(Q34060360)

English

Incorporation of molecular data and redefinition of phenotype: new approaches to genetic epidemiology of bipolar manic depressive illness and schizophrenia.

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22034205%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Incorporation of molecular data and redefinition of phenotype: new approaches to genetic epidemiology of bipolar manic depressive illness and schizophrenia (English)

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22034205%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

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author name string

E S Gershon

1

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Europe PubMed Central

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15 January 2020

J A Badner

2

1 reference

Europe PubMed Central

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15 January 2020

publication date

1 March 2001

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Europe PubMed Central

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15 January 2020

Dialogues in Clinical Neuroscience

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22034205%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

3

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22034205%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

1

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22034205%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

63-71

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22034205%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Advancing paternal age and the risk of schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Attention, memory, and motor skills as childhood predictors of schizophrenia-related psychoses: the New York High-Risk Project.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

The NOTCH4 locus is associated with susceptibility to schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

The unstable trinucleotide repeat story of major psychosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Genetics of psychiatric disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: a common expansion locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Susceptibility loci for bipolar disorder: overlap with inherited vulnerability to schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Bipolar illness and schizophrenia as oligogenic diseases: implications for the future

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Full-genome scan for linkage in 50 families segregating the bipolar affective disease phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

A rare coding variant within the wolframin gene in bipolar and unipolar affective disorder cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Anticipation in schizophrenia: a review and reconsideration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Trinucleotide repeat expansion and neuropsychiatric disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Cognitive and behavioral precursors of schizophrenia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Do schizophrenia and affective disorder share susceptibility genes?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Linkage of a composite inhibitory phenotype to a chromosome 22q locus in eight Utah families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Candidate-gene association studies of schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Neurobehavioral deficits at adolescence in children at risk for schizophrenia: The Jerusalem Infant Development Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Increased expression of Wnt-1 in schizophrenic brains

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Alternative phenotypes for the complex genetics of schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Neuropsychological functioning among the nonpsychotic relatives of schizophrenic patients: a 4-year follow-up study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Further evidence for the increased power of LOD scores compared with nonparametric methods

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

A decrease of reelin expression as a putative vulnerability factor in schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Failure to demonstrate parent-of-origin effect in transmission of bipolar II disorder.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

A genome-wide search for schizophrenia susceptibility genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Comprehensive human genetic maps: individual and sex-specific variation in recombination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

A large sample of finnish diabetic sib-pairs reveals no evidence for a non-insulin-dependent diabetes mellitus susceptibility locus at 2qter

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Genome scan of European-American schizophrenia pedigrees: results of the NIMH Genetics Initiative and Millennium Consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

NIMH Genetics Initiative Millenium Schizophrenia Consortium: linkage analysis of African-American pedigrees

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Closing in on genes for manic-depressive illness and schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Meta-analysis of linkage data under worst-case conditions: a demonstration using the human OB region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Allele-sharing models: LOD scores and accurate linkage tests

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 4, 7, 9, 18, 19, 20, and 21q.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

NCAM and schizophrenia: genetic studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Genetic anticipation and imprinting in bipolar I illness.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

A complete genome screen for genes predisposing to severe bipolar disorder in two Costa Rican pedigrees.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Age at onset in schizophrenia and risk of illness in relatives. Results from the Roscommon Family Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Parametric and nonparametric linkage analysis: a unified multipoint approach

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

A manic depressive history.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Evidence for linkage of bipolar disorder to chromosome 18 with a parent-of-origin effect

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

A genome-wide search for genes predisposing to manic-depression, assuming autosomal dominant inheritance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Gaussian models for genetic linkage analysis using complete high-resolution maps of identity by descent

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Patterns of maternal transmission in bipolar affective disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Genes with triplet repeats: candidate mediators of neuropsychiatric disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Linkage strategies for genetically complex traits. I. Multilocus models

