Physician

Psychiatry

Pablo V. Gejman practices Psychiatry. Pablo Gejman is a published doctor as well. He has 101 publications published. The latest was: The sensitivity of denaturing gradient gel electrophoresis: a blinded analysis.

Publications

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• Genetic studies of body mass index yield new insights for obesity biology.
• A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder.
• Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia.
• Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
• Transcriptome study of differential expression in schizophrenia.
• Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent.
• Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia.
• Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
• Implication of a rare deletion at distal 16p11.2 in schizophrenia.
• Genome-wide survey of interindividual differences of RNA stability in human lymphoblastoid cell lines.
• Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.
• Genetics of Schizophrenia: New Findings and Challenges.
• Genomewide Association Analysis of Symptoms of Alcohol Dependence in the Molecular Genetics of Schizophrenia (MGS2) Control Sample.
• Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications.
• Erratum: Common variants in P2RY11 are associated with narcolepsy.
• Common variants in P2RY11 are associated with narcolepsy.
• Genome-wide approaches to schizophrenia.
• The Internet-based MGS2 control sample: self report of mental illness.
• The role of genetics in the etiology of schizophrenia.
• Narcolepsy is strongly associated with the T-cell receptor alpha locus.
• No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric genetics.
• Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in ...
• Polymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia.
• No major schizophrenia locus detected on chromosome 1q in a large multicenter sample.
• A sequence variant in human KALRN impairs protein function and coincides with reduced cortical thickness.
• Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain.
• Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q.
• Functional analysis of the human D5 dopamine receptor missense and nonsense variants: differences in dopamine binding affinities.
• Chromosomes 19 and 20 report.
• Analysis of neuroleptic binding affinities and potencies for the different human D2 dopamine receptor missense variants.
• The sensitivity of denaturing gradient gel electrophoresis: a blinded analysis.
• A novel mutation adjacent to the switch III domain of G(S alpha) in a patient with pseudohypoparathyroidism.
• Ernst Rüdin and Nazi euthanasia: another stain on his career.
• Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees.
• Antagonist binding characteristics of the Ser311-->Cys variant of human dopamine D2 receptor in vivo and in vitro.
• No abnormality in the gene for the G protein stimulatory alpha subunit in patients with bipolar disorder.
• Analysis of DRPLA trinucleotide repeats in schizophrenia.
• Functional analysis of the human D2 dopamine receptor missense variants.
• No association detected between a D3 receptor gene-expressed variant and schizophrenia.
• The thyrotropin receptor (TSH-R) is not an oncogene for thyroid tumors: structural studies of the TSH-R and the alpha-subunit of Gs in human thyroid neoplasms.
• Linkage analysis of fifty-seven microsatellite loci to bipolar disorder.
• No structural mutation in the dopamine D2 receptor gene in alcoholism or schizophrenia. Analysis using denaturing gradient gel electrophoresis.
• Nonsense mutations in the C-terminal SH2 region of the GTPase activating protein (GAP) gene in human tumours.
• Genetic analysis of the catalytic domain of the GAP gene in human lung cancer cell lines.
• Mutational analysis of candidate genes in psychiatric disorders.
• Allelic variation in the D4 dopamine receptor (DRD4) gene does not predict response to clozapine.
• Detection of mutations and polymorphisms of Gs alpha subunit gene by denaturing gradient gel electrophoresis.
• Normal structural dopamine type 2 receptor gene in prolactin-secreting and other pituitary tumors.
• Changes in drinking behavior caused by superior cervical ganglionectomy and pinealectomy in rats.
• The sympathetic superior cervical ganglia as peripheral neuroendocrine centers.
• Further evidence of adrenergic control of translocation and intracellular levels of estrogen receptors in rat pineal gland.
• Hormone effects on muscarinic cholinergic binding in bovine and rat sympathetic superior cervical ganglia.
• The sympathetic superior cervical ganglia as "little neuroendocrine brains".
