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2. Evidence for major gene transmission of developmental dyslexia. Pennington BF; Gilger JW; Pauls D; Smith SA; Smith SD; DeFries JC JAMA; 1991 Sep; 266(11):1527-34. PubMed ID: 1880884 [TBL] [Abstract][Full Text] [Related]
3. Parental contributions to longitudinal stability of cognitive measures in the Colorado Family Reading Study. DeFries JC; Baker LA Child Dev; 1983 Apr; 54(2):388-95. PubMed ID: 6872630 [TBL] [Abstract][Full Text] [Related]
4. Commingling and segregation analysis of reading performance in families of normal reading probands. Gilger JW; Borecki IB; DeFries JC; Pennington BF Behav Genet; 1994 Jul; 24(4):345-55. PubMed ID: 7993313 [TBL] [Abstract][Full Text] [Related]
5. Cognitive ability profiles in families of reading-disabled children. Decker SN; DeFries JC Dev Med Child Neurol; 1981 Apr; 23(2):217-27. PubMed ID: 7215709 [TBL] [Abstract][Full Text] [Related]
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7. Gender ratios among reading-disabled children and their siblings as a function of parental impairment. Wadsworth SJ; DeFries JC; Stevenson J; Gilger JW; Pennington BF J Child Psychol Psychiatry; 1992 Oct; 33(7):1229-39. PubMed ID: 1400704 [TBL] [Abstract][Full Text] [Related]
8. High risk of reading disability and speech sound disorder in rolandic epilepsy families: case-control study. Clarke T; Strug LJ; Murphy PL; Bali B; Carvalho J; Foster S; Tremont G; Gagnon BR; Dorta N; Pal DK Epilepsia; 2007 Dec; 48(12):2258-65. PubMed ID: 17850323 [TBL] [Abstract][Full Text] [Related]
9. Risk factors for reading disability in families with rolandic epilepsy. Vega YH; Smith A; Cockerill H; Tang S; Agirre-Arrizubieta Z; Goyal S; Pina M; Akman CI; Jolleff N; McGinnity C; Gomez K; Gupta R; Hughes E; Jackman J; McCormick D; Oren C; Scott D; Taylor J; Trounce J; Clarke T; Kugler S; Mandelbaum DE; McGoldrick P; Wolf S; Strug LJ; Pal DK Epilepsy Behav; 2015 Dec; 53():174-9. PubMed ID: 26580214 [TBL] [Abstract][Full Text] [Related]
10. The genetics of specific reading disability. Finucci JM; Guthrie JT; Childs AL; Abbey H; Childs B Ann Hum Genet; 1976 Jul; 40(1):1-23. PubMed ID: 962317 [TBL] [Abstract][Full Text] [Related]
11. The Colorado Longitudinal Twin Study of Reading Difficulties and ADHD: Etiologies of Comorbidity and Stability. Wadsworth SJ; DeFries JC; Willcutt EG; Pennington BF; Olson RK Twin Res Hum Genet; 2015 Dec; 18(6):755-61. PubMed ID: 26537134 [TBL] [Abstract][Full Text] [Related]
12. Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects. Loo SK; Fisher SE; Francks C; Ogdie MN; MacPhie IL; Yang M; McCracken JT; McGough JJ; Nelson SF; Monaco AP; Smalley SL Mol Psychiatry; 2004 May; 9(5):485-93. PubMed ID: 14625563 [TBL] [Abstract][Full Text] [Related]
13. Reading disability, immune disorders and non-right-handedness: twin and family studies of their relations. Gilger JW; Pennington BF; Green P; Smith SM; Smith SD Neuropsychologia; 1992 Mar; 30(3):209-27. PubMed ID: 1574158 [TBL] [Abstract][Full Text] [Related]
14. Cognitive and familial risk evidence converged: A data-driven identification of distinct and homogeneous subtypes within the heterogeneous sample of reading disabled children. Willems G; Jansma B; Blomert L; Vaessen A Res Dev Disabil; 2016; 53-54():213-31. PubMed ID: 26922163 [TBL] [Abstract][Full Text] [Related]
15. Psychiatric comorbidity in children and adolescents with reading disability. Willcutt EG; Pennington BF J Child Psychol Psychiatry; 2000 Nov; 41(8):1039-48. PubMed ID: 11099120 [TBL] [Abstract][Full Text] [Related]
16. Language development, literacy skills, and predictive connections to reading in Finnish children with and without familial risk for dyslexia. Torppa M; Lyytinen P; Erskine J; Eklund K; Lyytinen H J Learn Disabil; 2010; 43(4):308-21. PubMed ID: 20479461 [TBL] [Abstract][Full Text] [Related]
17. Twin study of the etiology of comorbidity between reading disability and attention-deficit/hyperactivity disorder. Willcutt EG; Pennington BF; DeFries JC Am J Med Genet; 2000 Jun; 96(3):293-301. PubMed ID: 10898903 [TBL] [Abstract][Full Text] [Related]
18. Family patterns of developmental dyslexia, part II: behavioral phenotypes. Wolff PH; Melngailis I; Obregon M; Bedrosian M Am J Med Genet; 1995 Dec; 60(6):494-505. PubMed ID: 8825885 [TBL] [Abstract][Full Text] [Related]
19. Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses. Deffenbacher KE; Kenyon JB; Hoover DM; Olson RK; Pennington BF; DeFries JC; Smith SD Hum Genet; 2004 Jul; 115(2):128-38. PubMed ID: 15138886 [TBL] [Abstract][Full Text] [Related]
20. Association of the dopamine receptor D1 gene, DRD1, with inattention symptoms in families selected for reading problems. Luca P; Laurin N; Misener VL; Wigg KG; Anderson B; Cate-Carter T; Tannock R; Humphries T; Lovett MW; Barr CL Mol Psychiatry; 2007 Aug; 12(8):776-85. PubMed ID: 17310237 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]