Tychele N Turner

ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 27

Top Venues

Bioinformatics (Oxford, England)

medRxiv : the preprint server for health sciences

Genome biology and evolution

European journal of human genetics : EJHG

Washington University School of Medicine

Johns Hopkins School of Medicine (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Washington University School of Medicine Sep 01 2019

United States

Assistant Professor :: Genetics

University of Washington - Aug 15 2019

United States

Senior Research Fellow :: Genome Sciences

Johns Hopkins School of Medicine

United States

Graduate Student :: McKusick-Nathans Institute of Genetic Medicine

Education History

Johns Hopkins School of Medicine

United States

PHD :: McKusick-Nathans Institute of Genetic Medicine

Michigan State University

United States

BSC :: Microbiology and Molecular Genetics

Publications

Rodrigo Tzovenos Starosta, Nathaniel Jensen, Sophia Couteranis, Rachel Slaugh, Dawn Easterlin, Victoria Tate, Eleanor I Sams, Kostandin Valle, Titilope Akinwe, Ying-Chen Claire Hou, Tychele N Turner, F Sessions Cole, Jeffrey Milbrandt, Patricia Dickson
Using a new analytic approach for genotyping and phenotyping chromosome 9p deletion syndrome. European journal of human genetics : EJHG 32 (9) (2024)
Rodrigo Tzovenos Starosta, Nathaniel Jensen, Sophia Couteranis, Rachel Slaugh, Dawn Easterlin, Victoria Tate, Eleanor I Sams, Kostandin Valle, Titilope Akinwe, Ying-Chen Claire Hou, Tychele N Turner, F Sessions Cole, Jeffrey Milbrandt, Patricia Dickson
Using a new analytic approach for genotyping and phenotyping chromosome 9p deletion syndrome. European journal of human genetics : EJHG (2024)
Tristan J Hayeck, Yang Li, Timothy L Mosbruger, Jonathan P Bradfield, Adam G Gleason, George Damianos, Grace Tzun-Wen Shaw, Jamie L Duke, Laura K Conlin, Tychele N Turner, Marcelo A Fernández-Viña, Mahdi Sarmady, Dimitri S Monos
The Impact of Patterns in Linkage Disequilibrium and Sequencing Quality on the Imprint of Balancing Selection. Genome biology and evolution 16 (2) (2024)
Jeffrey K Ng, Tychele N Turner
HAT: de novo variant calling for highly accurate short-read and long-read sequencing data. Bioinformatics (Oxford, England) 40 (1) (2024)
Jeffrey K Ng, Tychele N Turner
HAT: de novo variant calling for highly accurate short-read and long-read sequencing data. Bioinformatics (Oxford, England) 40 (1) (2024)
Tristan J Hayeck, Yang Li, Timothy L Mosbruger, Jonathan P Bradfield, Adam G Gleason, George Damianos, Grace Tzun-Wen Shaw, Jamie L Duke, Laura K Conlin, Tychele N Turner, Marcelo A Fernández-Viña, Mahdi Sarmady, Dimitri S Monos
The Impact of Patterns in Linkage Disequilibrium and Sequencing Quality on the Imprint of Balancing Selection. Genome biology and evolution (2024)
Jeffrey K Ng, Tychele N Turner
HAT: de novo variant calling for highly accurate short-read and long-read sequencing data. Bioinformatics (Oxford, England) 40 (1) (2024)
Jeffrey K Ng, Yilin Chen, Titilope M Akinwe, Hillary B Heins, Elvisa Mehinovic, Yoonhoo Chang, Zachary L Payne, Juana G Manuel, Rachel Karchin, Tychele N Turner
