المؤلفون: Gruen, DeMille Mm, Jan C. Frijters, Elizabeth G. Atkinson, Truong Dt, Andrew K. Adams, Joan Bosson-Heenan, Guertin El

مصطلحات موضوعية: Minor allele frequency, Genetics, Candidate gene, Reading disability, Expression quantitative trait loci, Dyslexia, medicine, Single-nucleotide polymorphism, Genome-wide association study, Biology, Allele, medicine.disease

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::2e2bd4aeef7a466a5a7bd1f172bf290b
https://doi.org/10.1101/2021.01.05.423827

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المؤلفون: Cutforth T; Department of Neurology, Columbia University Medical Center, 650 West 168 Street, Room 310E, New York, NY 10032, USA., DeMille MM; Department of Pediatrics, Yale Child Health Research Center, Yale University School of Medicine, 464 Congress Avenue, Suite S208, New Haven, CT 06519, USA., Agalliu I; Department of Epidemiology & Population Health, Albert Einstein College of Medicine, 1300 Morris Park Ave., Room 1315-B, Bronx, NY 10461, USA., Agalliu D; Department of Neurology, Columbia University Medical Center, 650 West 168 Street, Room 310E, New York, NY 10032, USA; Departments of Pathology & Cell Biology & Pharmacology, Columbia University Medical Center, 650 West 168 Street, Room 310E, New York, NY 10032, USA.

المصدر: Future neurology [Future Neurol] 2016 Dec; Vol. 11 (1), pp. 63-76.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Future Medicine Ltd Country of Publication: England NLM ID: 101278119 Publication Model: Print Cited Medium: Print ISSN: 1479-6708 (Print) Linking ISSN: 14796708 NLM ISO Abbreviation: Future Neurol Subsets: PubMed not MEDLINE

المؤلفون: Truong DT; Department of Pediatrics, Yale School of Medicine, New Haven, CT, 06510, USA., Shriberg LD; Waisman Center, University of Wisconsin-Madison, Madison, WI, 53705, USA., Smith SD; Department of Pediatrics, University of Nebraska at Omaha, Omaha, NE, 68182, USA., Chapman KL; Department of Communication Sciences and Disorders, University of Utah, Salt Lake City, UT, 84112, USA., Scheer-Cohen AR; Department of Speech-Language Pathology, California State University, San Marcos, CA, 92096, USA., DeMille MM; Department of Pediatrics, Yale School of Medicine, New Haven, CT, 06510, USA., Adams AK; Department of Genetics, Yale School of Medicine, New Haven, CT, 06510, USA., Nato AQ; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, 98195, USA., Wijsman EM; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, 98195, USA.; Department of Biostatistics and Department of Genome Sciences, University of Washington, Seattle, WA, 98195, USA., Eicher JD; Department of Genetics, Yale School of Medicine, New Haven, CT, 06510, USA., Gruen JR; Department of Pediatrics, Yale School of Medicine, New Haven, CT, 06510, USA. jeffrey.gruen@yale.edu.; Department of Genetics, Yale School of Medicine, New Haven, CT, 06510, USA. jeffrey.gruen@yale.edu.; Investigative Medicine Program, Yale School of Medicine, New Haven, CT, 06510, USA. jeffrey.gruen@yale.edu.

المصدر: Human genetics [Hum Genet] 2016 Dec; Vol. 135 (12), pp. 1329-1341. Date of Electronic Publication: 2016 Aug 17.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE

مواضيع طبية MeSH: Dyslexia/*genetics , Language Disorders/*genetics , Quantitative Trait Loci/*genetics , Speech Disorders/*genetics, Adolescent ; Adult ; Aged ; Aged, 80 and over ; Child ; Child, Preschool ; Chromosome Mapping ; Chromosomes, Human, Pair 13/genetics ; Drosophila Proteins ; Dyslexia/physiopathology ; Female ; Genetic Linkage ; Genetic Predisposition to Disease ; Genotype ; Humans ; Language Disorders/physiopathology ; Lod Score ; Male ; Membrane Proteins ; Middle Aged ; Nuclear Proteins ; Pedigree ; Reading ; Speech Disorders/physiopathology ; Writing

المؤلفون: Palmatier MA; Department of Genetics, Yale University School of Medicine, New Haven, CT 06520-8005, USA., Pakstis AJ, Speed W, Paschou P, Goldman D, Odunsi A, Okonofua F, Kajuna S, Karoma N, Kungulilo S, Grigorenko E, Zhukova OV, Bonne-Tamir B, Lu RB, Parnas J, Kidd JR, DeMille MM, Kidd KK

المصدر: Molecular psychiatry [Mol Psychiatry] 2004 Sep; Vol. 9 (9), pp. 859-70.

نوع المنشور: Journal Article; Research Support, U.S. Gov't, P.H.S.

بيانات الدورية: Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print Cited Medium: Print ISSN: 1359-4184 (Print) Linking ISSN: 13594184 NLM ISO Abbreviation: Mol Psychiatry Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Predisposition to Disease* , Genetic Variation* , Promoter Regions, Genetic*, Catechol O-Methyltransferase/*genetics , Schizophrenia/*genetics, Databases, Genetic ; Gene Frequency ; Haplotypes ; Humans ; Linkage Disequilibrium

المؤلفون: DeMille MM; Department of Genetics, Yale University School of Medicine, New Haven, CT 06520-8005, USA., Kidd JR, Ruggeri V, Palmatier MA, Goldman D, Odunsi A, Okonofua F, Grigorenko E, Schulz LO, Bonne-Tamir B, Lu RB, Parnas J, Pakstis AJ, Kidd KK

المصدر: Human genetics [Hum Genet] 2002 Dec; Vol. 111 (6), pp. 521-37. Date of Electronic Publication: 2002 Oct 01.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.

بيانات الدورية: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0340-6717 (Print) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Variation* , Linkage Disequilibrium* , Promoter Regions, Genetic*, Catechol O-Methyltransferase/*genetics, Base Sequence ; DNA Primers ; Haplotypes ; Humans

المؤلفون: DeMille MM; Howard Hughes Medical Institute, Department of Molecular and Cell Biology University of California, Berkeley 94720, USA., Kimmel BE, Rubin GM

المصدر: Gene [Gene] 1996 Dec 12; Vol. 183 (1-2), pp. 103-8.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.

بيانات الدورية: Publisher: Elsevier/North-Holland Country of Publication: Netherlands NLM ID: 7706761 Publication Model: Print Cited Medium: Print ISSN: 0378-1119 (Print) Linking ISSN: 03781119 NLM ISO Abbreviation: Gene Subsets: MEDLINE

مواضيع طبية MeSH: Cell Cycle Proteins* , Drosophila Proteins* , Gene Expression Regulation, Developmental* , Microtubule-Associated Proteins*, DNA-Binding Proteins/*physiology , Drosophila melanogaster/*genetics , Photoreceptor Cells, Invertebrate/*growth & development , Transcription Factors/*physiology, Amino Acid Sequence ; Animals ; Base Sequence ; Cell Adhesion Molecules/genetics ; DNA, Complementary/genetics ; DNA-Binding Proteins/genetics ; Drosophila melanogaster/growth & development ; Enhancer Elements, Genetic/genetics ; Genes, Insect/genetics ; Microfilament Proteins ; Molecular Sequence Data ; Open Reading Frames/genetics ; Phosphoproteins/genetics ; Restriction Mapping ; Sequence Analysis, DNA ; Sequence Homology, Amino Acid ; Signal Transduction/genetics ; Transcription Factors/genetics ; Zinc Fingers/genetics