife(2023)10.7554/elife.82395

N/A

0DataRank · unranked

10 citations

Wenyan Xu, Svetlana Makova, Martina Brueckner, Zhaoxia Sun, Yuanyuan Li