Ali Fatemi

Also affiliated with Johns Hopkins University, Johns Hopkins Medicine

MedicineBiochemistry, 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

1in 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 1 indexed paper 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 →

Papers

Driven by 22 papers. Top paper: “Expansion sequencing: Spatially precise in situ transcriptomics in intact biological systems”.

Expansion sequencing: Spatially precise in situ transcriptomics in intact biological systems

Science(2021)10.1126/science.aax2656

N/A

0.902DataRank · unranked

408 citations

Daniel R. Goodwin, Anubhav Sinha, Asmamaw T. Wassie, Fei Chen, Evan R. Daugharthy +164 more

Three-dimensional imaging mass cytometry for highly multiplexed molecular and cellular mapping of tissues and the tumor microenvironment

Nature Cancer(2021)10.1038/s43018-021-00301-w

N/A

0.812DataRank · unranked

224 citations

Raúl Catena, Alaz Özcan, Alex Plüss, H. Raza Ali, M. Al Sa’d +74 more

International Recommendations for the Diagnosis and Management of Patients With Adrenoleukodystrophy

Neurology(2022)10.1212/wnl.0000000000201374

N/A

0.745DataRank · unranked

143 citations

Wouter J. C. van Ballegoij, Eric J. Mallack, Keith Van Haren, Wolfgang Köhler, Ettore Salsano +23 more

MRI surveillance of boys with X‐linked adrenoleukodystrophy identified by newborn screening: Meta‐analysis and consensus guidelines

Journal of Inherited Metabolic Disease(2020)10.1002/jimd.12356

N/A

0.659DataRank · unranked

80 citations

Bela R. Turk, Helena Yan, Carrie Price, Michelle Demetres, Ann B. Moser +18 more

Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann‐Steiner syndrome

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62124

N/A

0.644DataRank · unranked

72 citations

Ian M. Campbell, Margaret Harr, Nina B. Gold, Dong Li, Hans T. Björnsson +95 more

Longitudinal natural history studies based on real-world data in rare diseases: Opportunity and a novel approach

Molecular Genetics and Metabolism(2024)10.1016/j.ymgme.2024.108453

N/A

0.489DataRank · unranked

25 citations

Anjana Sevagamoorthy, Omar Sherbini, Jamie L. Fraser, Joshua L. Bonkowsky, Francesco Gavazzi +18 more

Consensus guidelines for the monitoring and management of metachromatic leukodystrophy in the United States

Cytotherapy(2024)10.1016/j.jcyt.2024.03.487

N/A

0.489DataRank · unranked

25 citations

Joshua L. Bonkowsky, Jaap Jan Boelens, Eric J. Mallack, Rebecca C. Ahrens‐Nicklas, John Bernat +27 more

Targeted Brain Delivery of Dendrimer-4-Phenylbutyrate Ameliorates Neurological Deficits in a Long-Term ABCD1-Deficient Mouse Model of X-Linked Adrenoleukodystrophy

Neurotherapeutics(2022)10.1007/s13311-022-01311-x

N/A

0.373DataRank · unranked

11 citations

Özgül Gök, Sophia N. Tomlinson, Anjali Sharma, Ann B. Moser, Sujatha Kannan +3 more

De novo variants in DENND5B cause a neurodevelopmental disorder

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.02.001

N/A

0.345DataRank · unranked

9 citations

Valeria Tomati, Matteo P. Ferla, Mariateresa Lena, Julie S. Cohen, Ali Fatemi +94 more

Optimizing Multiparametric MRI Protocols for Prostate Cancer Detection: A Comprehensive Assessment Aligned with PI‐RADS Guidelines

Health Science Reports(2024)10.1002/hsr2.70172

N/A

0.241DataRank · unranked

4 citations

Ali Fatemi, Aida Karami, Sepehr Ghanavati, Durjoy D. Dhruba, Mohammad H. Negarestanian +1 more

Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner Syndrome

Molecular Genetics and Metabolism(2021)10.1016/s1096-7192(21)00373-5

N/A

0.104DataRank · unranked

1 citations

Ian M. Campbell, Margaret Harr, Nina B. Gold, Dong Li, Hans T. Björnsson +95 more

A phase I study of oral vitamin D3 in boys with X-linked adrenoleukodystrophy

medRxiv(2022)10.1101/2021.12.28.21267861

N/A

0DataRank · unranked

1 citations

Kristen Cunanan, Avni Awani, Meng Gu, Dalia Peña, Lindsay C. Chromik +14 more

Clinical and functional consequences of GRIA variants in patients with neurological diseases

Cellular and Molecular Life Sciences(2023)10.1007/s00018-023-04991-6

N/A

0DataRank · unranked

19 citations

Riley E. Perszyk, Nana Liu, Yuchen Xu, Subhrajit Bhattacharya, Gil Shaulsky +25 more

Mutations in DARS2 result in global dysregulation of mRNA metabolism and splicing

Scientific Reports(2023)10.1038/s41598-023-40107-7

N/A

0DataRank · unranked

10 citations

B. M. O’Brien, Albert S. Fine, Ming Ying, Ali Fatemi, Christina L. Nemeth +1 more

Cation leak through the ATP1A3 pump causes spasticity and intellectual disability

Brain(2023)10.1093/brain/awad124

N/A

0DataRank · unranked

13 citations

Cristina Moreno Vadillo, Seth Berger, Timothy Lotze, Marwan Shinawi, Javaher Poupak +24 more

A Phase 1 Study of Oral Vitamin D 3 in Boys and Young Men With X-Linked Adrenoleukodystrophy

Neurology Genetics(2023)10.1212/nxg.0000000000200061

N/A

0DataRank · unranked

8 citations

Kristen Cunanan, Avni Awani, Meng Gu, Dalia Peña, Lindsay C. Chromik +14 more

Presymptomatic Lesion in Childhood Cerebral Adrenoleukodystrophy

Neurology(2022)10.1212/wnl.0000000000200571

N/A

0DataRank · unranked

16 citations

Keith Van Haren, Anna C Torrey, Stephanie I. W. van de Stadt, Marc Engelen, Gerald V. Raymond +3 more

The pathogenesis of, and pharmacological treatment for, Canavan disease

Drug Discovery Today(2022)10.1016/j.drudis.2022.05.019

N/A

0DataRank · unranked

29 citations

John R. Moffett, Man Amanat, Ali Fatemi, Takashi Tsukamoto, Aryan M.A. Namboodiri +2 more

Developmental delay can precede neurologic regression in early onset metachromatic leukodystrophy

Molecular Genetics and Metabolism(2024)10.1016/j.ymgme.2024.108521

N/A

0DataRank · unranked

8 citations

Samuel Groeschel, Chloe Grzyb, Russell D’Aiello, Francesco Gavazzi, Omar Sherbini +43 more

Clinically Important Endpoints in Individuals With Leukodystrophy: A Multisite Study

Annals of the Child Neurology Society(2025)10.1002/cns3.70025

N/A

0DataRank · unranked

0 citations

Sarah Woidill, Russell D’Aiello, Amina Khan, Jacob McCann, Mark Ramos +27 more

Wearable sensors detect impaired gait and coordination in LBSL during remote assessments

Annals of Clinical and Translational Neurology(2022)10.1002/acn3.51509

N/A

0DataRank · unranked

13 citations

Miriam L. Kaufman, Jordan Goodman, Bela R. Turk, Amy J. Bastian, Doris Lin +3 more

Novel variants in KAT6B spectrum of disorders expand our knowledge of clinical manifestations and molecular mechanisms

Molecular Genetics & Genomic Medicine(2021)10.1002/mgg3.1809

N/A

0DataRank · unranked

14 citations

Jessica Kianmahd, Meghna Singh, Maria F. Palafox, Angela Wei, Kathryn Elliott +40 more