Tiffany Grider

Also affiliated with University of Iowa Health Care

NeuroscienceMedicineBiochemistry, Genetics and Molecular Biology

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 6 papers. Top paper: “A longitudinal study of CMT1A using Rasch analysis based CMT neuropathy and examination scores”.

A longitudinal study of CMT1A using Rasch analysis based CMT neuropathy and examination scores

Neurology(2020)10.1212/wnl.0000000000009035

N/A

0DataRank · unranked

53 citations

Stefan Sillau, Gyula Acsádi, Chelsea Bacon, Kimberly Dooley, Joshua Burns +32 more

Combined clinical, structural and cellular studies discriminate pathogenic and benign TRPV4 variants

Brain(2024)10.1093/brain/awae243

N/A

0DataRank · unranked

7 citations

Linh K. Vo, Do Hoon Kwon, Tiffany Grider, Yasmine S Damayanti, Gage P Kosmanopoulos +17 more

Heterozygous loss-of-function variants in SPTAN1 cause a novel early childhood onset distal myopathy with chronic neurogenic features

medRxiv(2024)10.1101/2024.09.23.24313872

N/A

0DataRank · unranked

3 citations

Liedewei Van de Vondel, Biljana Ermanoska, Alice Monticelli, Arnaud Isapof, Enzo Cohen +33 more

Heterozygous loss-of-function variants in SPTAN1 cause an early childhood onset distal myopathy

Genetics in Medicine(2025)10.1016/j.gim.2025.101399

N/A

0DataRank · unranked

5 citations

Liedewei Van de Vondel, Biljana Ermanoska, Alice Monticelli, Arnaud Isapof, Enzo Cohen +32 more

Charcot-Marie-Tooth disease type 1E: clinical natural history and molecular impact of PMP22 variants

Brain(2025)10.1093/brain/awaf219

N/A

0DataRank · unranked

3 citations

Christopher P. Ptak, Natalya Pashkova, Tiffany Grider, Tabitha A. Peterson, Davide Pareyson +47 more

Gene-Pseudogene Inversions as a Hidden Source of Missing Heritability

medRxiv(2025)10.1101/2025.10.01.25336578

N/A

0DataRank · unranked

0 citations

Stefano Facchini, Arianna Manini, Ricardo Parolin Schnekenberg, Chiara Pisciotta, Stefania Magri +37 more