🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Afshin Saffari

Boston Children's Hospital

ORCID: 0000-0003-4119-7519

Also affiliated with Heidelberg University, University Hospital Heidelberg

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 11 papers. Top paper: “High-content screening identifies a small molecule that restores AP-4-dependent protein trafficking in neuronal models of AP-4-associated hereditary spastic paraplegia”.

High-content screening identifies a small molecule that restores AP-4-dependent protein trafficking in neuronal models of AP-4-associated hereditary spastic paraplegia

Nature Communications(2024)10.1038/s41467-023-44264-1
N/A
0.624DataRank · unranked
23 citations

Barbara Brechmann, Cedric Böger, Wardiya Afshar Saber, Hellen Jumo, Dosh Whye +14 more

Early‐Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST

Movement Disorders(2022)10.1002/mds.29225
N/A
0.464DataRank · unranked
21 citations

Afshin Saffari, Melanie Kellner, Marion Döbler‐Neumann, Catherine Jordan, Siddharth Srivastava +13 more

Plasma Neurofilament Light Chain Is Elevated in Adaptor Protein Complex 4‐Related Hereditary Spastic Paraplegia

Movement Disorders(2023)10.1002/mds.29524
N/A
0.373DataRank · unranked
11 citations

Afshin Saffari, M. L. ZIEGLER, Catherine Jordan, Amy Tam, So Young Kim +12 more

High-Content Small Molecule Screen Identifies a Novel Compound That Restores AP-4-Dependent Protein Trafficking in Neuronal Models of AP-4-Associated Hereditary Spastic Paraplegia

Research Square(2023)10.21203/rs.3.rs-3036166/v1
N/A
0.104DataRank · unranked
1 citations

Barbara Brechmann, Cedric Boeger, Wardiya Afshar Saber, Hellen Jumo, Dosh Whye +14 more

Natural History and Developmental Trajectories of Individuals With Disease-Causing Variants in STXBP1

Neurology(2023)10.1212/wnl.0000000000207550
N/A
0DataRank · unranked
11 citations

Jan H. Driedger, Julie Xian, Afshin Saffari, Pia Zacher, Bigna K. Bölsterli +49 more

Quantitative natural history modeling of HPDL-related disease based on cross-sectional data reveals genotype-phenotype correlations

Genetics in Medicine(2024)10.1016/j.gim.2024.101349
N/A
0DataRank · unranked
12 citations

Amy Tam, Silja Richter, Vicente Quiroz, Luca Schierbaum, Afshin Saffari +2 more

The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15

Brain(2022)10.1093/brain/awac391
N/A
0DataRank · unranked
24 citations

Melanie Kellner, Catherine Jordan, Helena Rosengarten, Alisa Mo, Bo Zhang +29 more

Biallelic variants in RINT1 present as early-onset pure hereditary spastic paraplegia

Journal of Clinical Investigation(2024)10.1172/jci178919
N/A
0DataRank · unranked
3 citations

Laura Planas‐Serra, Abigail Sveden, Amy Tam, Hyo‐Min Kim, Umar Zubair +10 more

De novovariants cause complex symptoms in HSP-ATL1(SPG3A) and uncover genotype–phenotype correlations

Human Molecular Genetics(2022)10.1093/hmg/ddac182
N/A
0DataRank · unranked
18 citations

Afshin Saffari, Catherine Jordan, Siddharth Srivastava, Craig Blackstone, Darius Ebrahimi‐Fakhari +1 more

Novel CAPN1 missense variants in complex hereditary spastic paraplegia with early‐onset psychosis

Annals of Clinical and Translational Neurology(2022)10.1002/acn3.51531
N/A
0DataRank · unranked
7 citations

Afshin Saffari, Hellen Jumo, M. L. ZIEGLER, Oleksandr Strelko, Catherine A. Brownstein +6 more

The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders

Brain(2023)10.1093/brain/awad039
N/A
0DataRank · unranked
12 citations

Tracy Lau, Homa Tajsharghi, Ehsan Ghayoor Karimiani, Ariana Kariminejad, Yichao Yu +95 more