• Norepinephrine stimulates testosterone aromatization and inhibits 5 alpha reduction via beta-adrenoceptors in rat pineal gland.
• Circadian rhythm and neural regulation of rat pineal angiotensin converting enzyme.
• The effects of field inversion electrophoresis on small DNA fragment mobility and its relevance to DNA polymorphism research.
• X-chromosome markers and manic-depressive illness. Rejection of linkage to Xq28 in nine bipolar pedigrees.
• Genetic mapping of common diseases: the challenges of manic-depressive illness and schizophrenia.
• Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis.
• Manic depressive illness not linked to factor IX region in an independent series of pedigrees.
• Activating mutations of the stimulatory G protein in the McCune-Albright syndrome.
• Genetic mapping of the Gs-alpha subunit gene (GNAS1) to the distal long arm of chromosome 20 using a polymorphism detected by denaturing gradient gel electrophoresis.
• Sequence tagged site (STS) TaqI RFLP at dopamine beta-hydroxylase (DBH).
• Detection of mutations in insulin receptor gene by denaturing gradient gel electrophoresis.
• Hypertrophic cardiomyopathy: failure to demonstrate mutations in exon 13 of the cardiac beta myosin heavy-chain gene.
• A heterozygous 4-bp deletion mutation in the Gs alpha gene (GNAS1) in a patient with Albright hereditary osteodystrophy.
• Allelic loss from chromosome 11 in parathyroid tumors.
• Response to Mitchell and Porteus.
• Neurotransmitter-controlled steroid hormone receptors in the central nervous system.
• GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia.
• Genome-wide association study of recurrent early-onset major depressive disorder.
• Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies.
• Meta-analysis of 32 genome-wide linkage studies of schizophrenia.
• Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms.
• Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2.
• Complexities in psychiatric genetics.
• Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia.
• Linkage analysis of schizophrenia to chromosome 15.
• Multicenter linkage study of schizophrenia loci on chromosome 22q.
• Polymorphisms in the 5''-untranslated region of the human serotonin receptor 1B (HTR1B) gene affect gene expression.
• Influential ideas and experimental progress in schizophrenia genetics research.
• Genetic diversity of the human serotonin receptor 1B (HTR1B) gene.
• Major corrections are indicated for ''Comparative proteome analysis of the hippocampus implicates chromosome 6q in schizophrenia''.
• Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III.
• Update on chromosomal locations for psychiatric disorders: report of the interim meeting of chromosome workshop chairpersons from the VIIth World Congress of Psychiatr...
• History of the eugenic movement.
• Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor.
• DNA variation and psychopharmacology of the human serotonin receptor 1B (HTR1B) gene.
• Linkage disequilibrium for schizophrenia at the chromosome 15q13-14 locus of the alpha7-nicotinic acetylcholine receptor subunit gene (CHRNA7).
• Identification of loci associated with schizophrenia by genome-wide association and follow-up.
• Genomewide association studies: history, rationale, and prospects for psychiatric disorders.
• New models of collaboration in genome-wide association studies: the Genetic Association Information Network.
• DTNBP1 (Dystrobrevin binding protein 1) and schizophrenia: association evidence in the 3' end of the gene.
• Common variants on chromosome 6p22.1 are associated with schizophrenia.
• Genetic risk sum score comprised of common polygenic variation is associated with body mass index.
• Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.
• Hundreds of variants clustered in genomic loci and biological pathways affect human height.
• Neuregulin 1 (NRG1 ) and schizophrenia: analysis of a US family sample and the evidence in the balance.
• Genome-wide association study identifies five new schizophrenia loci.
• ACSL6 Is Associated with the Number of Cigarettes Smoked and Its Expression Is Altered by Chronic Nicotine Exposure.

Schools

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• Universidad De Buenos Aires Facultad De Ciencias Medicas

Doctors Specialties

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• Psychiatry

Accepted Insurances

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Education

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• National Institutes of Health Clinical Center
• University of Buenos Aires

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