Works matching DE "LEARNING disability genetics"

Results: 28

Using Discrete Trial Training to Identify Specific Learning Impairments in Boys with Fragile X Syndrome.

Published in:

Journal of Autism & Developmental Disorders, 2014, v. 44, n. 7, p. 1659, doi. 10.1007/s10803-014-2037-6

By:

Hall, Scott;
Hustyi, Kristin;
Hammond, Jennifer;
Hirt, Melissa;
Reiss, Allan

Publication type:

Article

Specific learning disability.

Published in:

2018

By:

McDowell, Michael

Publication type:

journal article

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

Published in:

Behavior Genetics, 2011, v. 41, n. 1, p. 90, doi. 10.1007/s10519-010-9424-3

By:

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

Publication type:

Article

An Examination of Candidate Gene SNPs for Dyslexia in an Indian Sample.

Published in:

Behavior Genetics, 2011, v. 41, n. 1, p. 105, doi. 10.1007/s10519-010-9441-2

By:

Venkatesh, Shyamala K.;
Siddaiah, Anand;
Padakannaya, Prakash;
Ramachandra, Nallur B.

Publication type:

Article

SNP Variations in the 7q33 Region Containing DGKI are Associated with Dyslexia in the Finnish and German Populations.

Published in:

Behavior Genetics, 2011, v. 41, n. 1, p. 134, doi. 10.1007/s10519-010-9431-4

By:

Matsson, Hans;
Tammimies, Kristiina;
Zucchelli, Marco;
Anthoni, Heidi;
Onkamo, Päivi;
Nopola-Hemmi, Jaana;
Lyytinen, Heikki;
Leppanen, Paavo H. T.;
Neuhoff, Nina;
Warnke, Andreas;
Schulte-Körne, Gert;
Schumacher, Johannes;
Nöthen, Markus M.;
Kere, Juha;
Peyrard-Janvid, Myriam

Publication type:

Article

Moving Closer to a Public Health Model of Language and Learning Disabilities: The Role of Genetics and the Search for Etiologies.

Published in:

Behavior Genetics, 2011, v. 41, n. 1, p. 1, doi. 10.1007/s10519-010-9439-9

By:

Miller, Brett;
McCardle, Peggy

Publication type:

Article

An Application of the Elastic Net for an Endophenotype Analysis.

Published in:

Behavior Genetics, 2011, v. 41, n. 1, p. 120, doi. 10.1007/s10519-011-9443-8

By:

Palejev, Dean;
Wookyeon Hwang;
Landi, Nicole;
Eastman, Maria;
Frost, Stephen J.;
Fulbright, Robert K.;
Kidd, Judith R.;
Kidd, Kenneth K.;
Mason, Graeme F.;
Mencl, W. Einar;
Yrigollen, Carolyn;
Pugh, Kenneth R.;
Grigorenko, Elena L.

Publication type:

Article

In Search of the Perfect Phenotype: An Analysis of Linkage and Association Studies of Reading and Reading-Related Processes.

Published in:

Behavior Genetics, 2011, v. 41, n. 1, p. 6, doi. 10.1007/s10519-011-9444-7

By:

Skiba, Thomas;
Landi, Nicole;
Wagner, Richard;
Grigorenko, Elena L.

Publication type:

Article

Genome Scan for Spelling Deficits: Effects of Verbal IQ on Models of Transmission and Trait Gene Localization.

Published in:

Behavior Genetics, 2011, v. 41, n. 1, p. 31, doi. 10.1007/s10519-010-9390-9

By:

Rubenstein, Kevin;
Matsushita, Mark;
Berninger, Virginia W.;
Raskind, Wendy H.;
Wijsman, Ellen M.

Publication type:

Article

Strain Differences in Rewarded Discrimination Learning Using the Olfactory Tubing Maze.

Published in:

Behavior Genetics, 2006, v. 36, n. 6, p. 923, doi. 10.1007/s10519-006-9088-1

By:

Restivo, L.;
Chaillan, F. A.;
Ammassari-Teule, M.;
Roman, F. S.;
Marchetti, E.

Publication type:

Article

Cognitive impairment in preschool children with epilepsy.

Published in:

Epilepsia (Series 4), 2011, v. 52, n. 8, p. 1499, doi. 10.1111/j.1528-1167.2011.03092.x

By:

Rantanen, Kati;
Eriksson, Kai;
Nieminen, Pirkko

Publication type:

Article

Difference and choice: exploring prenatal testing and the use of genetic information with people with learning difficulties.

Published in:

British Journal of Learning Disabilities, 2002, v. 30, n. 2, p. 50, doi. 10.1046/j.1468-3156.2002.00164.x

By:

Ward, Linda;
Howarth, Joyce;
Rodgers, Jackie

Publication type:

Article

Genetics of developmental dyslexia.

Published in:

European Child & Adolescent Psychiatry, 2010, v. 19, n. 3, p. 179, doi. 10.1007/s00787-009-0081-0

By:

Scerri, Thomas S.;
Schulte-Körne, Gerd

Publication type:

Article

Validation of a Screening Tool for Learning Disorder in Children.

