Detalhe da pesquisa
1.
Using neuroimaging genomics to investigate the evolution of human brain structure.
Proc Natl Acad Sci U S A
; 119(40): e2200638119, 2022 10 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36161899
2.
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.
Proc Natl Acad Sci U S A
; 119(35): e2202764119, 2022 08 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-35998220
3.
Self-reported impact of developmental stuttering across the lifespan.
Dev Med Child Neurol
; 64(10): 1297-1306, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35307825
4.
A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development.
Mol Psychiatry
; 24(7): 1065-1078, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29463886
5.
Epigenetic DNA methylation changes associated with headache chronification: A retrospective case-control study.
Cephalalgia
; 38(2): 312-322, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28103696
6.
Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas.
Hum Genet
; 135(4): 425-439, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26899160
7.
Involvement of astrocyte and oligodendrocyte gene sets in migraine.
Cephalalgia
; 36(7): 640-7, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26646788
8.
Gene-based pleiotropy across migraine with aura and migraine without aura patient groups.
Cephalalgia
; 36(7): 648-57, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26660531
9.
Gene-expression and in vitro function of mesenchymal stromal cells are affected in juvenile myelomonocytic leukemia.
Haematologica
; 100(11): 1434-41, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26294732
10.
RNA expression profiling in brains of familial hemiplegic migraine type 1 knock-in mice.
Cephalalgia
; 34(3): 174-82, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23985897
11.
The Association Between Stuttering Burden and Psychosocial Aspects of Life in Adults.
J Speech Lang Hear Res
; 67(5): 1385-1399, 2024 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38625147
12.
Genome-Wide Analyses of Vocabulary Size in Infancy and Toddlerhood: Associations With Attention-Deficit/Hyperactivity Disorder, Literacy, and Cognition-Related Traits.
Biol Psychiatry
; 95(9): 859-869, 2024 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38070845
13.
Beyond the Global Brain Differences: Intraindividual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers.
Biol Psychiatry
; 95(2): 147-160, 2024 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37661008
14.
Epigenetic mechanisms in migraine: a promising avenue?
BMC Med
; 11: 26, 2013 Feb 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-23379668
15.
Pearls and pitfalls in genetic studies of migraine.
Cephalalgia
; 33(8): 614-25, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23671257
16.
The shared genetic architecture and evolution of human language and musical rhythm.
bioRxiv
; 2023 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37961248
17.
Self-Reported Stuttering Severity Is Accurate: Informing Methods for Large-Scale Data Collection in Stuttering.
J Speech Lang Hear Res
; : 1-10, 2023 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38052068
18.
Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities.
Transl Psychiatry
; 12(1): 495, 2022 11 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-36446759
19.
Genome-wide association study of musical beat synchronization demonstrates high polygenicity.
Nat Hum Behav
; 6(9): 1292-1309, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35710621
20.
Discovery of 42 genome-wide significant loci associated with dyslexia.
Nat Genet
; 54(11): 1621-1629, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36266505