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1.
Disruption of the neurexin 1 gene is associated with schizophrenia.
Hum Mol Genet;
18(5): 988-96, 2009 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18945720
2.
Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma.
Blood;
132(19): 2040-2052, 2018 Nov 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30194254
3.
Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes.
Hum Genomics;
13(1): 37, 2019 08 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-31429796
4.
Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders.
Mol Psychiatry;
2019 Nov 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31712721
5.
Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression.
Mol Psychiatry;
2019 Nov 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31712720
6.
Pathway-Specific Genetic Risk for Alzheimer's Disease Differentiates Regional Patterns of Cortical Atrophy in Older Adults.
Cereb Cortex;
2019 Aug 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31402375
7.
Protein-coding variants contribute to the risk of atopic dermatitis and skin-specific gene expression.
J Allergy Clin Immunol;
2019 Nov 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31707051
8.
A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis.
Hum Mol Genet;
26(13): 2577-2588, 2017 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28449029
9.
Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing.
Mol Psychiatry;
2018 Aug 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-30116028
10.
Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.
Mutagenesis;
2019 Oct 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31586183
11.
No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsy.
Epilepsia;
60(5): e31-e36, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30719712
12.
Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes.
Int J Cancer;
143(11): 2800-2813, 2018 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29987844
13.
Influence of obesity-related risk factors in the aetiology of glioma.
Br J Cancer;
118(7): 1020-1027, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29531326
14.
Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture.
Am J Hum Genet;
97(6): 816-36, 2015 Dec 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26626624
15.
Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study.
Mol Med;
24(1): 30, 2018 06 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30134812
16.
Impact of atopy on risk of glioma: a Mendelian randomisation study.
BMC Med;
16(1): 42, 2018 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29540232
17.
The severity of human peri-implantitis lesions correlates with the level of submucosal microbial dysbiosis.
J Clin Periodontol;
2018 Oct 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-30341964
18.
BMP Inhibition in Seminomas Initiates Acquisition of Pluripotency via NODAL Signaling Resulting in Reprogramming to an Embryonal Carcinoma.
PLoS Genet;
11(7): e1005415, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26226633
19.
Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study.
Lancet;
387(10023): 1085-1093, 2016 Mar 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-26806518
20.
Genomewide association study on monoclonal gammopathy of unknown significance (MGUS).
Eur J Haematol;
99(1): 70-79, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28375557