Proteome-Wide Assessment of Clustering of Missense Variants in Neurodevelopmental Disorders Versus Cancer. medRxiv : the preprint server for health sciences (2024)
Jeffrey K Ng, Tychele N Turner
HAT: de novo variant calling for highly accurate short-read and long-read sequencing data. Bioinformatics (Oxford, England) 40 (1) (2024)
Jeffrey K Ng, Tychele N Turner
HAT: de novo variant calling for highly accurate short-read and long-read sequencing data. Bioinformatics (Oxford, England) 40 (1) (2024)
Jeffrey K Ng, Tychele N Turner
HAT: de novo variant calling for highly accurate short-read and long-read sequencing data. Bioinformatics (Oxford, England) 40 (1) (2024)
Jeffrey K Ng, Tychele N Turner
HAT: de novo variant calling for highly accurate short-read and long-read sequencing data. Bioinformatics (Oxford, England) 40 (1) (2024)
Jeffrey K Ng, Yilin Chen, Titilope M Akinwe, Hillary B Heins, Elvisa Mehinovic, Yoonhoo Chang, Zachary L Payne, Juana G Manuel, Rachel Karchin, Tychele N Turner
Proteome-Wide Assessment of Clustering of Missense Variants in Neurodevelopmental Disorders Versus Cancer. medRxiv : the preprint server for health sciences (2024)
Tristan J Hayeck, Yang Li, Timothy L Mosbruger, Jonathan P Bradfield, Adam G Gleason, George Damianos, Grace Tzun-Wen Shaw, Jamie L Duke, Laura K Conlin, Tychele N Turner, Marcelo A Fernández-Viña, Mahdi Sarmady, Dimitri S Monos
The Impact of Patterns in Linkage Disequilibrium and Sequencing Quality on the Imprint of Balancing Selection. Genome biology and evolution 16 (2) (2024)
Sébastien Küry, Janelle E Stanton, Geeske M van Woerden, Tzung-Chien Hsieh, Cory Scott Rosenfelt, Marie-Pier Scott-Boyer, Victoria Most, Tianyun Wang, Jonas Johannes Papendorf, Charlotte de Konink, Wallid Deb, Virginie Vignard, Maja Studencka-Turski, Thomas Besnard, Anna Marta Hajdukowicz, Franziska Thiel, Sophie Möller, Laëtitia Florenceau, Silvestre Cuinat, Sylvain Marsac, Ingrid Wentzensen, Annabelle Tuttle, Cara Forster, Johanna Striesow, Richard Golnik, Damara Ortiz, Laura Jenkins, Jill Anne Rosenfeld, Alban Ziegler, Clara Houdayer, Dominique Bonneau, Erin Torti, Amber Begtrup, Kristin G Monaghan, Sureni V Mullegama, C M L Nienke Volker-Touw, Koen L I van Gassen, Renske Oegema, Mirjam de Pagter, Katharina Steindl, Anita Rauch, Ivan Ivanovski, Kimberly McDonald, Emily Boothe, Andrew Dauber, Janice Baker, Noelle Andrea V Fabie, Raphael A Bernier, Tychele N Turner, Siddharth Srivastava, Kira A Dies, Lindsay Swanson, Carrie Costin, Rebekah K Jobling, John G Pappas, Rachel Rabin, Dmitriy Niyazov, Anne Chun-Hui Tsai, Karen Kovak, David B Beck, May Christine V Malicdan, David R Adams, Lynne Wolfe, Rebecca D Ganetzky, Colleen Muraresku, Davit Babikyan, Zdenek Sedlacek, Miroslava Hancarova, Andrew T Timberlake, Hind Al Saif, Berkley Nestler, Kayla King, M J Hajianpour, Gregory Costain, D'Arcy Prendergast, Chumei Li, David Genevieve, Antonio Vitobello, Arthur Sorlin, Christophe Philippe, Tamar Harel, Ori Toker, Ataf