Tychele N. Turner

6.4k citations

47 papers · 1.7k indexed · 1 hit paper · h-index 20

Co-authors: Evan E. Eichler Bradley P. Coe Raphael Bernier Niklas Krumm Archana N. Raja Holly A.F. Stessman Aravinda Chakravarti Kendra Hoekzema
Topics: Genomic variations and chromosomal abnormalities (18 papers)Genetics and Neurodevelopmental Disorders (17 papers)Genomics and Rare Diseases (14 papers)
Cited by: Genetics Cognitive Neuroscience Molecular Biology
Journals: Nature New England Journal of Medicine Cell
Partner nations: United States United Kingdom Sweden

In The Last Decade

Tychele N. Turner

43 papers receiving 1.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Excess of rare, inherited truncating mutations in autism

2015 345 citations Tychele N. Turner, Carl Baker et al. profile →

Peers

Countries citing papers authored by Tychele N. Turner

Since Specialization

Citations

This map shows the geographic impact of Tychele N. Turner's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Tychele N. Turner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tychele N. Turner more than expected).

Fields of papers citing papers by Tychele N. Turner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tychele N. Turner. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Tychele N. Turner. The network helps show where Tychele N. Turner may publish in the future.

Co-authorship network of co-authors of Tychele N. Turner

This figure shows the co-authorship network connecting the top 25 collaborators of Tychele N. Turner. A scholar is included among the top collaborators of Tychele N. Turner based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Tychele N. Turner. Tychele N. Turner is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Time trends in the male to female ratio for autism incidence: population based, prospectively collected, birth cohort study 2026 ·BMJ ·(unknown),Henric Winell,(unknown),(unknown),(unknown),(unknown),Kristina Tedroff,Tychele N. Turner,(unknown),(unknown),(unknown),(unknown)	0
2	Human-specific gene expansions contribute to brain evolution 2025 ·Cell ·Daniela C. Soto,(unknown),Gulhan Kaya,(unknown),(unknown),(unknown),Keiko Hino,(unknown),(unknown),(unknown),(unknown),Zoeb N. Jamal,Tychele N. Turner,Eric D. Green,Sergi Simó,Gerald Quon,Aida M. Andrés,Megan Y. Dennis	2
3	Proteome-wide assessment of differential missense variant clustering in neurodevelopmental disorders and cancer 2025 ·Cell Genomics ·(unknown),(unknown),(unknown),Hillary B. Heins,(unknown),(unknown),David H. Gutmann,Christina A. Gurnett,(unknown),(unknown),Rachel Karchin,Tychele N. Turner	1
4	CNPI: Rapid Analyses of Human Copy Number Data 2025 ·Journal of Molecular Biology ·(unknown),Tychele N. Turner	0
5	Examining Sex Differences in Autism Heritability 2024 ·JAMA Psychiatry ·Sven Sandin,Benjamin Hon Kei Yip,Weiyao Yin,Lauren A. Weiss,(unknown),(unknown),John N. Constantino,(unknown),Tychele N. Turner,Natasha Marrus,David H. Gutmann,Stephan Sanders,(unknown)	11
6	HAT: de novo variant calling for highly accurate short-read and long-read sequencing data 2024 ·Bioinformatics ·(unknown),Tychele N. Turner	3
7	Quantitative determination of SLC2A1 variant functional effects in GLUT1 deficiency syndrome 2023 ·Annals of Clinical and Translational Neurology ·Naeimeh Tayebi,(unknown),Kevin McCall,(unknown),Kristin Engelstad,(unknown),Tychele N. Turner,(unknown),(unknown),Paul W. Hruz,Robin S. B. Williams,Darryl C. De Vivo,Vincent Petit,Gabe Haller,Christina A. Gurnett	5
8	Ancestry adjustment improves genome-wide estimates of regional intolerance 2022 ·Genetics ·Tristan J. Hayeck,Nicholas Stong,Evan H. Baugh,Ryan S. Dhindsa,Tychele N. Turner,(unknown),Timothy L. Mosbruger,Grace Tzun-Wen Shaw,(unknown),Iuliana Ionita‐Laza,David B. Goldstein,Andrew S. Allen	2
