Tychele N. Turner

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 2%percentile

2.6Author DataRank

Indexed papers

6in 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 6 indexed papers 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2203491119

Top 14%

1.5DataRank

Top 14%73 citations

Chang N. Kim, Trygve E. Bakken, Madelyn A. Gillentine, Barbara Henning, Yafei Mao +94 more

Papers

Driven by 34 papers — median percentile 42. Top paper: “Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders”.

Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2203491119

Top 14%

1.5DataRank

Top 14%73 citations

Chang N. Kim, Trygve E. Bakken, Madelyn A. Gillentine, Barbara Henning, Yafei Mao +94 more

Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p

Nature Genetics(2022)10.1038/s41588-022-01203-y

N/A

1.3DataRank · unranked

55 citations

Emi Ling, Serkan Erdin, Derek J.C. Tai, Rachita Yadav, Jakob Grove +94 more

Single-cell epigenomics reveals mechanisms of human cortical development

Nature(2021)10.1038/s41586-021-03209-8

N/A

0.857DataRank · unranked

301 citations

Chang N. Kim, Jayden Ross, Amy B. Wilfert, Tychele N. Turner, Maximilian Haeussler +12 more

From karyotypes to precision genomics in 9p deletion and duplication syndromes

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100081

Top 24%

0.827DataRank

Top 24%25 citations

Jeffrey K. Ng, Victoria Tate, Ying‐Chen Claire Hou, Yang Cao, Lucinda Antonacci-Fulton +8 more

Whole-genome sequencing reveals individual and cohort level insights into chromosome 9p syndromes

Genome Medicine(2025)10.1186/s13073-025-01563-0

Top 58%

0.269DataRank

Top 58%5 citations

Eleanor I. Sams, Rachel Slaugh, Sandra Crocker, Emily Cordova Hurtado, Sophia Tracy +66 more

Sequence variants in HECTD1 result in a variable neurodevelopmental disorder

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.01.001

N/A

0.241DataRank · unranked

4 citations

Elias Oxman, Hieu D. Hoang, Wu‐Lin Charng, Tanvitha Kotla, Weimin Yuan +49 more

Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism

Human Genomics(2021)10.1186/s40246-021-00342-3

N/A

0DataRank · unranked

35 citations

Tristan J. Hayeck, Zhang Cheng, Sumantra Chatterjee, Brandon J. Mannion, Marta Byrska-Bishop +30 more

Altered neuronal physiology, development, and function associated with a common chromosome 15 duplication involving CHRNA7

BMC Biology(2021)10.1186/s12915-021-01080-7

N/A

0DataRank · unranked

19 citations

Ramachandran Prakasam, Dustin Baldridge, Paul Gontarz, Bo Zhang, Fumihiko Urano +7 more

Genetic counseling as preventive intervention: toward individual specification of transgenerational autism risk

Journal of Neurodevelopmental Disorders(2021)10.1186/s11689-021-09389-8

N/A

0DataRank · unranked

3 citations

Tychele N. Turner, Elizabeth Forsen, Drew Bolster, Alison R. Marvin, Andrew Whitehouse +4 more

Germline mosaicism of a missense variant in KCNC2 in a multiplex family with autism and epilepsy

medRxiv(2021)10.1101/2021.12.06.21264306

N/A

0DataRank · unranked

1 citations

Teddi Gray, Meghan C. Campbell, Jenny Ekholm, Aaron M. Wenger, William J. Rowell +7 more

ACES: Analysis of Conservation with Expansive Species

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.06.16.448733

N/A

0DataRank · unranked

0 citations

Elvisa Mehinovic, Eleanor I. Sams, Jeffrey K. Ng, Tychele N. Turner, Evin M. Padhi

Can the “female protective effect” liability threshold model explain sex differences in autism spectrum disorder?

Neuron(2022)10.1016/j.neuron.2022.06.020

N/A

0DataRank · unranked

60 citations

Natasha Marrus, Susan E. Maloney, Benjamin Hon Kei Yip, Sven Sandin, Tychele N. Turner +6 more

de novo variant calling identifies cancer mutation signatures in the 1000 Genomes Project

Human Mutation(2022)10.1002/humu.24455

N/A

0DataRank · unranked

17 citations

Pankaj Vats, Elyn Fritz‐Waters, Stephanie Sarkar, Eleanor I. Sams, Evin M. Padhi +12 more

Germline mosaicism of a missense variant in KCNC2 in a multiplex family with autism and epilepsy characterized by long‐read sequencing

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62743

N/A

0DataRank · unranked

13 citations

Teddi Gray, Meghan C. Campbell, Jenny Ekholm, Aaron M. Wenger, William J. Rowell +7 more

Quantitative determination of SLC2A1 variant functional effects in GLUT1 deficiency syndrome

Annals of Clinical and Translational Neurology(2023)10.1002/acn3.51767

N/A

0DataRank · unranked

8 citations

Brian X. León-Ricardo, Kevin McCall, Elvisa Mehinovic, Kristin Engelstad, Vincent Huynh +10 more

