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Lista de obras de Ian W. Craig

A 19 bp deletion polymorphism adjacent to a dinucleotide repeat polymorphism at the human dopamine beta-hydroxylase locus

artículo científico publicado en 1992

A 2-Mb YAC contig encompassing three loci (DXF34, DXS14, and DXS390) that lie between Xp11.2 translocation breakpoints associated with incontinentia pigmenti type 1.

artículo científico publicado en 1994

A behavioural genomic analysis of DNA markers associated with general cognitive ability in 7-year-olds

artículo científico publicado en 2005

A bidirectional YAC walk from the Norrie disease (NDP) locus

artículo científico publicado en 1995

A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays

artículo científico publicado en 2005

A comparison of the fine structure and nucleic acid biochemistry of chloroplasts and blue-green algae

artículo científico publicado en 1971

A dinucleotide repeat polymorphism at the DMD locus

artículo científico publicado en 1991

A direct light effect on maintaining photosynthetic activity of Nitella chloroplasts

artículo científico publicado en 1970

A dopamine transporter gene functional variant associated with cocaine abuse in a Brazilian sample.

artículo científico publicado en 2006

A follow-up case-control association study of tractable (druggable) genes in recurrent major depression

artículo científico publicado en 2011

A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder

artículo científico publicado en 2015

A genome wide association study of mathematical ability reveals an association at chromosome 3q29, a locus associated with autism and learning difficulties: a preliminary study

artículo científico publicado en 2014

A genome-wide association study of social and non-social autistic-like traits in the general population using pooled DNA, 500 K SNP microarrays and both community and diagnosed autism replication samples

artículo científico publicado en 2009

A genome-wide scan of 1842 DNA markers for allelic associations with general cognitive ability: a five-stage design using DNA pooling and extreme selected groups

artículo científico publicado en 2001

A genome-wide significant linkage for severe depression on chromosome 3: the depression network study

artículo científico publicado en 2011

A highly informative X-chromosome probe, M27 beta, can be used for the determination of tumour clonality

artículo científico publicado en 1990

A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosome

artículo científico publicado en 1990

A longitudinal study of epigenetic variation in twins

artículo científico publicado en 2010

A longitudinal twin study of skewed X chromosome-inactivation

artículo científico publicado en 2011

A mega-analysis of genome-wide association studies for major depressive disorder

artículo científico publicado en 2012

A model incorporating potential skewed X-inactivation in MZ girls suggests that X-linked QTLs exist for several social behaviours including autism spectrum disorder

artículo científico publicado en 2008

A novel expression based approach for assessing the inactivation status of human X-linked genes

artículo científico publicado en 2000

A preliminary analysis of the segregation of human hydroxyacyl coenzyme A dehydrogenase in human-mouse somatic cell hybrids

artículo científico publicado en 1976

A procedure for the analysis of citrate synthase (E.C. 4.1.3.7) in somatic cell hybrids ⬇️

artículo científico publicado el 1 de agosto de 1973

ATP-binding cassette sub-family F member 1 (ABCF1) is identified as a putative therapeutic target of escitalopram in the inflammatory cytokine pathway

artículo científico publicado en 2013

AVPR1A and SLC6A4 polymorphisms in choral singers and non-musicians: a gene association study

artículo científico publicado en 2012

Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia

article

Allele association studies with SSR and SNP markers at known physical distances within a 1 Mb region embracing the ALDH2 locus in the Japanese, demonstrates linkage disequilibrium extending up to 400 kb

artículo científico publicado en 2000

Altered ribosomal RNA genes in mitochondria from mammalian cells with chloramphenicol resistance

artículo científico publicado en 1981

An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5' end of the monoamine oxidase A gene

artículo científico publicado en 1992

An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5′ end of the Monoamine Oxidase A gene

article

Analysis of Proteins Synthesized in Mitochondria of Cultured Mammalian Cells. An Assessment of Current Approaches and Problems in Interpretation

artículo científico publicado en 1976

Analysis of X-chromosome inactivation and presumptive expression of the Wiskott-Aldrich syndrome (WAS) gene in hematopoietic cell lineages of a thrombocytopenic carrier female of WAS.

