Ieva Mičule

Biochemistry, Genetics and Molecular BiologyNeuroscienceMedicine

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 3 papers. Top paper: “Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders”.

Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders

npj Genomic Medicine(2022)10.1038/s41525-021-00273-x

N/A

0DataRank · unranked

26 citations

Shuyang Zhang, Sigrún Hallgrímsdóttir, Yuzhi Zuo, Xiaoxin Li, Dominyka Batkovskyte +31 more

Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype–phenotype correlations and common mechanisms

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63247

N/A

0DataRank · unranked

41 citations

Justin Blair, Batsal Devkota, Sierra Fortunato, Dinah Clark, Audrey Lawrence +92 more

The phenotypic spectrum of PTCD3 deficiency

JIMD Reports(2024)10.1002/jmd2.12424

N/A

0DataRank · unranked

0 citations

Eissa Faqeih, Namik Kaya, Zita Krūmiņa, Johannes A. Mayr, Ieva Mičule +8 more