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Reduction in temporal lobe size in siblings with schizophrenia: a magnetic resonance imaging study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Gene expression in mental illness: a navigation chart to future progress

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Behavioral markers of schizophrenia useful for genetic studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

5 July 2018

Bipolar disorder and variation at a common polymorphism (A1832G) within exon 8 of the Wolfram gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

28 October 2018

Clinical features of schizophrenia and linkage to chromosomes 5q, 6p, 8p, and 10p in the Irish Study of High-Density Schizophrenia Families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

28 October 2018

Homicidal behavior in schizophrenia associated with a genetic polymorphism determining low catechol O-methyltransferase (COMT) activity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

28 October 2018

Suggestive linkage of chromosome 10p to schizophrenia is not due to transmission ratio distortion.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

28 October 2018

Age at onset anticipation in familial schizophrenia. Does the phenomenon even exist?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

28 October 2018

Direct power comparisons between simple LOD scores and NPL scores for linkage analysis in complex diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

28 October 2018

Neurologic signs of cerebellar and cortical sensory dysfunction in schizophrenics and their relatives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

28 October 2018

Age at onset and outcome in schizophrenia are related to the degree of familial loading.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

28 October 2018

The power to detect linkage in complex disease by means of simple LOD-score analyses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

28 October 2018

Large CAG/CTG repeats are associated with childhood-onset schizophrenia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

28 October 2018

Lateral ventricular enlargement in schizophrenic probands and their siblings with schizophrenia-related disorders.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

28 October 2018

Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees: chromosomes 2, 11, 13, 14, and X.

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

28 October 2018

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

9 December 2018

Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 1, 6, 8, 10, and 12.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

28 October 2018

A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

28 October 2018

Mitochondrial DNA Sequence Diversity in Bipolar Affective Disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

28 October 2018

Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

28 October 2018

A locus for bipolar affective disorder on chromosome 4p

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3181639

28 October 2018

P300, a state and a trait marker in schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome scan of schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association study of a functional catechol-O-methyltransferase gene polymorphism in Japanese schizophrenics

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosome search for schizophrenia susceptibility genes in multiply affected families

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An international two–stage genome–wide search for schizophrenia susceptibility genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of bipolar disorder with the 5178 polymorphism in mitochondrial DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family characteristics of deficit and nondeficit schizophrenia in the Roscommon Family Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide search for linkage of bipolar affective disorders in a very large pedigree derived from a homogeneous population in quebec points to a locus of major effect on chromosome 12q23-q24

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anticipation in schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Family Study of Schizoaffective, Bipolar I, Bipolar II, Unipolar, and Normal Control Probands

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Systematic mutation analysis of the catechol O-methyltransferase gene as a candidate gene for schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Velocardiofacial manifestations and microdeletions in schizophrenic inpatients

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib–pair linkage analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of evidence for association between the COMT locus and schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family-based association studies of bipolar disorder with candidate genes involved in dopamine neurotransmission: DBH, DAT1, COMT, DRD2, DRD3 and DRD5

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping NIDDM Susceptibility Loci in French Families: Studies With Markers in the Region of NIDDM1 on Chromosome 2q

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meta-analysis by combining p-values: simulated linkage studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic scan for genes predisposing to schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural Brain Abnormalities in Patients With Schizophrenia and Their Healthy Siblings

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mode of inheritance in families of patients with lithium-responsive affective disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal inheritance and chromosome 18 allele sharing in unilineal bipolar illness pedigrees

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progress in a genome scan for linkage in schizophrenia in a large Swedish kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parent-of-origin effect in transmission of bipolar disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Short CAG repeats within the hSKCa3 gene associated with schizophrenia: results of a family-based study

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adequacy of single-locus approximations for linkage analyses of oligogenic traits: extension to multigenerational pedigree structures

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage disequilibrium on the COMT gene in French schizophrenics and controls

1 reference

https://pubmed.ncbi.nlm.nih.gov/22034205

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22034205%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22034205%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

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