artículo científico publicado en 1991

Analysis of the 5' regulatory region of the human Norrie's disease gene: evidence that a non-translated CT dinucleotide repeat in exon one has a role in controlling expression

artículo científico publicado en 1999

Analysis of the monoamine oxidase genes and the Norrie disease gene locus in narcolepsy

artículo científico publicado en 1999

Antidepressant-dependent mRNA changes in mouse associated with hippocampal neurogenesis in a mouse model of depression

artículo científico publicado en 2012

Application of microarrays to the analysis of the inactivation status of human X-linked genes expressed in lymphocytes

article

Assessing individual differences in genome-wide gene expression in human whole blood: reliability over four hours and stability over 10 months

artículo científico publicado en 2009

Assignment of a gene for tryptophanyl-transfer ribonucleic acid synthetase (E.C. 6.1.1.2) to human chromosome 14

article

Assignment of a gene for tryptophanyl-transfer ribonucleic acid synthetase to human chromosome 14

article

Assignment of the genes for human beta-glucuronidase and mitochondrial malate dehydrogenase to the region pter leads to q22 of chromosome 7.

artículo científico publicado en 1977

Assignment of the haemophilia B (factor IX) locus to the q26-qter region of the X chromosome

artículo científico publicado en 1984

Assignment of the human tyrosine hydroxylase gene to chromosome 11.

artículo científico publicado en 1984

Association analysis of DAOA and DAO in bipolar disorder: results from two independent case-control studies

article

Association analysis of MAOA and COMT with neuroticism assessed by peers

artículo científico publicado en 2003

Association analysis of mild mental impairment using DNA pooling to screen 432 brain-expressed single-nucleotide polymorphisms.

artículo científico publicado en 2005

Association analysis of monoamine genes with measures of depression and anxiety in a selected community sample of siblings

artículo científico publicado en 2005

Association of DISC1 and TSNAX genes and affective disorders in the depression case-control (DeCC) and bipolar affective case-control (BACCS) studies

artículo científico publicado en 2009

Association of the dystrobrevin binding protein 1 gene (DTNBP1) in a bipolar case-control study (BACCS)

article

Association of the serotonin transporter gene, neuroticism and smoking behaviours

artículo científico publicado en 2008

Biochemical and immunological studies of the monoamine-oxidizing activities of cultured human cells

artículo científico publicado el 1 de enero de 1977

Biosynthesis of proteins involved with photosynthetic activity in enucleated acetabularia sp ⬇️

artículo científico publicado el 15 de octubre de 1970

Bipolar disorder susceptibility region on chromosome 3q29 not confirmed in a case–control association study

artículo científico publicado en 2011

Brain monoamine oxidase A activity predicts trait aggression

artículo científico publicado en 2008

C-phycocyanin and allophycocyanin in two species of blue-green algae

artículo científico publicado en 1968

CGM2, a member of the carcinoembryonic antigen gene family is down-regulated in colorectal carcinomas

artículo científico publicado en 1994

CYP2C19 genotype predicts steady state escitalopram concentration in GENDEP.

artículo científico publicado en 2011

Candidate Genes Expression Profile Associated with Antidepressants Response in the GENDEP Study: Differentiating between Baseline ‘Predictors' and Longitudinal ‘Targets'.

artículo científico publicado en 2012

Candidate genes expression profile associated with antidepressants response in the GENDEP study: differentiating between baseline 'predictors' and longitudinal 'targets'.

artículo científico publicado en 2012

Carrier detection in X-linked retinitis pigmentosa by multipoint DNA analysis. Problems due to genetic heterogeneity

artículo científico publicado en 1991

Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.

