🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Elsa Leitão

Essen University Hospital

ORCID: 0000-0001-5051-9714

Also affiliated with University of Duisburg-Essen

Biochemistry, Genetics and Molecular BiologyImmunology and Microbiology

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

1in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology
Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 7 papers. Top paper: “Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X”.

Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X

Nature Communications(2022)10.1038/s41467-022-34264-y
N/A
0.574DataRank · unranked
45 citations

Christopher Schröder, Ilaria Parenti, Carine Dalle, Agnès Rastetter, Theresa Kühnel +32 more

Identification and characterization of repeat expansions in neurological disorders: Methodologies, tools, and strategies

Revue Neurologique(2024)10.1016/j.neurol.2024.03.005
N/A
0.470DataRank · unranked
22 citations

C. Schröder, Christel Depienne, Elsa Leitão

De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders

medRxiv(2024)10.1101/2024.04.07.24305438
N/A
0.360DataRank · unranked
10 citations

Ruebena Dawes, Hyung Chul Kim, Sarah L. Stenton, Susan Walker, Alicia Ljungdahl +92 more

Genome-wide case-only analysis of gene-gene interactions with known Parkinson’s disease risk variants reveals link between LRRK2 and SYT10

npj Parkinson s Disease(2023)10.1038/s41531-023-00550-9
N/A
0.360DataRank · unranked
8 citations

Joanne Trinh, Hampton L. Leonard, Sylvie Delcambre, Elsa Leitão, Dongbing Lai +19 more

Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy

Human Genetics(2021)10.1007/s00439-021-02283-2
N/A
0DataRank · unranked
36 citations

Daphné Lehalle, Caroline Nava, Erin Torti, Elsa Leitão, Richard Person +40 more

Repeat Expansions with Small TTTCA Insertions in MARCHF6 Cause Familial Myoclonus without Epilepsy

Movement Disorders(2025)10.1002/mds.30192
N/A
0DataRank · unranked
1 citations

Elsa Leitão, Renate Lunzer, Fabian Kilpert, Sabine Kaya, Claudia Del Gamba +8 more

Saturation genome editing of RNU4-2 reveals distinct dominant and recessive neurodevelopmental disorders

medRxiv(2025)10.1101/2025.04.08.25325442
N/A
0DataRank · unranked
13 citations

Hyung Chul Kim, Ayanfeoluwa Adedeji, Elsa Leitão, Ruebena Dawes, Yuyang Chen +37 more