Puneeth H. Somashekar

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: “Multilocus disease-causing genomic variations for Mendelian disorders: role of systematic phenotyping and implications on genetic counselling”.

Multilocus disease-causing genomic variations for Mendelian disorders: role of systematic phenotyping and implications on genetic counselling

European Journal of Human Genetics(2021)10.1038/s41431-021-00933-7

N/A

0DataRank · unranked

43 citations

Divya Udyawar, Parneet Kaur, Suvasini Sharma, Narayanaswamy Suresh, Sheela Nampoothiri +12 more

Bi‐allelic missense variant, p. Ser35Leu in EXOSC1 is associated with pontocerebellar hypoplasia

Clinical Genetics(2021)10.1111/cge.13928

N/A

0DataRank · unranked

33 citations

Parneet Kaur, Joshi Stephen, Vishal Singh Guleria, Rajagopal Kadavigere, Katta M. Girisha +4 more

Growth and neurodevelopmental disorder with arthrogryposis, microcephaly and structural brain anomalies caused by Bi-allelic partial deletion of SMPD4 gene

Journal of Human Genetics(2021)10.1038/s10038-021-00981-3

N/A

0DataRank · unranked

10 citations

Puneeth H. Somashekar, Parneet Kaur, Samarth Kulshrestha, Vedam L. Ramprasad, Sakthivel Murugan +3 more

Biallelic start loss variant, c. 1A > G in GCSH is associated with variant nonketotic hyperglycinemia

Clinical Genetics(2021)10.1111/cge.13970

N/A

0DataRank · unranked

9 citations

Puneeth H. Somashekar, Malavika Hebbar, Rajagopal Kadavigere, B. K. Praveen, Katta M. Girisha +2 more