artículo científico publicado en 1997

Characterization and mapping of the mouse NDP (Norrie disease) locus (Ndp).

artículo científico publicado en 1996

Characterization of a YAC containing part or all of the Norrie disease locus

artículo científico publicado en 1992

Characterization of a highly polymorphic region near the first exon of the human MAOA gene containing a GT dinucleotide and a novel VNTR motif

article

Characterization of a mutation within the NDP gene in a family with a manifesting female carrier

artículo científico publicado en 1993

Characterization of novel promoter and enhancer elements of the mouse homologue of the Dent disease gene, CLCN5, implicated in X-linked hereditary nephrolithiasis

artículo científico publicado en 1999

Characterization of the genomic organization of human carcinoembryonic antigen (CEA): comparison with other family members and sequence analysis of 5' controlling region

artículo científico publicado en 1990

Chasing behaviour genes into the next millennium

artículo científico publicado en 2000

Chloroplast development in charophyceae

artículo científico publicado en 1971

Cloning of mouse mitochondrial DNA in E. coli affects bacterial viability

artículo científico publicado en 1980

Construction of two YAC contigs in human Xp11.23-p11.22, one encompassing the loci OATL1, GATA, TFE3, and SYP, the other linking DXS255 to DXS146.

artículo científico publicado en 1995

Convergent animal and human evidence suggests a role of PPM1A gene in response to antidepressants

artículo científico publicado en 2010

Copy number variants and therapeutic response to antidepressant medication in major depressive disorder

artículo científico publicado en 2014

Cytoplasmic transfer of a determinant for chloramphenicol resistance between mammalian cell lines

artículo científico publicado en 1978

DETECTING MATERNAL CELL CONTAMINATION IN PRENATAL DIAGNOSIS

artículo científico publicado en 1989

DNA Pooling: a tool for large-scale association studies

artículo científico publicado en 2002

DNA analysis and recombination in X-linked retinitis pigmentosa

scientific article published on 01 January 1990

DNA by mail: an inexpensive and noninvasive method for collecting DNA samples from widely dispersed populations

artículo científico publicado en 1997

DNA from buccal swabs recruited by mail: evaluation of storage effects on long-term stability and suitability for multiplex polymerase chain reaction genotyping

artículo científico publicado en 2003

DNA pooling analysis of 21 norepinephrine transporter gene SNPs with attention deficit hyperactivity disorder: no evidence for association

artículo científico publicado en 2005

DNA pooling and dense marker maps: a systematic search for genes for cognitive ability

artículo científico publicado en 1999

DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children

artículo científico publicado en 1999

Depression Case Control (DeCC) Study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorder.

artículo científico publicado en 2009

Depressive disorder moderates the effect of the FTO gene on body mass index

article

Differences in the mitochondrially synthesized subunits of human and mouse cytochrome c oxidase

artículo científico publicado en 1977

Differences in the products of mitochondrial protein synthesis in vivo in Human and mouse cells and their potential use as markers for the mitochondrial genome in human--mouse somatic cell hybrids

artículo científico publicado en 1974

Differential methylation of the X-chromosome is a possible source of discordance for bipolar disorder female monozygotic twins

artículo científico publicado en 2008

Dinucleotide repeat polymorphism at the MAOA locus

artículo científico publicado en 1991

Dinucleotide repeat polymorphism at the human dopamine beta-hydroxylase (DBH) locus

artículo científico publicado en 1992

Dinucleotide repeat polymorphism in CEA gene

artículo científico publicado en 1991

Dinucleotide repeat polymorphism in CEA gene

article

Dissecting the genetic heterogeneity of depression through age at onset

artículo científico publicado en 2012

Effect of cytochrome CYP2C19 metabolizing activity on antidepressant response and side effects: Meta-analysis of data from genome-wide association studies

Engineering in Genomics [variable number tandem repeats as agents of functional regulation in the genome]

scientific article published on 01 March 2008

Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants.

