Conrad C. Weihl

Biochemistry, Genetics and Molecular BiologyNeuroscienceMedicine

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 5%percentile

0.460Author 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Expert panel curation of 31 genes in relation to limb girdle muscular dystrophy

Annals of Clinical and Translational Neurology(2024)10.1002/acn3.52127

Top 60%

0.252DataRank

Top 60%4 citations

Shannon McNulty, Courtney L Thaxton, Marwa Elnagheeb, Emma Owens, May Flowers +25 more

Papers

Driven by 28 papers — median percentile 38. Top paper: “Client processing is altered by novel myopathy-causing mutations in the HSP40 J domain”.

Client processing is altered by novel myopathy-causing mutations in the HSP40 J domain

PLoS ONE(2020)10.1371/journal.pone.0234207

N/A

0.516DataRank · unranked

14 citations

Conrad C. Weihl, Heather L. True, Melanie Y. Pullen

Expert panel curation of 31 genes in relation to limb girdle muscular dystrophy

Annals of Clinical and Translational Neurology(2024)10.1002/acn3.52127

Top 60%

0.252DataRank

Top 60%4 citations

Shannon McNulty, Courtney L Thaxton, Marwa Elnagheeb, Emma Owens, May Flowers +25 more

Clinical Trial Readiness in Limb Girdle Muscular Dystrophy R1 (LGMDR1): A GRASP Consortium Study

Annals of Clinical and Translational Neurology(2025)10.1002/acn3.70049

Top 65%

0.208DataRank

Top 65%3 citations

Lindsay N. Alfano, Aileen Jones, Amanda Butler, Linda Lowes, M. Iammarino +24 more

Myositis associated anti-NT5C1A autoantibody in clinical practice

medRxiv(2020)10.1101/2020.03.25.20043760

N/A

0DataRank · unranked

0 citations

Andrew R. Findlay, Namita Goyal, Sarah Robinson, Jonathan Cauchi, Yessar Hussain +9 more

Neuronal VCP loss of function recapitulates FTLD-TDP pathology

Cell Reports(2021)10.1016/j.celrep.2021.109399

N/A

0DataRank · unranked

49 citations

Jiang Zhu, Jason D. Ulrich, Abdallah M. Eteleeb, Andrew D. Sauerbeck, Sydney J. Reitz +15 more

Clinical utility of anti‐cytosolic 5’‐nucleotidase 1A antibody in idiopathic inflammatory myopathies

Annals of Clinical and Translational Neurology(2021)10.1002/acn3.51294

N/A

0DataRank · unranked

32 citations

Andrew R. Findlay, Namita Goyal, Sarah Robinson, Jonathan Cauchi, Yessar Hussain +9 more

Patient reported quality of life in limb girdle muscular dystrophy

Neuromuscular Disorders(2021)10.1016/j.nmd.2021.11.002

N/A

0DataRank · unranked

13 citations

Kameron Bates, Jeffrey Statland, Conrad C. Weihl, Peter B. Kang, Linda Lowes +6 more

The p97-UBXD8 complex modulates ER-Mitochondria contact sites by modulating membrane lipid saturation and composition

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.12.08.471763

N/A

0DataRank · unranked

3 citations

Joao A. Paulo, Yuecheng Xi, Ian Kline, Jiang Zhu, Christoph S. Clemen +5 more

Myopathy mutations in DNAJB6 slow conformer specific substrate processing that is corrected by NEF modulation

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.12.22.473881

N/A

0DataRank · unranked

0 citations

Michael Rau, Jil Daw, James A. J. Fitzpatrick, Conrad C. Weihl, Heather L. True +1 more

Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy

Orphanet Journal of Rare Diseases(2022)10.1186/s13023-022-02172-5

N/A

0DataRank · unranked

36 citations

Allison Peck, Lindsay N. Alfano, Kenneth I. Berger, M. James, Nupur Ghoshal +50 more

LGMDD1 natural history and phenotypic spectrum: Implications for clinical trials

Annals of Clinical and Translational Neurology(2022)10.1002/acn3.51709

N/A

0DataRank · unranked

11 citations

Sarah Robinson, Stephanie Poelker, Michelle Seiffert, Rocío Bengoechea, Conrad C. Weihl +1 more

Disease-associated mutations within the yeast DNAJB6 homolog Sis1 slow conformer-specific substrate processing and can be corrected by the modulation of nucleotide exchange factors

Nature Communications(2022)10.1038/s41467-022-32318-9

N/A

0DataRank · unranked

8 citations

Michael Rau, Jil Daw, James A. J. Fitzpatrick, Conrad C. Weihl, Heather L. True +1 more

Myopathy mutations in DNAJB6 slow conformer specific substrate processing that is corrected by NEF modulation

Research Square(2022)10.21203/rs.3.rs-1041146/v1

N/A

0DataRank · unranked

0 citations

Michael Rau, Jil Daw, James A. J. Fitzpatrick, Conrad C. Weihl, Heather L. True +1 more

