Mari Tokita

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 13 papers. Top paper: “Abnormal SCID Newborn Screening and Spontaneous Recovery Associated with a Novel Haploinsufficiency IKZF1 Mutation”.

Abnormal SCID Newborn Screening and Spontaneous Recovery Associated with a Novel Haploinsufficiency IKZF1 Mutation

Journal of Clinical Immunology(2021)10.1007/s10875-021-01035-1

N/A

0.505DataRank · unranked

8 citations

Nicholas J. Gloude, David Dimmock, Mari Tokita, Meredith S. Wright, Sergio D. Rosenzweig +2 more

Genetic evaluation of pediatric pituitary adenomas and USP8-related genotype-phenotype correlations in Cushing’s disease

Pituitary(2025)10.1007/s11102-025-01557-6

N/A

0.165DataRank · unranked

2 citations

Sukhvir Kaur, Justin Lack, Morgan N Similuk, Mayank Tandon, Rajarshi Ghosh +8 more

De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability

Journal of Medical Genetics(2021)10.1136/jmedgenet-2021-107751

N/A

0DataRank · unranked

30 citations

Margot A. Cousin, Nikita R. Dsouza, Thomas D. Challman, Karen E. Wain, Zöe Powis +67 more

A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.08.003

N/A

0DataRank · unranked

171 citations

Laurie D. Smith, Chris M. Kunard, Matthew Bainbridge, Sergey Batalov, Wendy Benson +46 more

Insights into the perinatal phenotype of Kabuki syndrome in infants identified by genome‐wide sequencing

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63097

N/A

0DataRank · unranked

3 citations

Monia Hammer, Mari Tokita, Priyanka Patel, Marilyn C. Jones, Austin Larson +17 more

Response to Grosse et al.

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.05.004

N/A

0DataRank · unranked

1 citations

Laurie D. Smith, Chris M. Kunard, Matthew Bainbridge, Serge Batalov, Wendy Benson +46 more

Case report: Deep sequencing and long-read genome sequencing refine prior genetic analyses in families with apparent gonadal mosaicism in PIK3CD-related activated PI3K delta syndrome

Frontiers in Immunology(2024)10.3389/fimmu.2024.1451212

N/A

0DataRank · unranked

2 citations

Jia Yan, Alex Paul, Mari Tokita, Yan Ding, Rajarshi Ghosh +17 more

Further Personalizing Medicine in Immune Disorders: Genomic Findings and Hematopoietic Cell Transplantation Survival

Transplantation(2025)10.1097/tp.0000000000005504

N/A

0DataRank · unranked

1 citations

Sarah A. Bannon, Jia Yan, Rajarshi Ghosh, Ekaterina Damskey, Breanna Beers +41 more

Cerebral Venous Thrombosis in Previously Healthy Patients with Cryptococcal Meningitis

The Journal of Infectious Diseases(2025)10.1093/infdis/jiaf653

N/A

0DataRank · unranked

1 citations

Jessica C. Hargarten, Brittany Dulek, Francisco Otaizo‐Carrasquero, Winnie Trang, Shelley S. Kalsi +8 more

Genome Sequencing Uncovers Additional Findings in Phelan‐McDermid Syndrome

American Journal of Medical Genetics Part B Neuropsychiatric Genetics(2025)10.1002/ajmg.b.33036

N/A

0DataRank · unranked

0 citations

Morgan N Similuk, Alexandra Hehn, Rylee Duncan, Margaret Pekar, Eliza Gordon‐Lipkin +17 more

An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.10.003

N/A

0DataRank · unranked

191 citations

Michelle M. Clark, Mary Gaughran, Julie A. Cakici, Sara Caylor, Christina Clarke +62 more

Long‐Read Sequencing as a Diagnostic Tool for Primary Ciliary Dyskinesia

Case Reports in Genetics(2025)10.1155/crig/5109434

N/A

0DataRank · unranked

0 citations

Morgan N Similuk, Laura M. Amendola, Katie L. Lewis, Magdalena Walkiewicz, Mari Tokita +3 more

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

UNC Libraries(2020)10.17615/02rz-mz46

N/A

0DataRank · unranked

0 citations

Jane Ranchalis, Mitzi L. Murray, Ann Katherine M. Foreman, Seema M. Jamal, Andrew D. Johnson +27 more