artículo científico publicado en 2012

Epigenomic and transcriptomic signatures of a Klinefelter syndrome (47,XXY) karyotype in the brain

artículo científico publicado en 2014

Erratum: The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

article

Estimating the heritability of reporting stressful life events captured by common genetic variants

artículo científico publicado en 2012

Evidence for monozygotic twin (MZ) discordance in methylation level at two CpG sites in the promoter region of the catechol-O-methyltransferase (COMT) gene

artículo científico publicado en 2006

Evidence that brain MAO A activity does not correspond to MAO A genotype in healthy male subjects

artículo científico publicado en 2006

Evidence that in X-linked immunodeficiency with hyperimmunoglobulinemia M the intrinsic immunoglobulin heavy chain class switch mechanism is intact

scientific article published on 01 December 1990

Expression of the dopamine transporter gene is regulated by the 3' UTR VNTR: Evidence from brain and lymphocytes using quantitative RT-PCR.

artículo científico publicado en 2002

Familiality and SNP heritability of age at onset and episodicity in major depressive disorder

artículo científico publicado en 2015

Functional effects of a tandem duplication polymorphism in the 5'flanking region of the DRD4 gene

artículo científico publicado en 2004

Functional genetic polymorphisms in serotonin and dopamine gene systems and their significance in behavioural disorders

scientific article published on January 2008

Functional polymorphisms in dopamine and serotonin pathway genes

artículo científico publicado en 2006

GENESiS: creating a composite index of the vulnerability to anxiety and depression in a community-based sample of siblings

artículo científico publicado en 2000

Gene-environment interaction analysis of serotonin system markers with adolescent depression

artículo científico publicado en 2004

Genes within the serotonergic system are differentially expressed in human brain

artículo científico publicado en 2009

Genetic Control of Mitochondrial Enzymes in Human–Mouse Somatic Cell Hybrids

artículo científico publicado en 1973

Genetic differences in cytochrome P450 enzymes and antidepressant treatment response

artículo científico publicado en 2013

Genetic predictors of increase in suicidal ideation during antidepressant treatment in the GENDEP project.

artículo científico publicado en 2009

Genetic predictors of response to antidepressants in the GENDEP project

artículo científico publicado en 2009

Genetic predictors of response to serotonergic and noradrenergic antidepressants in major depressive disorder: a genome-wide analysis of individual-level data and a meta-analysis

artículo científico publicado en 2012

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study

artículo científico publicado en 2014

Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders

artículo científico publicado en 2013

Genetics of Criminal and Antisocial Behaviour.

artículo científico publicado en 1996

Genetics of human aggressive behaviour

artículo científico publicado en 2009

Genetics, environment and cognitive abilities: review and work in progress towards a genome scan for quantitative trait locus associations using DNA pooling.

artículo científico publicado en 2001

Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium

artículo científico publicado en 2016

Genome-wide association analysis of copy number variation in recurrent depressive disorder.

artículo científico publicado en 2011

Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder

artículo científico publicado en 2011

Genome-wide association study of bipolar disorder in European American and African American individuals

artículo científico publicado en 2009

Genome-wide association study of co-occurring anxiety in major depression

artículo científico publicado en 2013

Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project

artículo científico publicado en 2010

Genome-wide association study of major recurrent depression in the U.K. population

artículo científico publicado en 2010

Genome-wide linkage analysis of a composite index of neuroticism and mood-related scales in extreme selected sibships

artículo científico publicado en 2004

Genome-wide pharmacogenetics of antidepressant response in the GENDEP project

artículo científico publicado en 2010

Genome-wide quantitative trait locus association scan of general cognitive ability using pooled DNA and 500K single nucleotide polymorphism microarrays.

