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Select item 105774771.

A novel homozygous splice variant in DNAAF4 is associated with asthenozoospermia : DNAAF4 is associated with asthenozoospermia

Xiaobin Zhu, Chen Chen, Jian Song, Shijue Dong, Xuhui Zeng, Zhihong Niu, Yanwei Sha, Xiaoning Zhang

Acta Biochim Biophys Sin (Shanghai) 2023 Oct 25; 55(10): 1689–1692. Published online 2023 Sep 7. doi: 10.3724/abbs.2023147

PMCID:: PMC10577477

Article PDF–878K

Select item 76468672.

Novel dynein axonemal assembly factor 1 mutations identified using whole-exome sequencing in patients with primary ciliary dyskinesia

Lei Zhou, Zhuozhe Li, Chunling Du, Cuicui Chen, Yingxin Sun, Liang Gu, Feng Zhou, Yuanlin Song

Mol Med Rep. 2020 Dec; 22(6): 4707–4715. Published online 2020 Oct 6. doi: 10.3892/mmr.2020.11562

PMCID:: PMC7646867

Abstract Article PDF–643K

Select item 53819643.

A Family-Based Association Analysis and Meta-Analysis of the Reading Disabilities Candidate Gene DYX1C1

C. Tran, F. Gagnon, K.G. Wigg, Y. Feng, L. Gomez, T.D. Cate-Carter, E.N. Kerr, L.L. Field, B.J. Kaplan, M.W. Lovett, C.L. Barr

Am J Med Genet B Neuropsychiatr Genet. Author manuscript; available in PMC 2017 Apr 5.

Published in final edited form as: Am J Med Genet B Neuropsychiatr Genet. 2013 Mar; 162B(2): 146–156. Published online 2013 Jan 22. doi: 10.1002/ajmg.b.32123

PMCID:: PMC5381964

Abstract Article PDF–751K

Select item 34416034.

Association of the DYX1C1 Dyslexia Susceptibility Gene with Orthography in the Chinese Population

Yuping Zhang, Jun Li, Twila Tardif, Margit Burmeister, Sandra M. Villafuerte, Catherine McBride-Chang, Hong Li, Bingjie Shi, Weilan Liang, Zhixiang Zhang, Hua Shu

PLoS One. 2012; 7(9): e42969. Published online 2012 Sep 13. doi: 10.1371/journal.pone.0042969

PMCID:: PMC3441603

Abstract Article PDF–258K

Select item 33372515.

aThe dyslexia candidate gene DYX1C1 is a potential marker of poor survival in breast cancer

Gustaf Rosin, Ulf Hannelius, Linda Lindström, Per Hall, Jonas Bergh, Johan Hartman, Juha Kere

BMC Cancer. 2012; 12: 79. Published online 2012 Feb 29. doi: 10.1186/1471-2407-12-79

PMCID:: PMC3337251

Abstract Article PDF–1.0M

Select item 31231826.

Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children

Cadmon KP Lim, Connie SH Ho, Crystal HN Chou, Mary MY Waye

Behav Brain Funct. 2011; 7: 16. Published online 2011 May 20. doi: 10.1186/1744-9081-7-16

PMCID:: PMC3123182

Abstract Article PDF–324K

Select item 54171427.

The rs3743205 SNP Is Important for the Regulation of the Dyslexia Candidate Gene DYX1C1 by Estrogen Receptor β and DNA Methylation

Kristiina Tammimies, Isabel Tapia-Páez, Joëlle Rüegg, Gustaf Rosin, Juha Kere, Jan-Åke Gustafsson, Ivan Nalvarte

Mol Endocrinol. April 1, 2012; 26(4): 619–629. Published online 2012 Mar 1. doi: 10.1210/me.2011-1376

PMCID:: PMC5417142

Abstract Article

Select item 48334938.

Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region

K. G. Wigg, Y. Feng, J. Crosbie, R. Tannock, J. L. Kennedy, A. Ickowicz, M. Malone, R. Schachar, C. L. Barr

Genes Brain Behav. Author manuscript; available in PMC 2016 Apr 15.

Published in final edited form as: Genes Brain Behav. 2008 Nov; 7(8): 877–886. doi: 10.1111/j.1601-183X.2008.00425.x

PMCID:: PMC4833493

Abstract Article PDF–495K

Select item 39396769.

Pleiotropic Effects of DCDC2 and DYX1C1 Genes on Language and Mathematics Traits in Nuclear Families of Developmental Dyslexia

Cecilia Marino, Sara Mascheretti, Valentina Riva, Francesca Cattaneo, Catia Rigoletto, Marianna Rusconi, Jeffrey R. Gruen, Roberto Giorda, Claudio Lazazzera, Massimo Molteni

Behav Genet. Author manuscript; available in PMC 2014 Mar 3.

Published in final edited form as: Behav Genet. 2011 Jan; 41(1): 67–76. Published online 2010 Nov 3. doi: 10.1007/s10519-010-9412-7

PMCID:: PMC3939676

Abstract Article PDF–65K

Select item 302967710.

Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects

D. F. Newbury, S. Paracchini, T. S. Scerri, L. Winchester, L. Addis, Alex J. Richardson, J. Walter, J. F. Stein, J. B. Talcott, A. P. Monaco

Behav Genet. 2011; 41(1): 90–104. Published online 2010 Dec 17. doi: 10.1007/s10519-010-9424-3

PMCID:: PMC3029677

Abstract Article PDF–282K

Select item 173561911.

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK

T Scerri, S Fisher, C Francks, I MacPhie, S Paracchini, A Richardson, J Stein, A Monaco

J Med Genet. 2004 Nov; 41(11): 853–857. doi: 10.1136/jmg.2004.018341

PMCID:: PMC1735619

Summary PDF–120K

Select item 1101488812.

Developmental dyslexia susceptibility genes DNAAF4, DCDC2, and NRSN1 are associated with brain function in fluently reading adolescents and young adults

Nea Rinne, Patrik Wikman, Elisa Sahari, Juha Salmi, Elisabet Einarsdóttir, Juha Kere, Kimmo Alho

Cereb Cortex. 2024 Apr; 34(4): bhae144. Published online 2024 Apr 12. doi: 10.1093/cercor/bhae144

PMCID:: PMC11014888

Abstract Article PDF–1.2M

Select item 502470113.

Ciliary dyslexia candidate genes DYX1C1 and DCDC2 are regulated by Regulatory Factor X (RFX) transcription factors through X-box promoter motifs

Kristiina Tammimies, Andrea Bieder, Gilbert Lauter, Debora Sugiaman-Trapman, Rachel Torchet, Marie-Estelle Hokkanen, Jan Burghoorn, Eero Castrén, Juha Kere, Isabel Tapia-Páez, Peter Swoboda

FASEB J. 2016 Oct; 30(10): 3578–3587. Published online 2016 Jul 22. doi: 10.1096/fj.201500124RR

PMCID:: PMC5024701

Abstract Article

Select item 522309414.

Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm Defects

Tamara Paff, Niki T. Loges, Isabella Aprea, Kaman Wu, Zeineb Bakey, Eric G. Haarman, Johannes M.A. Daniels, Erik A. Sistermans, Natalija Bogunovic, Gerard W. Dougherty, Inga M. Höben, Jörg Große-Onnebrink, Anja Matter, Heike Olbrich, Claudius Werner, Gerard Pals, Miriam Schmidts, Heymut Omran, Dimitra Micha

Am J Hum Genet. 2017 Jan 5; 100(1): 160–168. Published online 2016 Dec 29. doi: 10.1016/j.ajhg.2016.11.019

PMCID:: PMC5223094

Abstract Article PDF–1.9M

Select item 249345715.

