Tychele Turner

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Evan EichlerProfessor of Genome Sciences, University of WashingtonE-mailová adresa ověřena na: gs.washington.edu
Raphael BernierUniversity of WashingtonE-mailová adresa ověřena na: u.washington.edu
Bradley P CoeLaboratory Scientist, BC Children's and Women's HospitalE-mailová adresa ověřena na: cw.bc.ca
Holly StessmanSenior Fellow, University of WashingtonE-mailová adresa ověřena na: u.washington.edu
Niklas KrummUniversity of Washington - Department of Laboratory MedicineE-mailová adresa ověřena na: uw.edu
Maria Ximena SosaScientist I, Novartis Institutes for Biomedical ResearchE-mailová adresa ověřena na: novartis.com
Vasyl PihurSnap, IncE-mailová adresa ověřena na: snapchat.com
Stephan J. SandersProfessor, Oxford and UCSFE-mailová adresa ověřena na: ucsf.edu
Richard L HuganirProfessor of Neuroscience, Johns Hopkins University School of MedicineE-mailová adresa ověřena na: jhmi.edu
Nicholas KatsanisGalatea BioE-mailová adresa ověřena na: galatea.bio
Daniel Moreno De Luca, MD MScCASA Research Chair, Associate Professor, University of AlbertaE-mailová adresa ověřena na: ualberta.ca
Matthew StateucsfE-mailová adresa ověřena na: ucsf.edu
Christa Lese MartinChief Scientific Officer, Geisinger; Professor and Director, Autism & DevelopmentalE-mailová adresa ověřena na: geisinger.edu
Harrison BrandAssistant Professor at Harvard Medical School, Massachusetts General Hospital, & Broad InstituteE-mailová adresa ověřena na: mgh.harvard.edu
Rachel KarchinProfessor of Biomedical Engineering, Oncology and Computer Science, Johns Hopkins UniversityE-mailová adresa ověřena na: jhu.edu
David N. CooperProfessor of Human Molecular Genetics, Cardiff University, UKE-mailová adresa ověřena na: cardiff.ac.uk
Christopher DouvilleJohns Hopkins UniversityE-mailová adresa ověřena na: jhmi.edu

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Tychele Turner

Washington University School of Medicine, Department of Genetics

E-mailová adresa ověřena na: wustl.edu - Domovská stránka

genomics genetics autism neurodevelopmental disorders sequencing


Název Seřadit podle citací Seřadit podle roku Seřadit podle názvu	Citace Citace	Rok
Excess of rare, inherited truncating mutations in autism N Krumm, TN Turner, C Baker, L Vives, K Mohajeri, K Witherspoon, A Raja, BP ... Nature Genetics, 2015	666	2015
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases HAF Stessman, B Xiong, BP Coe, T Wang, K Hoekzema, M Fenckova, ... Nature genetics 49 (4), 515-526, 2017	575	2017
De novo genic mutations among a Chinese autism spectrum disorder cohort T Wang, H Guo, B Xiong, HAF Stessman, H Wu, BP Coe, TN Turner, Y Liu, ... Nature communications 7 (1), 13316, 2016	393	2016
Genomic Patterns of De Novo Mutation in Simplex Autism TN Turner, BP Coe, DE Dickel, K Hoekzema, BJ Nelson, MC Zody, ... Cell 171 (3), 710-722. e12, 2017	376	2017
Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA TN Turner, F Hormozdiari, MH Duyzend, SA McClymont, PW Hook, ... The American Journal of Human Genetics 98 (1), 58-74, 2016	331	2016
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes X Zhou, P Feliciano, C Shu, T Wang, I Astrovskaya, JB Hall, JU Obiajulu, ... Nature genetics 54 (9), 1305-1319, 2022	250	2022
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes P Feliciano, X Zhou, I Astrovskaya, TN Turner, T Wang, L Brueggeman, ... NPJ genomic medicine 4 (1), 19, 2019	223	2019
Single-cell epigenomics reveals mechanisms of human cortical development RS Ziffra, CN Kim, JM Ross, A Wilfert, TN Turner, M Haeussler, ... Nature 598 (7879), 205-213, 2021	214	2021
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains MR Geisheker, G Heymann, T Wang, BP Coe, TN Turner, HAF Stessman, ... Nature neuroscience 20 (8), 1043-1051, 2017	189	2017
Loss of δ-catenin function in severe autism TN Turner, K Sharma, EC Oh, YP Liu, RL Collins, MX Sosa, DR Auer, ... Nature 520 (7545), 51-56, 2015	181	2015
Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders (Nature Communications,(2020), 11, 1,(4932), 10.1038/s41467-020-18723-y) T Wang, K Hoekzema, D Vecchio, H Wu, A Sulovari, BP Coe, ... Nature Communications 11 (1), 2020	176	2020
Molecular Genetic Anatomy and Risk Profile of Hirschsprung’s Disease JM Tilghman, AY Ling, TN Turner, MX Sosa, N Krumm, S Chatterjee, ... New England Journal of Medicine 380 (15), 1421-1432, 2019	171	2019
Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications AB Wilfert, A Sulovari, TN Turner, BP Coe, EE Eichler Genome Medicine 9, 1-16, 2017	152	2017
denovo-db: a compendium of human de novo variants TN Turner, Q Yi, N Krumm, J Huddleston, K Hoekzema, HAF Stessman, ... Nucleic Acids Research 45 (D1), D804-D811, 2017	142	2017
Sex-Based Analysis of De Novo Variants in Neurodevelopmental Disorders TN Turner, AB Wilfert, TE Bakken, RA Bernier, MR Pepper, Z Zhang, ... The American Journal of Human Genetics 105 (6), 1274-1285, 2019	132	2019
Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes H Guo, MH Duyzend, BP Coe, C Baker, K Hoekzema, J Gerdts, TN Turner, ... Genetics in Medicine 21 (7), 1611-1620, 2019	128	2019
Recent ultra-rare inherited variants implicate new autism candidate risk genes AB Wilfert, TN Turner, SC Murali, PH Hsieh, A Sulovari, T Wang, BP Coe, ... Nature genetics 53 (8), 1125-1134, 2021	120	2021
Affected kindred analysis of human X chromosome exomes to identify novel X-linked intellectual disability genes TS Niranjan, C Skinner, M May, T Turner, R Rose, R Stevenson, ... PloS one 10 (2), e0116454, 2015	74	2015
Clinical phenotype of ASD-associated DYRK1A haploinsufficiency RK Earl, TN Turner, HC Mefford, CM Hudac, J Gerdts, EE Eichler, ... Molecular autism 8, 1-15, 2017	71	2017
The autism spectrum phenotype in ADNP syndrome AB Arnett, CL Rhoads, K Hoekzema, TN Turner, J Gerdts, AS Wallace, ... Autism Research 11 (9), 1300-1310, 2018	66	2018

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