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Confirming genes influencing risk to cleft lip with/without cleft palate in a case–parent trio study

Human genetics, 2013-07, Vol.132 (7), p.771-781

2013

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Meta-analysis of two genome-wide association studies of bipolar disorder reveals important points of agreement

Molecular psychiatry, 2008-05, Vol.13 (5), p.466-467

2008

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Effects of a genome-wide supported psychosis risk variant on neural activation during a theory-of-mind task

Molecular psychiatry, 2011-04, Vol.16 (4), p.462-470

2011

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A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

Molecular psychiatry, 2008-02, Vol.13 (2), p.197-207

2008

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First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children

Molecular psychiatry, 2011-01, Vol.16 (1), p.97-107

2011

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Association between the insulin-induced gene 2 ( ) and weight gain in a German sample of antipsychotic-treated schizophrenic patients: perturbation of SREBP-controlled lipogenesis in drug-related metabolic adverse effects?

Molecular psychiatry, 2009-03, Vol.14 (3), p.308-317

2009

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Genetic factors influencing the risk of multiple myeloma bone disease

Leukemia, 2016-04, Vol.30 (4), p.883-888

2016

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Genetic prediction of male pattern baldness

PLoS genetics, 2017-02, Vol.13 (2), p.e1006594

2017

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Increased Activity of Coagulation Factor XII (Hageman Factor) Causes Hereditary Angioedema Type III

American journal of human genetics, 2006-12, Vol.79 (6), p.1098-1104

2006

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Epistatic interaction of genetic depression risk variants in the human subgenual cingulate cortex during memory encoding

Translational psychiatry, 2014-03, Vol.4 (3), p.e372-e372

2014

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Defective glycosylation of coagulation factor XII underlies hereditary angioedema type III

The Journal of clinical investigation, 2015-08, Vol.125 (8), p.3132-3146

2015

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Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples

Molecular psychiatry, 2010-05, Vol.15 (5), p.463-472

2010

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Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature

American journal of human genetics, 2011-06, Vol.88 (6), p.788-795

2011

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USO DE INTELIGÊNCIA ARTIFICAL NO DIAGNÓSTICO DE LEUCEMIA MIELOIDE AGUDA: REVISÃO E ANÁLISE CRÍTICA DA LITERATURA

Hematology, Transfusion and Cell Therapy, 2024-10, Vol.46, p.S378-S379

2024

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G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth

Nature genetics, 2008-03, Vol.40 (3), p.329-334

2008

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Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

Nature genetics, 2010-01, Vol.42 (1), p.24-26

2010

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PORFIRIA CUTÂNEA TARDA COMO DIAGNÓSTICO DIFERENCIAL DE LESÕES CUTÂNEAS: UM RELATO DE CASO

Hematology, Transfusion and Cell Therapy, 2024-10, Vol.46, p.S8-S9

2024

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SÍNDROME MIELODISPLÁSICA EM ADULTOS JOVENS: REVISÃO E ANÁLISE CRÍTICA DA LITERATURA

Hematology, Transfusion and Cell Therapy, 2024-10, Vol.46, p.S452-S452

2024

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Genetic variation in schizophrenia-risk-gene dysbindin 1 modulates brain activation in anterior cingulate cortex and right temporal gyrus during language production in healthy individuals

NeuroImage (Orlando, Fla.), 2009-10, Vol.47 (4), p.2016-2022

2009

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Variability of 5-HT2C receptor cys23ser polymorphism among European populations and vulnerability to affective disorder

Molecular psychiatry, 2001-09, Vol.6 (5), p.579-585

2001

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Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts

Genetics (Austin), 2014-07, Vol.197 (3), p.1039-1044

2014

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MANIFESTAÇÃO ATÍPICA DE DOENÇA MIELOPROLIFERATIVA TRANSITÓRIA EM PACIENTE COM SÍNDROME DE DOWN: UM RELATO DE CASO

Hematology, Transfusion and Cell Therapy, 2024-10, Vol.46, p.S1137-S1137

2024

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Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1

Nature genetics, 2010-02, Vol.42 (2), p.128-131

2010

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Association of the DTNBP1 genotype with cognition and personality traits in healthy subjects

Psychological medicine, 2009-10, Vol.39 (10), p.1657-1665

2009

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Confirming genes influencing risk to cleft lip with/without cleft palate in a case–parent trio study

Meta-analysis of two genome-wide association studies of bipolar disorder reveals important points of agreement

Effects of a genome-wide supported psychosis risk variant on neural activation during a theory-of-mind task

A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children

Association between the insulin-induced gene 2 ( ) and weight gain in a German sample of antipsychotic-treated schizophrenic patients: perturbation of SREBP-controlled lipogenesis in drug-related metabolic adverse effects?

Genetic factors influencing the risk of multiple myeloma bone disease

Genetic prediction of male pattern baldness

Increased Activity of Coagulation Factor XII (Hageman Factor) Causes Hereditary Angioedema Type III

Epistatic interaction of genetic depression risk variants in the human subgenual cingulate cortex during memory encoding

Defective glycosylation of coagulation factor XII underlies hereditary angioedema type III

Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples

Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature

USO DE INTELIGÊNCIA ARTIFICAL NO DIAGNÓSTICO DE LEUCEMIA MIELOIDE AGUDA: REVISÃO E ANÁLISE CRÍTICA DA LITERATURA

G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth

Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24

PORFIRIA CUTÂNEA TARDA COMO DIAGNÓSTICO DIFERENCIAL DE LESÕES CUTÂNEAS: UM RELATO DE CASO

SÍNDROME MIELODISPLÁSICA EM ADULTOS JOVENS: REVISÃO E ANÁLISE CRÍTICA DA LITERATURA

Genetic variation in schizophrenia-risk-gene dysbindin 1 modulates brain activation in anterior cingulate cortex and right temporal gyrus during language production in healthy individuals

Variability of 5-HT2C receptor cys23ser polymorphism among European populations and vulnerability to affective disorder

Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts

MANIFESTAÇÃO ATÍPICA DE DOENÇA MIELOPROLIFERATIVA TRANSITÓRIA EM PACIENTE COM SÍNDROME DE DOWN: UM RELATO DE CASO

Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1

Association of the DTNBP1 genotype with cognition and personality traits in healthy subjects

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