Detalles de la búsqueda
1.
Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases.
Immunity;
42(6): 1185-96, 2015 Jun 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-26084028
2.
Druggable genome in attention deficit/hyperactivity disorder and its co-morbid conditions. New avenues for treatment.
Mol Psychiatry;
26(8): 4004-4015, 2021 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-31628418
3.
Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing.
Mol Psychiatry;
25(9): 2047-2057, 2020 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-30116028
4.
The (Broad-Sense) Genetic Correlations Among Four Measures of Inattention and Hyperactivity in 12 Year Olds.
Behav Genet;
50(4): 273-288, 2020 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-32529491
5.
A candidate gene investigation of methylphenidate response in adult attention-deficit/hyperactivity disorder patients: results from a naturalistic study.
J Neural Transm (Vienna);
123(8): 859-65, 2016 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-27091191
6.
Genome-wide analyses of aggressiveness in attention-deficit hyperactivity disorder.
Am J Med Genet B Neuropsychiatr Genet;
171(5): 733-47, 2016 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-27021288
7.
Expanding the toolbox of ADHD genetics. How can we make sense of parent of origin effects in ADHD and related behavioral phenotypes?
Behav Brain Funct;
11(1): 33, 2015 Oct 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-26475699
8.
Epistatic and gene wide effects in YWHA and aromatic amino hydroxylase genes across ADHD and other common neuropsychiatric disorders: Association with YWHAE.
Am J Med Genet B Neuropsychiatr Genet;
168(6): 423-432, 2015 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-26172220
9.
COL11A1 is associated with developmental dysplasia of the hip and secondary osteoarthritis in the HUNT study.
Osteoarthr Cartil Open;
6(1): 100424, 2024 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-38283578
10.
Maternal Fiber Intake During Pregnancy and Development of Attention-Deficit/Hyperactivity Disorder Symptoms Across Childhood: The Norwegian Mother, Father, and Child Cohort Study.
Biol Psychiatry;
95(9): 839-848, 2024 May 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-38142720
11.
A variant in LIN28B is associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure.
Am J Hum Genet;
86(4): 519-25, 2010 Apr 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-20303062
12.
HTRA2 p.G399S in Parkinson disease, essential tremor, and tremulous cervical dystonia.
Proc Natl Acad Sci U S A;
112(18): E2268, 2015 May 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-25825781
13.
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains.
Nat Genet;
55(2): 198-208, 2023 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-36702997
14.
An international collaborative family-based whole genome quantitative trait linkage scan for myopic refractive error.
Mol Vis;
18: 720-9, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-22509102
15.
Assessing the contribution of genetic nurture to refractive error.
Eur J Hum Genet;
30(11): 1226-1232, 2022 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-35618892
16.
Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder.
Nat Genet;
54(8): 1117-1124, 2022 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-35927488
17.
Investigating Shared Genetic Basis Across Tourette Syndrome and Comorbid Neurodevelopmental Disorders Along the Impulsivity-Compulsivity Spectrum.
Biol Psychiatry;
90(5): 317-327, 2021 09 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33714545
18.
Genetic association study of childhood aggression across raters, instruments, and age.
Transl Psychiatry;
11(1): 413, 2021 07 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-34330890
19.
Shared genetic background between children and adults with attention deficit/hyperactivity disorder.
Neuropsychopharmacology;
45(10): 1617-1626, 2020 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-32279069
20.
Myocilin polymorphisms and high myopia in subjects of European origin.
Mol Vis;
15: 213-22, 2009.
Artículo
en Inglés
| MEDLINE | ID: mdl-19180258