Acorn: an R package for de novo variant analysis

BMC Bioinformatics(2023)10.1186/s12859-023-05457-z

N/A

0DataRank · unranked

4 citations

Tychele N. Turner

HAT: de novo variant calling for highly accurate short-read and long-read sequencing data

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.27.525940

N/A

0DataRank · unranked

3 citations

Tychele N. Turner, Jeffrey K. Ng

HAT: de novo variant calling for highly accurate short-read and long-read sequencing data

Bioinformatics(2024)10.1093/bioinformatics/btad775

N/A

0DataRank · unranked

12 citations

Tychele N. Turner, Jeffrey K. Ng

Human-specific gene expansions contribute to brain evolution

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.09.26.615256

N/A

0DataRank · unranked

5 citations

José M. Uribe‐Salazar, Gulhan Kaya, Ricardo Valdarrago, Aarthi Sekar, Nicholas K. Haghani +13 more

Proteome-Wide Assessment of Clustering of Missense Variants in Neurodevelopmental Disorders Versus Cancer

medRxiv(2024)10.1101/2024.02.02.24302238

N/A

0DataRank · unranked

4 citations

Yilin Chen, Titilope M. Akinwe, Hillary B. Heins, Elvisa Mehinovic, Yoonhoo Chang +5 more

Proteome-wide assessment of differential missense variant clustering in neurodevelopmental disorders and cancer

Cell Genomics(2025)10.1016/j.xgen.2025.100807

N/A

0DataRank · unranked

4 citations

Yilin Chen, Titilope M. Akinwe, Hillary B. Heins, Elvisa Mehinovic, Yoonhoo Chang +7 more

Investigating the neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies

Nature Communications(2025)10.1038/s41467-025-65556-8

N/A

0DataRank · unranked

3 citations

Janelle E. Stanton, Geeske M. van Woerden, Amélie Bosc-Rosati, Tzung‐Chien Hsieh, Lise Bray +95 more

CNPI: Rapid Analyses of Human Copy Number Data

Journal of Molecular Biology(2025)10.1016/j.jmb.2025.169313

N/A

0DataRank · unranked

2 citations

Tychele N. Turner, Jack Ustanik

Generation and characterization of a knockout mouse of an enhancer of EBF3

Biology Open(2025)10.1242/bio.062070

N/A

0DataRank · unranked

1 citations

Janine M. Wotton, Alexander O. D. Gulka, Crystal Burke, Jeffrey K. Ng, Ibrahim Bah +8 more

Generation and Characterization of a Knockout Mouse of an Enhancer of EBF3

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.01.09.631762

N/A

0DataRank · unranked

1 citations

Janine M. Wotton, Alexander O. D. Gulka, Crystal Burke, Jeffrey K. Ng, Ibrahim Bah +8 more

Example Input Data for HAT-FLEX

Zenodo (CERN European Organization for Nuclear Research)(2025)10.5281/zenodo.17602490

Top 100%

0DataRank

Top 100%0 citations

Tychele N. Turner

Example Input Data for HAT-FLEX

Zenodo (CERN European Organization for Nuclear Research)(2025)10.5281/zenodo.17602491

Top 100%

0DataRank

Top 100%0 citations

Tychele N. Turner

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Nature Communications(2020)10.1038/s41467-020-18723-y

N/A

0DataRank · unranked

217 citations

Kendra Hoekzema, Davide Vecchio, Huidan Wu, Arvis Sulovari, Bradley P. Coe +95 more

Proteins linked to autosomal dominant and autosomal recessive disorders harbor characteristic rare missense mutation distribution patterns

10.1101/018648

N/A

0DataRank · unranked

0 citations

Christopher Douville, Dewey Kim, Peter D. Stenson, David N. Cooper, Aravinda Chakravarti +2 more

Precise breakpoint detection in a patient with 9p– syndrome

Molecular Case Studies(2020)10.1101/mcs.a005348

N/A

0DataRank · unranked

12 citations

Eleanor I. Sams, Dustin Baldridge, Milinn Kremitzki, Daniel Wegner, Tina Lindsay +4 more

De Novo Mutation in an Enhancer of EBF3 in simplex autism

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.08.28.270751

N/A

0DataRank · unranked

2 citations

Tristan J. Hayeck, Brandon J. Mannion, Sumantra Chatterjee, Marta Byrska-Bishop, Rajeeva Musunuri +16 more

Copy numbers of 45S and 5S ribosomal DNA arrays lack meaningful correlation in humans

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.06.189753

N/A

0DataRank · unranked

0 citations

Tychele N. Turner, Christine Queitsch, Ashley N. Hall

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

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

N/A

0DataRank · unranked

144 citations

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

Thousands of high-quality sequencing samples fail to show meaningful correlation between 5S and 45S ribosomal DNA arrays in humans

Scientific Reports(2021)10.1038/s41598-020-80049-y

N/A

0DataRank · unranked

54 citations

Tychele N. Turner, Christine Queitsch, Ashley N. Hall

Tychele N. Turner

Indexed papers

Top data-sharing exemplar

Papers