Detelina Grozeva

Also affiliated with University of Wales

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: “Rare pathogenic variants in WNK3 cause X-linked intellectual disability”.

Rare pathogenic variants in WNK3 cause X-linked intellectual disability

Genetics in Medicine(2022)10.1016/j.gim.2022.05.009

N/A

0.416DataRank · unranked

15 citations

Jinwei Zhang, Thomas Besnard, Alfonso Caro‐Llopis, Xue Zeng, Stephanie M. Robert +75 more

Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia

UNC Libraries(2020)10.17615/8m0s-na92

N/A

0DataRank · unranked

0 citations

John A. McGrath, Pamela Sklar, Gerald Nestadt, David J. Cutler, Paula Wolyniec +25 more

Microduplications of 16p11.2 are associated with schizophrenia

UNC Libraries(2020)10.17615/zwts-m549

N/A

0DataRank · unranked

0 citations

Jaya Ganesh, Detelina Grozeva, Vladimir Makarov, Abhishek Bhandari, Ravinesh A. Kumar +27 more

MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelopmental Disorder with Severe Dystonia

Movement Disorders(2022)10.1002/mds.29147

N/A

0DataRank · unranked

11 citations

Robert Spaull, Smrithi Salian, Katy Barwick, Esther Meyer, Juan Zhen +32 more