Hussain Sabir, Derek Lim, Mark Hamilton, Lisa Bryson, Elaine Cleary, Sacha Weber, Trevor L Hoffman, Anna Maria Cueto-González, Eduardo Fidel Tizzano, David Gomez Andres, Marta Codina Solà, Athina Ververi, Efterpi Pavlidou, Alexandros Lambropoulos, Kyriakos Garganis, Marlène Rio, Jonathan Levy, Sarah Jurgensmeyer, Anne M McRae, Mathieu Kent Lessard, Maria Daniela D'Agostino, Isabelle De Bie, Meret Wegler, Rami Abou Jamra, Susanne B Kamphausen, Viktoria Bothe, Larissa M Busch, Uwe Völker, Elke Hammer, Kristian Wende, Benjamin Cogné, Bertrand Isidor, Jens Meiler, Amélie Bosc-Rosati, Julien Marcoux, Marie-Pierre Bousquet, Jeremie Poschmann, Frederic Laumonnier, Peter W Hildebrand, Evan E Eichler, Kirsty McWalter, Peter M Krawitz, Arnaud Droit, Ype Elgersma, Andreas Martin Grabrucker, Francois V Bolduc, Stephane Bezieau, Frédéric Ebstein, Elke Krüger
Unveiling the crucial neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies. medRxiv : the preprint server for health sciences (2024)
Jeffrey K Ng, Yilin Chen, Titilope M Akinwe, Hillary B Heins, Elvisa Mehinovic, Yoonhoo Chang, Zachary L Payne, Juana G Manuel, Rachel Karchin, Tychele N Turner
Proteome-Wide Assessment of Clustering of Missense Variants in Neurodevelopmental Disorders Versus Cancer. medRxiv : the preprint server for health sciences (2024)
Xueya Zhou, Pamela Feliciano, Chang Shu, Tianyun Wang, Irina Astrovskaya, Jacob B Hall, Joseph U Obiajulu, Jessica R Wright, Shwetha C Murali, Simon Xuming Xu, Leo Brueggeman, Taylor R Thomas, Olena Marchenko, Christopher Fleisch, Sarah D Barns, LeeAnne Green Snyder, Bing Han, Timothy S Chang, Tychele N Turner, William T Harvey, Andrew Nishida, Brian J O'Roak, Daniel H Geschwind, null null, Jacob J Michaelson, Natalia Volfovsky, Evan E Eichler, Yufeng Shen, Wendy K Chung
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes. Nature genetics 54 (9) (2022)
Tristan J Hayeck, Nicholas Stong, Evan Baugh, Ryan S Dhindsa, Tychele N Turner, Ayan Malakar, Timothy L Mosbruger, Grace Tzun-Wen Shaw, Yuncheng Duan, Iuliana Ionita-Laza, David Goldstein, Andrew S Allen
Ancestry adjustment improves genome-wide estimates of regional intolerance. Genetics 221 (2) (2022)
Jeffrey K Ng, Pankaj Vats, Elyn Fritz-Waters, Stephanie Sarkar, Eleanor I Sams, Evin M Padhi, Zachary L Payne, Shawn Leonard, Marc A West, Chandler Prince, Lee Trani, Marshall Jansen, George Vacek, Mehrzad Samadi, Timothy T Harkins, Craig Pohl, Tychele N Turner
de novo variant calling identifies cancer mutation signatures in the 1000 Genomes Project. Human mutation (2022)
Elvisa Mehinovic, Teddi Gray, Meghan Campbell, Jenny Ekholm, Aaron Wenger, William J Rowell, Ari Grudo, Jane Grimwood, Jonas Korlach, Christina Gurnett, John N Constantino, Tychele N Turner
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 188 (7) (2022)