Published in:

Indian Journal of Psychological Medicine, 2017, v. 39, n. 6, p. 737, doi. 10.4103/IJPSYM.IJPSYM_29_17

By:

Vidyadharan, Varsha;
Tharayil, Harish M.;
George, Biju

Publication type:

Article

A Parent's Experience of Schooling for a Child with Prader-Willi Syndrome.

Published in:

Reach, 2009, v. 23, n. 1, p. 24

By:

Meyler, Maria

Publication type:

Article

Attention-deficit/hyperactivity disorder associated with KChIP1 rs1541665 in Kv channels accessory proteins.

Published in:

PLoS ONE, 2017, v. 12, n. 11, p. 1, doi. 10.1371/journal.pone.0188678

By:

Yuan, Fang-Fen;
Gu, Xue;
Huang, Xin;
Hou, Yu-Wei;
Zhong, Yan;
Lin, Jun;
Wu, Jing

Publication type:

Article

Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning Difficulties.

Published in:

Cytogenetic & Genome Research, 2016, v. 147, n. 2/3, p. 118, doi. 10.1159/000442583

By:

Kontodiou, Maria;
Daskalakis, Georgios;
Vetro, annalisa;
Paspaliaris, Vassilis;
Papaioannou, Georgios;
Dagklis, Themistoklis;
Tsakiridis, Ioannis;
Ziegler, Monika;
Liehr, Thomas;
Thomaidis, Loretta;
Papoulidis, Ioannis;
Manolakos, Emmanouil

Publication type:

Article

A study of developmental speech and language disorders in twins.

Published in:

Journal of Speech & Hearing Research, 1992, v. 35, n. 5, p. 1086, doi. 10.1044/jshr.3505.1086

By:

Lewis, Barbara A.;
Thompson, Lee A.

Publication type:

Article

Characterization of two familial cases presenting with a syndromic specific learning disorder and carrying (17q;21q) unbalanced translocations.

Published in:

Clinical Case Reports, 2018, v. 6, n. 5, p. 827, doi. 10.1002/ccr3.1450

By:

Coton, Julie;
Labalme, Audrey;
Till, Marianne;
Bussy, Gerald;
Krifi Papoz, Sonia;
Lesca, Gaetan;
Heron, Delphine;
Sanlaville, Damien;
Edery, Patrick;
des Portes, Vincent;
Rossi, Massimiliano

Publication type:

Article

The cognitive profiles of Jordanian students at risk for math disability.

Published in:

International Journal of Inclusive Education, 2018, v. 22, n. 10, p. 1093, doi. 10.1080/13603116.2017.1415382

By:

Abu-Hamour, Bashir

Publication type:

Article

Gestational age and learning disabilities.

Published in:

Developmental Medicine & Child Neurology, 2015, v. 57, n. 5, p. 401, doi. 10.1111/dmcn.12681

By:

Alloway, Tracy Packiam;
Horton, John

Publication type:

Article

Mechanism for the learning deficits in a mouse model of neurofibromatosis type 1.

Published in:

Nature, 2002, v. 415, n. 6871, p. 526, doi. 10.1038/nature711

By:

Costa, Rui M.;
Federov, Nikolai B.;
Kogan, Jeff H.;
Murphy, Geoffrey G.;
Stern, Joel;
Ohno, Masuo;
Kucherlapati, Raju;
Jacks, Tyler;
Silva, Alcino J.

Publication type:

Article

Genetic Influences on Learning Disabilities and Speech and Language Disorders.

Published in:

Child Development, 1983, v. 54, n. 2, p. 369, doi. 10.2307/1129698

By:

Pennington, Bruce F.;
Smith, Shelley D.

Publication type:

Article

Should We Undertake Genetic Research on Intelligence?

Published in:

Bioethics, 1999, v. 13, n. 3/4, doi. 10.1111/1467-8519.00161

By:

Newson, Ainsley;
Williamson, Robert

Publication type:

Article

Reading and Writing Skills in Children With Specific Learning Disabilities With and Without Developmental Coordination Disorder.

Published in:

2018

By:

Di Brina, Carlo;
Rampoldi, Paola;
Rossetti, Serena;
Penge, Roberta;
Averna, Roberto

Publication type:

journal article

Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism.

Published in:

Clinical Genetics, 2011, v. 79, n. 1, p. 79, doi. 10.1111/j.1399-0004.2010.01590.x

By:

Filges, I.;
Röthlisberger, B.;
Blattner, A.;
Boesch, N.;
Demougin, P.;
Wenzel, F.;
Huber, A. R.;
Heinimann, K.;
Weber, P.;
Miny, P.

Publication type:

Article

Examining MTSS Implementation Across Systems for SLD Identification: A Case Study.

Published in:

2018

By:

Barrett, Courtenay A.;
Newman, Daniel S.

Publication type:

Case Study

Characterizing the ADHD phenotype for genetic studies.

Published in:

Developmental Science, 2005, v. 8, n. 2, p. 115, doi. 10.1111/j.1467-7687.2005.00398.x

By:

Stevenson, Jim;
Asherson, Phil;
Hay, David;
Levy, Florence;
Swanson, Jim;
Thapar, Anita;
Willcutt, Erik

Publication type:

Article