Jacob Hagen

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 7 papers. Top paper: “Rare variant analysis of 4,241 pulmonary arterial hypertension cases from an international consortium implicate FBLN2 , PDGFD and rare de novo variants in PAH”.

Rare variant analysis of 4,241 pulmonary arterial hypertension cases from an international consortium implicate FBLN2 , PDGFD and rare de novo variants in PAH

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.29.124255

N/A

0DataRank · unranked

4 citations

Emilia M. Swietlik, Carrie L. Welch, Michael W. Pauciulo, Jacob Hagen, Xueya Zhou +19 more

Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

Genome Medicine(2021)10.1186/s13073-021-00891-1

N/A

0DataRank · unranked

86 citations

Emilia M. Swietlik, Carrie L. Welch, Michael W. Pauciulo, Jacob Hagen, Xueya Zhou +89 more

Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH.

White Rose Research Online (University of Leeds, The University of Sheffield, University of York)(2021)10.17863/cam.71232

N/A

0DataRank · unranked

0 citations

Emilia M. Swietlik, Carrie L. Welch, Michael W. Pauciulo, Jacob Hagen, Xueya Zhou +20 more

A homozygous splice variant in ATP5PO, disrupts mitochondrial complex V function and causes Leigh syndrome in two unrelated families

Journal of Inherited Metabolic Disease(2022)10.1002/jimd.12526

N/A

0DataRank · unranked

17 citations

Gaëlle Friocourt, Naïg Guéguen, Marisa W. Friederich, Gérald Le Gac, Volkan Okur +34 more

Identification and validation of candidate risk genes in endocytic vesicular trafficking associated with esophageal atresia and tracheoesophageal fistulas

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100107

N/A

0DataRank · unranked

11 citations

Priyanka Ahimaz, Nicole A. Edwards, Jacob Hagen, Christophe Fauré, Lu Qiao +13 more

Functional dissection of human cardiac enhancers and noncoding de novo variants in congenital heart disease

Nature Genetics(2024)10.1038/s41588-024-01669-y

N/A

0DataRank · unranked

50 citations

Xiaoran Zhang, Sarah U. Morton, Seong Won Kim, Youfei Fan, Joshua M. Gorham +16 more

Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma

Genetics in Medicine(2024)10.1016/j.gim.2024.101125

N/A

0DataRank · unranked

3 citations

Mythily Ganapathi, Yiming Zheng, Kai-Li Tan, Oguz Kanca, Kevin E. Bove +21 more