9	A gap-free genome assembly of Chlamydomonas reinhardtii and detection of translocations induced by CRISPR-mediated mutagenesis 2022 ·Plant Communications ·(unknown),(unknown),Tychele N. Turner,Susan K. Dutcher	20
10	Single-cell epigenomics reveals mechanisms of human cortical development 2021 ·Nature ·Ryan Ziffra,Chang N. Kim,Jayden Ross,Amy B. Wilfert,Tychele N. Turner,Maximilian Haeussler,Alex M. Casella,Pawel F. Przytycki,Kathleen C. Keough,David Shin,Derek Bogdanoff,Anat Kreimer,Katherine S. Pollard,Seth A. Ament,Evan E. Eichler,Nadav Ahituv,Tomasz J. Nowakowski	153
11	Genetic counseling as preventive intervention: toward individual specification of transgenerational autism risk 2021 ·Journal of Neurodevelopmental Disorders ·Natasha Marrus,Tychele N. Turner,(unknown),(unknown),Alison R. Marvin,Andrew Whitehouse,Laura G. Klinger,Christina A. Gurnett,John N. Constantino	3
12	Sex-Based Analysis of De Novo Variants in Neurodevelopmental Disorders 2019 ·The American Journal of Human Genetics ·Tychele N. Turner,Amy B. Wilfert,Trygve E. Bakken,Raphael Bernier,Micah Pepper,Zhancheng Zhang,Rebecca I. Torene,Kyle Retterer,Evan E. Eichler	87
13	Clinical Phenotypes of Carriers of Mutations in CHD8 or Its Conserved Target Genes 2019 ·Biological Psychiatry ·Jennifer S. Beighley,Caitlin M. Hudac,Anne B. Arnett,(unknown),Jennifer Gerdts,Arianne S. Wallace,Heather C. Mefford,Kendra Hoekzema,Tychele N. Turner,Brian J. O’Roak,Evan E. Eichler,Raphael Bernier	19
14	Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes 2018 ·Genetics in Medicine ·Hui Guo,Michael Duyzend,Bradley P. Coe,Carl Baker,Kendra Hoekzema,Jennifer Gerdts,Tychele N. Turner,Michael C. Zody,Jennifer S. Beighley,Shwetha C. Murali,Bradley J. Nelson,Michael J. Bamshad,Deborah A. Nickerson,Raphael Bernier,Evan E. Eichler	80
15	Clinical phenotype of ASD-associated DYRK1A haploinsufficiency 2017 ·Molecular Autism ·Rachel K. Earl,Tychele N. Turner,Heather C. Mefford,Caitlin M. Hudac,Jennifer Gerdts,Evan E. Eichler,Raphael Bernier	51
16	Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications 2017 ·Genome Medicine ·Amy B. Wilfert,Arvis Sulovari,Tychele N. Turner,Bradley P. Coe,Evan E. Eichler	91
17	Genomic Patterns of De Novo Mutation in Simplex Autism 2017 ·Cell ·Tychele N. Turner,Bradley P. Coe,Diane E. Dickel,Kendra Hoekzema,Bradley J. Nelson,Michael C. Zody,Zev Kronenberg,Fereydoun Hormozdiari,Archana N. Raja,L Pennacchio,Robert B. Darnell,Evan E. Eichler	208
18	Molecular subtyping and improved treatment of neurodevelopmental disease 2016 ·Genome Medicine ·Holly A.F. Stessman,Tychele N. Turner,Evan E. Eichler	14
19	Affected Kindred Analysis of Human X Chromosome Exomes to Identify Novel X-Linked Intellectual Disability Genes 2015 ·PLoS ONE ·Tejasvi Niranjan,Cindy Skinner,Melanie May,Tychele N. Turner,Rebecca Rose,Roger E. Stevenson,Charles E. Schwartz,Tao Wang	39
20	Proteins linked to autosomal dominant and autosomal recessive disorders harbor characteristic rare missense mutation distribution patterns 2015 ·Human Molecular Genetics ·Tychele N. Turner,Christopher Douville,Dewey Kim,Peter D. Stenson,D.N. Cooper,Aravinda Chakravarti,Rachel Karchin	31

About Tychele N. Turner

Tychele N. Turner is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology, having authored 47 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Genomics and Rare Diseases (14 papers). The work is most often cited by research in Genetics (1.1k citations), Cognitive Neuroscience (530 citations) and Molecular Biology (915 citations). Tychele N. Turner has collaborated with scholars based in United States, United Kingdom and Sweden. Frequent co-authors include Evan E. Eichler, Bradley P. Coe, Raphael Bernier, Niklas Krumm, Archana N. Raja, Holly A.F. Stessman, Aravinda Chakravarti, Kendra Hoekzema, Amy B. Wilfert and Carl Baker. Their work appears in journals such as Nature, New England Journal of Medicine and Cell.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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