Timothy W. Yu

Also affiliated with Boston Children's Hospital, Howard Hughes Medical Institute, Harvard University, Dana-Farber/Boston Children's Cancer and Blood Disorders Center

Biochemistry, Genetics and Molecular BiologyNeuroscience

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 23 papers. Top paper: “Shared receptors in axon guidance: SAX-3/Robo signals via UNC-34/Enabled and a Netrin-independent UNC-40/DCC function”.

Shared receptors in axon guidance: SAX-3/Robo signals via UNC-34/Enabled and a Netrin-independent UNC-40/DCC function

Nature Neuroscience(2002)10.1038/nn956

N/A

7.3DataRank · unranked

161 citations

Joe C. Hao, Wendell Lim, Marc Tessier-Lavigne, Cornelia I. Bargmann, Timothy W. Yu

A framework for individualized splice-switching oligonucleotide therapy

Nature(2023)10.1038/s41586-023-06277-0

N/A

5.0DataRank · unranked

158 citations

Sijae Woo, Claudio M. de Gusmão, Boxun Zhao, Diana Chin, Renata L. DiDonato +24 more

Children’s rare disease cohorts: an integrative research and clinical genomics initiative

npj Genomic Medicine(2020)10.1038/s41525-020-0137-0

N/A

1.4DataRank · unranked

69 citations

Nicholas LeCompte, Mary M. Carmack, Andrew Quitadamo, Lily Wang, Meredith Park +16 more

Recent ultra-rare inherited variants implicate new autism candidate risk genes

Nature Genetics(2021)10.1038/s41588-021-00899-8

N/A

0.749DataRank · unranked

146 citations

Tychele N. Turner, Shwetha C. Murali, PingHsun Hsieh, Arvis Sulovari, Tianyun Wang +38 more

Contribution and therapeutic implications of retroelement insertions in ataxia telangiectasia

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.09.008

N/A

0.471DataRank · unranked

12 citations

Minh Anh Nguyen, Sijae Woo, Jin‐Kuk Kim, Timothy W. Yu, Eunjung Alice Lee +1 more

Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder

Scientific Reports(2020)10.1038/s41598-020-70656-0

N/A

0.464DataRank · unranked

21 citations

Guzman Sánchez‐Schmitz, Ryan N. Doan, R. Sean Hill, Maria H. Chahrour, Bhaven K. Mehta +9 more

Quantifying Downstream Healthcare Utilization in Studies of Genomic Testing

Value in Health(2020)10.1016/j.jval.2020.01.017

N/A

0.416DataRank · unranked

15 citations

Dmitry Dukhovny, Kathryn A. Phillips, Alan H. Beggs, Robert C. Green, Richard B. Parad +27 more

Moving away from one disease at a time: Screening, trial design, and regulatory implications of novel platform technologies

American Journal of Medical Genetics Part C Seminars in Medical Genetics(2023)10.1002/ajmg.c.32031

N/A

0.373DataRank · unranked

11 citations

Philip J. Brooks, Dwight D. Koeberl, Amy Brower, Aaron J. Goldenberg, Robert C. Green +5 more

ATM-deficiency induced microglial activation promotes neurodegeneration in Ataxia-Telangiectasia

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.09.09.459619

N/A

0.336DataRank · unranked

6 citations

Didem Demirbas, Junho Kim, Ailsa M. Jeffries, Allie K. Tolles, Junseok Park +6 more

Implementation of rapid genomic sequencing in safety-net neonatal intensive care units: protocol for the VIrtual GenOme CenteR (VIGOR) proof-of-concept study

BMJ Open(2024)10.1136/bmjopen-2023-080529

N/A

0.334DataRank · unranked

6 citations

Sonia Hills, Jessica Douglas, Vanessa Young, Casie A. Genetti, Monica H. Wojcik +5 more

Medical Evaluation of Unanticipated Monogenic Disease Risks Identified through Newborn Genomic Screening: Findings from the BabySeq Project

medRxiv(2022)10.1101/2022.03.18.22272284

N/A

0.241DataRank · unranked

4 citations

Nidhi Shah, Casie A. Genetti, Timothy W. Yu, Bethany Zettler, Talia S. Schwartz +13 more

Contributors

Genomic and Personalized Medicine(2013)10.1016/b978-0-12-382227-7.00124-5

N/A

0DataRank · unranked

0 citations

Minhaz Uddin Ahmed, Sun Hee Ahn, R. Rand Allingham, Jude Alsarraj, Matthew L. Anderson +228 more

Deletions in the CDKL5 5′ untranslated region lead to CDKL5 deficiency disorder

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63843

N/A

0DataRank · unranked

2 citations

Ralph D. Hector, Lindsay C. Swanson, Aubrie Soucy Verran, Emma Sherrill, Zoë Frazier +20 more

Disruption of RFX family transcription factors causes autism, attention deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior

medRxiv(2020)10.1101/2020.09.09.20187104

N/A

0DataRank · unranked

9 citations

Tojo Nakayama, Jenny Lai, Boxun Zhao, Nikoleta Argyrou, Cynthia S. Gubbels +71 more

Newborn Sequencing in Genomic Medicine and Public Health

UNC Libraries(2020)10.17615/p3y4-3s09

N/A

0DataRank · unranked

0 citations

Stacey Pereira, Sean D. Mooney, Anastasia L. Wise, Jennifer M. Puck, Timothy W. Yu +37 more

Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior

Genetics in Medicine(2021)10.1038/s41436-021-01114-z

N/A

0DataRank · unranked

93 citations

Tojo Nakayama, Jenny Lai, Boxun Zhao, Nikoleta Argyrou, Cynthia S. Gubbels +76 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

Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.05.007

N/A

0DataRank · unranked

55 citations

Nidhi Shah, Casie A. Genetti, Timothy W. Yu, Bethany Zettler, Melissa Kurtz Uveges +12 more

ATM-deficiency-induced microglial activation promotes neurodegeneration in ataxia-telangiectasia

Cell Reports(2023)10.1016/j.celrep.2023.113622

N/A

0DataRank · unranked

35 citations

Didem Demirbas, Junho Kim, Ailsa M. Jeffries, Allie K. Tolles, Junseok Park +6 more

A Multistakeholder Perspective on Advancing Individualized Therapeutics

Clinical Pharmacology & Therapeutics(2023)10.1002/cpt.3030

N/A

0DataRank · unranked

4 citations

Julia Vitarello, Insoo Hyun, Timothy W. Yu, Issam Zineh, Michael Pacanowski

Family genetic risk communication and reverse cascade testing in the BabySeq project

Genetics in Medicine(2024)10.1016/j.gim.2024.101350

N/A

0DataRank · unranked

3 citations

Hadley Stevens Smith, Stacey Pereira, Casie A. Genetti, Amy L. McGuire, Alan H. Beggs +38 more

Epigenomic and phenotypic characterization of DEGCAGS syndrome

European Journal of Human Genetics(2024)10.1038/s41431-024-01702-y

N/A

0DataRank · unranked

6 citations

Denisa Weis, Ingvild Aukrust, Tzung‐Chien Hsieh, Marie Horackova, Julie Paulsen +37 more

“It’s hard to wait”: Provider perspectives on current genomic care in safety-net NICUs

Genetics in Medicine(2024)10.1016/j.gim.2024.101177

N/A

0DataRank · unranked

5 citations

Monica H. Wojcik, Sonia Hills, Jessica Douglas, Pankaj B. Agrawal, Tyler Allcroft +26 more