Thomas Bast

MedicineBiochemistry, Genetics and Molecular BiologyNeuroscience

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

2in 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 2 indexed papers 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 6 papers. Top paper: “Focal epilepsy in SCN1A‐mutation carrying patients: is there a role for epilepsy surgery?”.

Focal epilepsy in SCN1A‐mutation carrying patients: is there a role for epilepsy surgery?

Developmental Medicine & Child Neurology(2020)10.1111/dmcn.14588

N/A

1.3DataRank · unranked

31 citations

Sophia Varadkar, Thomas Bast, Edouard Hirsch, Karl Strobl, A Simon Harvey +4 more

Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway

Genetics in Medicine(2014)10.1038/gim.2014.22

N/A

0.821DataRank · unranked

238 citations

Vandana Shashi, Matthew Bainbridge, Michael J. Gambello, Thomas Bast, Rebecca Crimian +29 more

Constitutional PIGA mutations cause a novel subtype of hemochromatosis in patients with neurologic dysfunction

Blood(2022)10.1182/blood.2021013519

N/A

0.449DataRank · unranked

19 citations

Oriana Marques, Silvia Colucci, Joachim Kunz, Piotr Fabrowski, Thomas Bast +12 more

Correction: Corrigendum: Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway

Genetics in Medicine(2014)10.1038/gim.2014.61

N/A

0.136DataRank · unranked

1 citations

Vandana Shashi, Matthew N. Bainbridge, Michael J. Gambello, Farah Zahir, Thomas Bast +28 more

Kohlschütter-Tönz Syndrome: Mutations in ROGDI and Evidence of Genetic Heterogeneity

UNC Libraries(2020)10.17615/mb8t-wh97

N/A

0DataRank · unranked

4 citations

Anna Schossig, John Hardy, Katharina Wimmer, Michael B. Tennison, Ian Hayes +25 more

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

Nature Genetics(2023)10.1038/s41588-023-01485-w

N/A

0DataRank · unranked

217 citations

Ciarán Campbell, Siwei Chen, Bassel Abou‐Khalil, Oluyomi M. Adesoji, Zaid Afawi +95 more