Christina Peroutka

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 4 papers. Top paper: “Sequence variants in HECTD1 result in a variable neurodevelopmental disorder”.

Sequence variants in HECTD1 result in a variable neurodevelopmental disorder

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.01.001

N/A

0.241DataRank · unranked

4 citations

Elias Oxman, Hieu D. Hoang, Wu‐Lin Charng, Tanvitha Kotla, Weimin Yuan +49 more

Compound heterozygous DAW1 variants reveal tissue-specific roles in left-right patterning and congenital heart disease without primary ciliary dyskinesia

(2026)10.64898/2026.01.27.26344789

N/A

0DataRank · unranked

0 citations

Anburaj Jeyaraj, Shruti Bedekar, Venkatramanan G. Rao, Shelby C White, Matthew J Thomas +8 more

Necrotizing enterocolitis totalis complicates an infantile presentation of ARL6IP1-related spastic paraplegia 61

Journal of Pediatric Surgery Case Reports(2021)10.1016/j.epsc.2021.102063

N/A

0DataRank · unranked

0 citations

Michael C. Spaeder, Christina Peroutka, Daniel E. Levin, Emily K. Ninmer

Yao syndrome in a child with C2 deficiency

The Journal of Allergy and Clinical Immunology In Practice(2024)10.1016/j.jaip.2024.08.018

N/A

0DataRank · unranked

3 citations

Geoffrey Hall, Rachel L. Randell, Monica G. Lawrence, Aarat Patel, Christina Peroutka +3 more