Turner, Tychele N.: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

1

The autism spectrum phenotype in ADNP syndrome

Arnett, Anne B., Rhoads, Candace L., Hoekzema, Kendra, Turner, Tychele N., Gerdts, Jennifer, Wallace, Arianne S., Bedrosian-Sermone, Sandra, Eichler, Evan E., Bernier, Raphael A.

Journal:

Autism Research

Year:

2018

Language:

english

File:

PDF, 320 KB

english, 2018

2

Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes

Feliciano, Pamela, Zhou, Xueya, Astrovskaya, Irina, Turner, Tychele N., Wang, Tianyun, Brueggeman, Leo, Barnard, Rebecca, Hsieh, Alexander, Snyder, LeeAnne Green, Muzny, Donna M., Sabo, Aniko, Gibbs,

Journal:

npj Genomic Medicine

Year:

2019

Language:

english

File:

PDF, 1.40 MB

english, 2019

3

Clinical phenotype of ASD-associated DYRK1A haploinsufficiency

Earl, Rachel K., Turner, Tychele N., Mefford, Heather C., Hudac, Caitlin M., Gerdts, Jennifer, Eichler, Evan E., Bernier, Raphael A.

Journal:

Molecular Autism

Year:

2017

Language:

english

File:

PDF, 2.29 MB

english, 2017

4

Sex-Based Analysis of De Novo Variants in Neurodevelopmental Disorders

Turner, Tychele N., Wilfert, Amy B., Bakken, Trygve E., Bernier, Raphael A., Pepper, Micah R., Zhang, Zhancheng, Torene, Rebecca I., Retterer, Kyle, Eichler, Evan E.

Journal:

The American Journal of Human Genetics

Year:

2019

File:

PDF, 2.13 MB

2019

5

Plot protein: visualization of mutations

Journal:

Journal of Clinical Bioinformatics

Year:

2013

Language:

english

File:

PDF, 157 KB

english, 2013

6

De novo genic mutations among a Chinese autism spectrum disorder cohort

Wang, Tianyun, Guo, Hui, Xiong, Bo, Stessman, Holly A.F., Wu, Huidan, Coe, Bradley P., Turner, Tychele N., Liu, Yanling, Zhao, Wenjing, Hoekzema, Kendra, Vives, Laura, Xia, Lu, Tang, Meina, Ou, Jianju

Journal:

Nature Communications

Year:

2016

Language:

english

File:

PDF, 584 KB

english, 2016

7

Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains

Geisheker, Madeleine R, Heymann, Gabriel, Wang, Tianyun, Coe, Bradley P, Turner, Tychele N, Stessman, Holly A F, Hoekzema, Kendra, Kvarnung, Malin, Shaw, Marie, Friend, Kathryn, Liebelt, Jan, Barnett,

Journal:

Nature Neuroscience

Year:

2017

Language:

english

File:

PDF, 1.26 MB

english, 2017

8

The autism spectrum phenotype in ADNP syndrome

Arnett, Anne B., Rhoads, Candace L., Hoekzema, Kendra, Turner, Tychele N., Gerdts, Jennifer, Wallace, Arianne S., Bedrosian-Sermone, Sandra, Eichler, Evan E., Bernier, Raphael A.

Journal:

Autism Research

Year:

2018

File:

PDF, 320 KB

2018

9

The Role of De Novo Noncoding Regulatory Mutations in Neurodevelopmental Disorders

Turner, Tychele N., Eichler, Evan E.

Journal:

Trends in Neurosciences

Year:

2018

Language:

english

File:

PDF, 3.76 MB

english, 2018

10

Rapid and efficient human mutation detection using a bench-top next-generation DNA sequencer

Qian Jiang, Tychele Turner, Maria X. Sosa, Ankit Rakha, Stacey Arnold, Aravinda Chakravarti

Journal:

Year:

2012

Language:

english

File:

PDF, 343 KB

english, 2012

11

Molecular subtyping and improved treatment of neurodevelopmental disease

Stessman, Holly A. F., Turner, Tychele N., Eichler, Evan E.

Journal:

Genome Medicine

Year:

2016

Language:

english

File:

PDF, 499 KB

english, 2016

12

Affected Kindred Analysis of Human X Chromosome Exomes to Identify Novel X-Linked Intellectual Disability Genes

Niranjan, Tejasvi S., Skinner, Cindy, May, Melanie, Turner, Tychele, Rose, Rebecca, Stevenson, Roger, Schwartz, Charles E., Wang, Tao, Bardoni, Barbara

Journal:

Year:

2015

Language:

english

File:

PDF, 1.87 MB

english, 2015

13

Clinical phenotypes of carriers of mutations in CHD8 or its conserved target genes

Beighley, Jennifer S., Hudac, Caitlin M., Arnett, Anne B., Peterson, Jessica L., Gerdts, Jennifer, Wallace, Arianne S., Mefford, Heather C., Hoekzema, Kendra, Turner, Tychele N., O’Roak, Brian J., Eic

Journal:

Biological Psychiatry

Year:

2019

Language:

english

File:

PDF, 2.37 MB

english, 2019

14

Revealing rate-limiting steps in complex disease biology: The crucial importance of studying rare, extreme-phenotype families

Chakravarti, Aravinda, Turner, Tychele N.

