Wendy H. Raskind

Pacific Northwest Diabetes Research Institute

Also affiliated with University of Miami, University of Washington, University of Washington Medical Center, University of Miami Hospital

Biochemistry, Genetics and Molecular BiologyPsychologyNeuroscience

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 9 papers. Top paper: “Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome”.

Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome

Annals of Clinical and Translational Neurology(2023)10.1002/acn3.51786

N/A

0.241DataRank · unranked

4 citations

Ghayda Mirzaa, Elizabeth Blue, Giuseppe Albano, Danny E. Miller, Aimee Allworth +28 more

Evidence for involvement of GNB1L in autism

UNC Libraries(2020)10.17615/xax8-6a47

N/A

0DataRank · unranked

0 citations

Ellen M. Wijsman, Ming T. Tsuang, Mark Matsushita, Youngmee Sul, Annette Estes +14 more

Familial Idiopathic Basal Ganglia Calcification: A Father-Son Dyad Demonstrate Heterogeneity of Presentation and Disease Progression

Archives of Clinical Neuropsychology(2021)10.1093/arclin/acab026

N/A

0DataRank · unranked

1 citations

Thomas D. Bird, Donghui Chen, Shu‐Ching Hu, Wendy H. Raskind, Emily H. Trittschuh +1 more

Protein Kinase Cγ Mutations Drive Spinocerebellar Ataxia Type 14 by Impairing Autoinhibition

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.06.24.449810

N/A

0DataRank · unranked

0 citations

Timothy R. Baffi, Alexandr P. Kornev, Maya T. Kunkel, Mario Malfavon, Donghui Chen +9 more

Defects in lysosomal function and lipid metabolism in human microglia harboring a TREM2 loss of function mutation

Acta Neuropathologica(2023)10.1007/s00401-023-02568-y

N/A

0DataRank · unranked

72 citations

Shih‐Feng You, Farzaneh S. Mirfakhar, Sidhartha Mahali, Bryan Bollman, Mariana Acquarone +18 more

Dual diagnosis of UQCRFS1-related mitochondrial complex III deficiency and recessive GJA8-related cataracts

Rare(2024)10.1016/j.rare.2024.100040

N/A

0DataRank · unranked

3 citations

Samuel J. Huang, Alyna Khan, Katie Golden‐Grant, Brenna Boyd, Elisabeth A. Rosenthal +37 more

Assessing Long‐Term Neurologic Outcomes in SAMD9L ‐Related Ataxia‐Pancytopenia Syndrome

Movement Disorders Clinical Practice(2024)10.1002/mdc3.14038

N/A

0DataRank · unranked

0 citations

Donghui Chen, Wendy H. Raskind, William B. Slayton, S. H. Subramony, Joyce Severance +3 more

Mutations in the SIGMAR1 gene cause a distal hereditary motor neuropathy phenotype mimicking ALS: Report of two novel variants

Neuromuscular Disorders(2020)10.1016/j.nmd.2020.05.005

N/A

0DataRank · unranked

17 citations

Donghui Chen, Wendy H. Raskind, Thomas D. Bird, T. Maxwell

Joint exome and metabolome analysis in individuals with dyslexia: Evidence for associated dysregulations of olfactory perception and autoimmune functions

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.06.27.600448

N/A

0DataRank · unranked

0 citations

Xiaojian Shi, Haiwei Gu, Yookyung Kim, Wendy H. Raskind, Beate Peter +2 more