The p97-UBXD8 complex regulates ER-Mitochondria contact sites by altering membrane lipid saturation and composition

Nature Communications(2023)10.1038/s41467-023-36298-2

N/A

0DataRank · unranked

46 citations

Joao A. Paulo, Yuecheng Xi, Ian Kline, Jiang Zhu, Christoph S. Clemen +5 more

Comprehensive functional characterization of SGCB coding variants predicts pathogenicity in limb-girdle muscular dystrophy type R4/2E

Journal of Clinical Investigation(2023)10.1172/jci168156

N/A

0DataRank · unranked

19 citations

Jackson Wilborn, Sara K. Pittman, Jil Daw, Jorge Alonso‐Pérez, Jordi Díaz‐Manera +3 more

An autosomal-dominant childhood-onset disorder associated with pathogenic variants in VCP

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.10.007

N/A

0DataRank · unranked

8 citations

Jil Daw, Diana Huynh, Mengcheng Wu, Benjamin C. Creekmore, William Burns +30 more

Provisional practice recommendation for the management of myopathy in VCP‐associated multisystem proteinopathy

Annals of Clinical and Translational Neurology(2023)10.1002/acn3.51760

N/A

0DataRank · unranked

9 citations

Allison Peck, Teresinha Evangelista, Gerald Pfeffer, Leo Wang, Jordi Díaz‐Manera +15 more

Genetic deletion of skeletal muscle iPLA2γ results in mitochondrial dysfunction, muscle atrophy and alterations in whole-body energy metabolism

iScience(2023)10.1016/j.isci.2023.106895

N/A

0DataRank · unranked

7 citations

Beverly Gibson Dilthey, Shaoping Guan, Harold F. Sims, Sara K. Pittman, Amy L. Keith +4 more

Seeding-competent TDP-43 persists in human patient and mouse muscle

Science Translational Medicine(2024)10.1126/scitranslmed.adp5730

N/A

0DataRank · unranked

20 citations

Sara K. Pittman, Jil Daw, Chiseko Ikenaga, Sheng Chen, Dhruva D. Dhavale +8 more

Elevated VCP ATPase Activity Correlates With Disease Onset in Multisystem Proteinopathy-1

Neurology Genetics(2024)10.1212/nxg.0000000000200191

N/A

0DataRank · unranked

7 citations

Andrew R. Findlay, Shan Li, Feng Wang, Marianela Schiava, Jil Daw +4 more

VCP Inhibition Augments NLRP3 Inflammasome Activation

Inflammation(2024)10.1007/s10753-024-02013-6

N/A

0DataRank · unranked

5 citations

Dhruva D. Dhavale, Paul T. Kotzbauer, Conrad C. Weihl, Ankita Sharma

Seeding competent TDP-43 persists in human patient and mouse muscle

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.04.03.587918

N/A

0DataRank · unranked

2 citations

Sara K. Pittman, Jil Daw, Chiseko Ikenaga, Sheng Chen, Dhruva D. Dhavale +8 more

Expert Panel Curation of 31 Genes in Relation to Limb Girdle Muscular Dystrophy

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.05.03.592369

N/A

0DataRank · unranked

0 citations

Shannon McNulty, Courtney L Thaxton, Marwa Elnagheeb, Emma Owens, May Flowers +25 more

Myofibrillar myopathy: towards a mechanism-based definition as a Z-disk-opathy

Current Opinion in Neurology(2025)10.1097/wco.0000000000001397

N/A

0DataRank · unranked

4 citations

Conrad C. Weihl, Michio Inoue

Mutations in Hsp40 co-chaperone change the unique canonical inter-domain interactions stimulating LGMDD1 myopathy

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.05.02.651952

N/A

0DataRank · unranked

0 citations

Geetika Aggarwal, Mahapatra Anshuman Jaysingh, Daniel C. Chen, Jil Daw, Conrad C. Weihl +2 more

Mutations in Hsp40 co-chaperone change the canonical interdomain interactions stimulating LGMDD1 myopathy

Journal of Biological Chemistry(2025)10.1016/j.jbc.2025.110945

N/A

0DataRank · unranked

0 citations

Geetika Aggarwal, Mahapatra Anshuman Jaysingh, Daniel C. Chen, Jil Daw, Conrad C. Weihl +2 more

Inhibition of DNAJ-HSP70 interaction improves strength in muscular dystrophy

Journal of Clinical Investigation(2020)10.1172/jci136167

N/A

0DataRank · unranked

30 citations

Andrew R. Findlay, Ankan K. Bhadra, Hao Shao, Kevin C. Stein, Sara K. Pittman +5 more

Phenotypic diversity in an international Cure VCP Disease registry

Orphanet Journal of Rare Diseases(2020)10.1186/s13023-020-01551-0

N/A

0DataRank · unranked

23 citations

Andrew R. Findlay, Michelle Seiffert, Allison Peck, Nathan Peck, Nicholas E. Johnson +3 more

Conrad C. Weihl

Indexed papers

Top data-sharing exemplar

Papers