Shereen G. Ghosh

Also affiliated with Howard Hughes Medical Institute, University of California San Diego, Rady Children's Hospital-San Diego

MedicineBiochemistry, 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 5 papers. Top paper: “Loss of NARS1 impairs progenitor proliferation in cortical brain organoids and leads to microcephaly”.

Loss of NARS1 impairs progenitor proliferation in cortical brain organoids and leads to microcephaly

Nature Communications(2020)10.1038/s41467-020-17454-4

N/A

0DataRank · unranked

88 citations

Zhen Li, David Sievert, Desirée E.C. Smith, Marisa I. Mendes, Dillon Y. Chen +10 more

Loss of the neural-specific BAF subunit ACTL6B relieves repression of early response genes and causes recessive autism

Proceedings of the National Academy of Sciences(2020)10.1073/pnas.1908238117

N/A

0DataRank · unranked

68 citations

Lu Wang, A. Krokhotin, Jessica J. Walsh, Hongjie Li, Hirotaka Shoji +24 more

A relatively common homozygous TRAPPC4 splicing variant is associated with an early-infantile neurodegenerative syndrome

European Journal of Human Genetics(2020)10.1038/s41431-020-00717-5

N/A

0DataRank · unranked

18 citations

Marcello Scala, Christian Beetz, Guy Helman, Valentina Stanley, Xiaoxu Yang +42 more

Biallelic variants in HPDL, encoding 4-hydroxyphenylpyruvate dioxygenase-like protein, lead to an infantile neurodegenerative condition

Genetics in Medicine(2020)10.1038/s41436-020-01010-y

N/A

0DataRank · unranked

37 citations

Sangmoon Lee, Rudy Fabunan, Guoliang Chai, Maha S. Zaki, Ghada M. H. Abdel‐Salam +25 more

Biallelic hypomorphic mutations in HEATR5B, encoding HEAT repeat-containing protein 5B, in a neurological syndrome with pontocerebellar hypoplasia

European Journal of Human Genetics(2021)10.1038/s41431-021-00832-x

N/A

0DataRank · unranked

11 citations

Martin W. Breuss, Zinayida Schlachetzki, Guoliang Chai, Danica Ross, Valentina Stanley +7 more