artículo científico publicado en 2008

Genomewide association scan of suicidal thoughts and behaviour in major depression

artículo científico publicado en 2011

Genomic Odyssey

artículo científico publicado en 1994

Genomic Organization of Human Centromeric Alpha Satellite DNA: Characterization of a Chromosome 17 Alpha Satellite Sequence

artículo científico publicado en 1987

Genotyping DNA pools on microarrays: tackling the QTL problem of large samples and large numbers of SNPs

artículo científico publicado en 2005

Genotyping pooled DNA on microarrays: a systematic genome screen of thousands of SNPs in large samples to detect QTLs for complex traits.

artículo científico publicado en 2004

High-Throughput Single-Nucleotide Polymorphism Genotyping by Fluorescent Competitive Allele-Specific Polymerase Chain Reaction (SNiPTag)

artículo científico publicado en 2002

Homologous expressed genes in the human sex chromosome pairing region

artículo científico publicado en 1985

Human behavioural genetics of cognitive abilities and disabilities ⬇️

artículo científico publicado el 1 de diciembre de 1997

Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins.

artículo científico publicado en 2014

Identification of incomplete coding sequences for steroid sulphatase on the human Y chromosome: evidence for an ancestral pseudoautosomal gene?

artículo científico publicado en 1987

Immunological studies of human monoamine oxidases

artículo científico publicado en 1982

Infant zygosity can be assigned by parental report questionnaire data

artículo científico publicado en 2000

Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene

artículo científico publicado en 2003

Integrative mouse and human mRNA studies using WGCNA nominates novel candidate genes involved in the pathogenesis of major depressive disorder.

artículo científico publicado en 2013

Interaction between serotonin transporter gene variants and life events predicts response to antidepressants in the GENDEP project.

artículo científico publicado en 2010

Interaction between specific forms of childhood maltreatment and the serotonin transporter gene (5-HTT) in recurrent depressive disorder

artículo científico publicado en 2012

Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individuals

artículo científico publicado en 2017

Interspecific variation in products of animal mitochondrial protein synthesis

artículo científico publicado en 1976

Introductory guide to the language of molecular genetics

artículo científico publicado en 2005

Investigating the genetic variation underlying episodicity in major depressive disorder: suggestive evidence for a bipolar contribution

artículo científico publicado en 2013

Isolation and characterization of a candidate gene for Norrie disease

artículo científico publicado en 1992

Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22.

artículo científico publicado en 1989

Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis

artículo científico publicado en 1987

Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome

Isolation and detailed characterization of human cell lines resistant to d-threo-chloramphenicol

artículo científico publicado en 1976

Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis).

artículo científico publicado en 1994

LACK OF AN ASSOCIATION BETWEEN TESTICULAR CANCERS AND LOW STEROID SULPHATASE ACTIVITY IN PERIPHERAL LEUCOCYTES

artículo científico publicado en 1985

Language-impaired children: No sign of the FOXP2 mutation.

artículo científico publicado en 2002

Leber's hereditary optic neuropathy: implications of the sex ratio for linkage studies in families with the 3460 ND1 mutation.

artículo científico publicado en 1995

Letter: Mitochondria, autoimmunity, and oncogenesis

artículo científico publicado en 1975

Linkage of X-linked retinitis pigmentosa to the hypervariable DNA marker M27? (DXS255)

scientific article published on 01 February 1989

Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11

artículo científico publicado en 1988

Localisation of Y chromosome sequences in normal and 'XX' males

artículo científico publicado en 1987

Localization of human liver 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase (PFKFB1) within a YAC contig in Xp11.21.

artículo científico publicado en 1997

Localization of human monoamine oxidase-A gene to Xp11.23-11.4 by in situ hybridization: Implications for norrie disease

article

Localization of the X inactivation centre on the human X chromosome in Xq13.

artículo científico publicado en 1991

Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22–Xp11.3

article

Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa

artículo científico publicado en 1990

Long-range chromosomal mapping of the carcinoembryonic antigen (CEA) gene family cluster

artículo científico publicado en 1992

Long-range organization of reiterated sequences, including the SSX1 cDNA at the OATL1 cluster in Xp11.23.