Journal:

Year:

2016

Language:

english

File:

PDF, 495 KB

english, 2016

15

Quantifying and Modeling Birth Order Effects in Autism

Turner, Tychele, Pihur, Vasyl, Chakravarti, Aravinda, Whitehouse, Andrew

Journal:

Year:

2011

Language:

english

File:

PDF, 605 KB

english, 2011

16

Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA

Turner, Tychele N., Hormozdiari, Fereydoun, Duyzend, Michael H., McClymont, Sarah A., Hook, Paul W., Iossifov, Ivan, Raja, Archana, Baker, Carl, Hoekzema, Kendra, Stessman, Holly A., Zody, Michael C.,

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 1.54 MB

english, 2016

17

denovo-db: a compendium of human de novo variants

Turner, Tychele N., Yi, Qian, Krumm, Niklas, Huddleston, John, Hoekzema, Kendra, F. Stessman, Holly A., Doebley, Anna-Lisa, Bernier, Raphael A., Nickerson, Deborah A., Eichler, Evan E.

Journal:

Nucleic Acids Research

Year:

2017

Language:

english

File:

PDF, 2.50 MB

english, 2017

18

Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes

Guo, Hui, Duyzend, Michael H., Coe, Bradley P., Baker, Carl, Hoekzema, Kendra, Gerdts, Jennifer, Turner, Tychele N., Zody, Michael C., Beighley, Jennifer S., Murali, Shwetha C., Nelson, Bradley J., Ba

Journal:

Genetics in Medicine

Year:

2018

Language:

english

File:

PDF, 570 KB

english, 2018

19

Precise breakpoint detection in a patient with 9pâ syndrome

Ng, Jeffrey, Sams, Eleanor, Baldridge, Dustin, Kremitzki, Milinn, Wegner, Daniel J., Lindsay, Tina, Fulton, Robert, Cole, F. Sessions, Turner, Tychele N.

Journal:

Molecular Case Studies

Year:

2020

File:

PDF, 2.30 MB

2020

20

Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications

Wilfert, Amy B., Sulovari, Arvis, Turner, Tychele N., Coe, Bradley P., Eichler, Evan E.

Journal:

Genome Medicine

Year:

2017

Language:

english

File:

PDF, 1.77 MB

english, 2017

21

Loss of δ-catenin function in severe autism

Turner, Tychele N., Sharma, Kamal, Oh, Edwin C., Liu, Yangfan P., Collins, Ryan L., Sosa, Maria X., Auer, Dallas R., Brand, Harrison, Sanders, Stephan J., Moreno-De-Luca, Daniel, Pihur, Vasyl, Plona,

Journal:

Year:

2015

Language:

english

File:

PDF, 10.45 MB

english, 2015

22

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

Turner, Tychele N., Douville, Christopher, Kim, Dewey, Stenson, Peter D., Cooper, David N., Chakravarti, Aravinda, Karchin, Rachel

Journal:

Human Molecular Genetics

Year:

2015

Language:

english

File:

PDF, 545 KB

english, 2015

23

Comorbid symptoms of inattention, autism, and executive cognition in youth with putative genetic risk

Arnett, Anne B., Cairney, Brianna E., Wallace, Arianne S., Gerdts, Jennifer, Turner, Tychele N., Eichler, Evan E., Bernier, Raphael A.

Journal:

Journal of Child Psychology and Psychiatry

Year:

2017

Language:

english

File:

PDF, 308 KB

english, 2017

24

Genomic Patterns of De Novo Mutation in Simplex Autism

Turner, Tychele N., Coe, Bradley P., Dickel, Diane E., Hoekzema, Kendra, Nelson, Bradley J., Zody, Michael C., Kronenberg, Zev N., Hormozdiari, Fereydoun, Raja, Archana, Pennacchio, Len A., Darnell, R

Journal:

Year:

2017

Language:

english

File:

PDF, 3.60 MB

english, 2017

25

Excess of rare, inherited truncating mutations in autism

Krumm, Niklas, Turner, Tychele N, Baker, Carl, Vives, Laura, Mohajeri, Kiana, Witherspoon, Kali, Raja, Archana, Coe, Bradley P, Stessman, Holly A, He, Zong-Xiao, Leal, Suzanne M, Bernier, Raphael, Eic

Journal:

Nature Genetics

Year:

2015

Language:

english

File:

PDF, 824 KB

english, 2015

26

Large-Scale Population-Based Assessment of Psychiatric Comorbidities in Autism Spectrum Disorder and Attention-Deficit/Hyperactivity Disorder

Turner, Tychele N.

Journal:

Biological Psychiatry

Year:

2019

Language:

english

File:

PDF, 71 KB

english, 2019

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@1delivery.pm

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски