Giedré Grigelioniené

Also affiliated with Karolinska Institutet

Biochemistry, Genetics and Molecular Biology

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: “Defining the clinical phenotype of Saul–Wilson syndrome”.

Defining the clinical phenotype of Saul–Wilson syndrome

Genetics in Medicine(2020)10.1038/s41436-019-0737-1

N/A

0DataRank · unranked

21 citations

Wadih M. Zein, Laryssa A. Huryn, Andrea Merker, Seth Berger, William G. Wilson +26 more

Lack of GNAS Remethylation During Oogenesis May Be a Cause of Sporadic Pseudohypoparathyroidism Type Ib

The Journal of Clinical Endocrinology & Metabolism(2021)10.1210/clinem/dgab830

N/A

0DataRank · unranked

8 citations

Monica Reyes, Patrick Hanna, Zentaro Kiuchi, Serap Turan, Daniel Zeve +11 more

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

A hypomorphic variant in the translocase of the outer mitochondrial membrane complex subunit TOMM7 causes short stature and developmental delay

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100148

N/A

0DataRank · unranked

18 citations

Dominyka Batkovskyte, Miyuki Kitamura, Maria Shvedova, Yutaro Mihara, Jun Akiba +7 more