John P. Schacht

Walter Reed National Military Medical Center

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 2 papers. Top paper: “Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays”.

Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays

European Journal of Human Genetics(2023)10.1038/s41431-023-01434-5

N/A

0.494DataRank · unranked

26 citations

Leticia S. Matsuoka, Michael March, Dong Li, Elly Brokamp, Sara Benito‐Sanz +32 more

Rapid exome sequencing in PICU patients with new-onset metabolic or neurological disorders

Pediatric Research(2020)10.1038/s41390-020-0858-x

N/A

0DataRank · unranked

28 citations

John P. Schacht, Christine Umandap, David Fasel, Chunhua Weng, Joshua Cappell +3 more