Tanya L. Schwab

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 7 papers. Top paper: “Haploinsufficiency as a disease mechanism in GNB1‐associated neurodevelopmental disorder”.

Haploinsufficiency as a disease mechanism in GNB1‐associated neurodevelopmental disorder

Molecular Genetics & Genomic Medicine(2020)10.1002/mgg3.1477

N/A

0DataRank · unranked

18 citations

Ikuo Masuho, Filippo Pinto e Vairo, Christopher T. Schmitz, Tanya L. Schwab, Karl J. Clark +6 more

A homozygous missense variant in UBE2T is associated with a mild Fanconi anemia phenotype

Haematologica(2020)10.3324/haematol.2020.259275

N/A

0DataRank · unranked

5 citations

Francis P. Lach, Kimberly A. Rickman, Alejandro Ferrer, Abhishek A. Mangaonkar, Tanya L. Schwab +10 more

Characterization of Gene Repression by Designed Transcription Activator-like Effector Dimer Proteins

Biophysical Journal(2020)10.1016/j.bpj.2020.10.007

N/A

0DataRank · unranked

3 citations

Justin P. Peters, Tanya L. Schwab, William J. Phillips, Jordan P. Wallace, Karl J. Clark +2 more

Designed architectural proteins that tune DNA looping in bacteria

Nucleic Acids Research(2021)10.1093/nar/gkab759

N/A

0DataRank · unranked

5 citations

Nicole A. Becker, Robert T. Young, Wilma K. Olson, Justin P. Peters, Tanya L. Schwab +3 more

Designed architectural proteins that tune DNA looping in bacteria

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.06.30.450240

N/A

0DataRank · unranked

0 citations

Nicole A. Becker, Robert T. Young, Wilma K. Olson, Justin P. Peters, Tanya L. Schwab +3 more

Bi-allelic variants in INTS11 are associated with a complex neurological disorder

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.03.012

N/A

0DataRank · unranked

38 citations

Erica L. Macke, Marcello Niceta, Monika Weisz Hubshman, Oguz Kanca, Laura Schultz‐Rogers +95 more

Bi-allelic variants in HMGCR cause an autosomal-recessive progressive limb-girdle muscular dystrophy

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.04.006

N/A

0DataRank · unranked

37 citations

Tanya L. Schwab, Sarah K. Macklin‐Mantia, A. Reghan Foley, Filippo Pinto e Vairo, Davut Pehli̇van +25 more