The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia

Isabel Tapia-Páez, Kristiina Tammimies, Satu Massinen, Ananda L. Roy, Juha Kere

FASEB J. 2008 Aug; 22(8): 3001–3009. doi: 10.1096/fj.07-104455

PMCID:: PMC2493457

Abstract Article

Select item 20879616.

A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain

Mikko Taipale, Nina Kaminen, Jaana Nopola-Hemmi, Tuomas Haltia, Birgitta Myllyluoma, Heikki Lyytinen, Kurt Muller, Minna Kaaranen, Perttu J. Lindsberg, Katariina Hannula-Jouppi, Juha Kere

Proc Natl Acad Sci U S A. 2003 Sep 30; 100(20): 11553–11558. Published online 2003 Sep 3. doi: 10.1073/pnas.1833911100

PMCID:: PMC208796

Abstract Article PDF–439K

Select item 333842117.

Exploring the Transcriptome of Ciliated Cells Using In Silico Dissection of Human Tissues

Alexander E. Ivliev, Peter A. C. 't Hoen, Willeke M. C. van Roon-Mom, Dorien J. M. Peters, Marina G. Sergeeva

PLoS One. 2012; 7(4): e35618. Published online 2012 Apr 25. doi: 10.1371/journal.pone.0035618

PMCID:: PMC3338421

Abstract Article PDF–4.3M

Select item 308450018.

Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population

S Paracchini, Q W Ang, F J Stanley, A P Monaco, C E Pennell, A J O Whitehouse

Genes Brain Behav. 2011 Mar; 10(2): 158–165. doi: 10.1111/j.1601-183X.2010.00651.x

PMCID:: PMC3084500

Abstract Article PDF–584K

Select item 589505119.

ZMYND10 stabilizes intermediate chain proteins in the cytoplasmic pre-assembly of dynein arms

Kyeong Jee Cho, Shin Hye Noh, Soo Min Han, Won-Il Choi, Hye-Youn Kim, Seyoung Yu, Joon Suk Lee, John Hoon Rim, Min Goo Lee, Friedhelm Hildebrandt, Heon Yung Gee

PLoS Genet. 2018 Mar; 14(3): e1007316. Published online 2018 Mar 30. doi: 10.1371/journal.pgen.1007316

PMCID:: PMC5895051

Abstract Article PDF–20M

Select item 400044420.

DYX1C1 is required for axonemal dynein assembly and ciliary motility

Aarti Tarkar, Niki T. Loges, Christopher E. Slagle, Richard Francis, Gerard W. Dougherty, Joel V. Tamayo, Brett Shook, Marie Cantino, Daniel Schwartz, Charlotte Jahnke, Heike Olbrich, Claudius Werner, Johanna Raidt, Petra Pennekamp, Marouan Abouhamed, Rim Hjeij, Gabriele Köhler, Matthias Griese, You Li, Kristi Lemke, Nikolas Klena, Xiaoqin Liu, George Gabriel, Kimimasa Tobita, Martine Jaspers, Lucy C. Morgan, Adam J. Shapiro, Stef J.F. Letteboer, Dorus A. Mans, Johnny L. Carson, Margaret W. Leigh, Whitney E. Wolf, Serafine Chen, Jane S. Lucas, Alexandros Onoufriadis, Vincent Plagnol, Miriam Schmidts, Karsten Boldt, UK10K, Ronald Roepman, Maimoona Zariwala, Cecilia W. Lo, Hannah M. Mitchison, Michael R. Knowles, Rebecca D. Burdine, Joseph J. LoTurco, Heymut Omran

Nat Genet. Author manuscript; available in PMC 2014 Apr 26.

Published in final edited form as: Nat Genet. 2013 Sep; 45(9): 995–1003. Published online 2013 Jul 21. doi: 10.1038/ng.2707

PMCID:: PMC4000444

Abstract Article PDF–2.1M

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