Lisa Worgan

Also affiliated with Royal Prince Alfred Hospital, Sydney Local Health District

NeuroscienceBiochemistry, 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: “Homozygous splice-variants in human ARV1 cause GPI-anchor synthesis deficiency”.

Homozygous splice-variants in human ARV1 cause GPI-anchor synthesis deficiency

Molecular Genetics and Metabolism(2020)10.1016/j.ymgme.2020.02.005

N/A

0DataRank · unranked

24 citations

Minal Menezes, Yiran Guo, Scott McLean, Håkon Håkonarson, Felicity Collins +13 more

Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.003

N/A

0DataRank · unranked

42 citations

Somayeh Bakhtiari, Ashley P.L. Marsh, Rauan Kaiyrzhanov, Matias Wagner, Sheetal Shetty +95 more

Neonatal-lethal dilated cardiomyopathy due to a homozygous LMOD2 donor splice-site variant

European Journal of Human Genetics(2022)10.1038/s41431-022-01043-8

N/A

0DataRank · unranked

19 citations

Lisa Worgan, Jessika Iwanski, Christopher T. Pappas, Himanshu Joshi, Jared M. Churko +7 more

Two New Families and a Literature Review of ELOVL4-Associated Spinocerebellar Ataxia Type 34

The Cerebellum(2023)10.1007/s12311-023-01522-8

N/A

0DataRank · unranked

10 citations

Kathleen Le Marquand, Mark R. Davis, G. Michael Hálmagyi, Avi Fellner, Ramesh K. Narayanan +6 more