Tychele Turner

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Evan EichlerProfessor of Genome Sciences, University of WashingtonAdresse e-mail validée de gs.washington.edu
Raphael BernierUniversity of WashingtonAdresse e-mail validée de u.washington.edu
Bradley P CoeLaboratory Scientist, BC Children's and Women's HospitalAdresse e-mail validée de cw.bc.ca
Holly StessmanSenior Fellow, University of WashingtonAdresse e-mail validée de u.washington.edu
Niklas KrummUniversity of Washington - Department of Laboratory MedicineAdresse e-mail validée de uw.edu
Maria Ximena SosaScientist I, Novartis Institutes for Biomedical ResearchAdresse e-mail validée de novartis.com
Vasyl PihurSnap, IncAdresse e-mail validée de snapchat.com
Stephan J. SandersProfessor, Oxford and UCSFAdresse e-mail validée de ucsf.edu
Richard L HuganirProfessor of Neuroscience, Johns Hopkins University School of MedicineAdresse e-mail validée de jhmi.edu
Nicholas KatsanisGalatea BioAdresse e-mail validée de galatea.bio
Daniel Moreno De Luca, MD MScCASA Research Chair, Associate Professor, University of AlbertaAdresse e-mail validée de ualberta.ca
Matthew StateucsfAdresse e-mail validée de ucsf.edu
Christa Lese MartinChief Scientific Officer, Geisinger; Professor and Director, Autism & DevelopmentalAdresse e-mail validée de geisinger.edu
Harrison BrandAssistant Professor at Harvard Medical School, Massachusetts General Hospital, & Broad InstituteAdresse e-mail validée de mgh.harvard.edu
Rachel KarchinProfessor of Biomedical Engineering, Oncology and Computer Science, Johns Hopkins UniversityAdresse e-mail validée de jhu.edu
David N. CooperProfessor of Human Molecular Genetics, Cardiff University, UKAdresse e-mail validée de cardiff.ac.uk
Christopher DouvilleJohns Hopkins UniversityAdresse e-mail validée de jhmi.edu

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Tychele Turner

Washington University School of Medicine, Department of Genetics

Adresse e-mail validée de wustl.edu - Page d'accueil

genomics genetics autism neurodevelopmental disorders sequencing


Titre Trier par citations Trier par année Trier par titre	Citée par Citée par	Année
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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