Evin M Padhi, Tristan J Hayeck, Zhang Cheng, Sumantra Chatterjee, Brandon J Mannion, Marta Byrska-Bishop, Marjolaine Willems, Lucile Pinson, Sylvia Redon, Caroline Benech, Kevin Uguen, Séverine Audebert-Bellanger, Cédric Le Marechal, Claude Férec, Stephanie Efthymiou, Fatima Rahman, Shazia Maqbool, Reza Maroofian, Henry Houlden, Rajeeva Musunuri, Giuseppe Narzisi, Avinash Abhyankar, Riana D Hunter, Jennifer Akiyama, Lauren E Fries, Jeffrey K Ng, Elvisa Mehinovic, Nick Stong, Andrew S Allen, Diane E Dickel, Raphael A Bernier, David U Gorkin, Len A Pennacchio, Michael C Zody, Tychele N Turner
Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism. Human genomics 15 (1) (2021)
Amy B Wilfert, Tychele N Turner, Shwetha C Murali, PingHsun Hsieh, Arvis Sulovari, Tianyun Wang, Bradley P Coe, Hui Guo, Kendra Hoekzema, Trygve E Bakken, Lara H Winterkorn, Uday S Evani, Marta Byrska-Bishop, Rachel K Earl, Raphael A Bernier, null null, Michael C Zody, Evan E Eichler
Recent ultra-rare inherited variants implicate new autism candidate risk genes. Nature genetics 53 (8) (2021)
Ryan S Ziffra, Chang N Kim, Jayden M 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 Jan Nowakowski
Single-cell epigenomics reveals mechanisms of human cortical development. Nature 598 (7879) (2021)
Pamela Feliciano, Xueya Zhou, Irina Astrovskaya, Tychele N Turner, Tianyun Wang, Leo Brueggeman, Rebecca Barnard, Alexander Hsieh, LeeAnne Green Snyder, Donna M Muzny, Aniko Sabo, null null, Richard A Gibbs, Evan E Eichler, Brian J O'Roak, Jacob J Michaelson, Natalia Volfovsky, Yufeng Shen, Wendy K Chung
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes. NPJ genomic medicine 4 (2019)
Madeleine R Geisheker, Gabriel Heymann, Tianyun Wang, Bradley P Coe, Tychele N Turner, Holly A F Stessman, Kendra Hoekzema, Malin Kvarnung, Marie Shaw, Kathryn Friend, Jan Liebelt, Christopher Barnett, Elizabeth M Thompson, Eric A Haan, Hui Guo, Britt-Marie Anderlid, Ann Nordgren, Anna Lindstrand, Geert Vandeweyer, Antonino Alberti, Emanuela Avola, Mirella Vinci, Stefania Giusto, Tiziano Pramparo, Karen Pierce, Srinivasa Nalabolu, Jacob J Michaelson, Zdenek Sedlacek, Gijs W E Santen, Hilde Peeters, Hakon Hakonarson, Eric Courchesne, Corrado Romano, R Frank Kooy, Raphael A Bernier, Magnus Nordenskjöld, Jozef Gecz, Kun Xia, Larry S Zweifel, Evan E Eichler
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains. Nature neuroscience 20 (8) (2017)
Tychele N Turner, Qian Yi, Niklas Krumm, John Huddleston, Kendra Hoekzema, Holly A F Stessman, Anna-Lisa Doebley, Raphael A Bernier, Deborah A Nickerson, Evan E Eichler
denovo-db: a compendium of human de novo variants. Nucleic acids research 45 (D1) (2016)
Tianyun Wang, Hui Guo, Bo Xiong, Holly A F Stessman, Huidan Wu, Bradley P Coe, Tychele N Turner, Yanling Liu, Wenjing Zhao, Kendra Hoekzema, Laura Vives, Lu Xia, Meina Tang, Jianjun Ou, Biyuan Chen, Yidong Shen, Guanglei Xun, Min Long, Janice Lin, Zev N Kronenberg, Yu Peng, Ting Bai, Honghui Li, Xiaoyan Ke, Zhengmao Hu, Jingping Zhao, Xiaobing Zou, Kun Xia, Evan E Eichler
De novo genic mutations among a Chinese autism spectrum disorder cohort. Nature communications 7 (2016)

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Publication Activity (10 Years)

Top Topics

Top Venues

Tychele N Turner