artículo científico publicado en 1995

Long-range physical mapping around the human steroid sulfatase locus

artículo científico publicado en 1990

MAOA, maltreatment, and gene–environment interaction predicting children's mental health: new evidence and a meta-analysis

artículo científico publicado en 2006

Mapping of 12 translocation breakpoints in the Xp21 region with respect to the locus for Duchenne muscular dystrophy

scientific article published on 01 January 1988

Mapping of X chromosome translocation breakpoints in females with Duchenne muscular dystrophy with respect to exons of the dystrophin gene

article

Mapping of Xp21 translocation breakpoints in and around the DMD gene by pulsed field gel electrophoresis

article

Mapping of the Menkes locus to Xq13.3 distal to the X-inactivation center by an intrachromosomal insertion of the segment Xq13.3-q21.2

artículo científico publicado en 1992

Mapping the X chromosome breakpoint in two papillary renal cell carcinoma cell lines with a t(X;1)(p11.2;q21.2) and the first report of a female case.

artículo científico publicado en 1995

Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes

artículo científico publicado en 2012

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

artículo científico publicado en 2013

Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism

artículo científico publicado en 2008

Methylation and the fragile X

scientific article published in Nature

Mitochondrial and cytoplasmic forms of fumarate hydratase assigned to chromosome

artículo científico publicado en 1976

Mitochondrial and cytoplasmic forms of fumarate hydratase assigned to chromosome 1.

artículo científico publicado en 1976

Moderation of antidepressant response by the serotonin transporter gene.

artículo científico publicado en 2009

Moderation of breastfeeding effects on the IQ by genetic variation in fatty acid metabolism

artículo científico publicado en 2007

Moderation of the effect of adolescent-onset cannabis use on adult psychosis by a functional polymorphism in the catechol-O-methyltransferase gene: longitudinal evidence of a gene X environment interaction

artículo científico publicado en 2005

Molecular characterization of human X/Y translocations suggests their aetiology through aberrant exchange between homologous sequences on Xp and Yq

artículo científico publicado en 1989

Molecular cloning and tissue-specific expression of mouse kidney 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase

artículo científico publicado en 1996

Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint.

artículo científico publicado en 1996

Molecular genetics of blindness

artículo científico publicado en 1994

Molecular genetics of the X chromosome and X-linked diseases.

artículo científico publicado en 1986

Molecular heterogeneity of translocations associated with muscular dystrophy

artículo científico publicado en 1987

Molecular weight differences between human platelet and placental monoamine oxidase

artículo científico publicado en 1980

Multi-allelic RFLP for M27 beta, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255].

artículo científico publicado en 1987

Muscular dystrophy in girls with X;autosome translocations

artículo científico publicado en 1986

Mutations in the Norrie disease gene

artículo científico publicado en 1995

NRG1 gene in recurrent major depression: no association in a large-scale case-control association study

artículo científico publicado en 2010

Neural mechanisms of anger regulation as a function of genetic risk for violence

artículo científico publicado en 2009

New insights into the pharmacogenomics of antidepressant response from the GENDEP and STAR*D studies: rare variant analysis and high-density imputation.

artículo científico publicado en 2017

No association with the 5,10-methylenetetrahydrofolate reductase gene and major depressive disorder: results of the depression case control (DeCC) study and a meta-analysis

artículo científico publicado en 2008

Norrie disease gene: characterization of deletions and possible function

artículo científico publicado en 1993

Organization of the human genome

artículo científico publicado en 1994

Organization of the human monoamine oxidase genes and long-range physical mapping around them

artículo científico publicado en 1992

P2RX7: A bipolar and unipolar disorder candidate susceptibility gene?

artículo científico publicado en 2009

Pharmacogenetics of antidepressant response: A polygenic approach

artículo científico publicado en 2017

Pharmacoproteomic investigation into antidepressant response in two mouse inbred strains

artículo científico publicado en 2012

Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive Disorder

artículo científico publicado en 2015

Physical mapping of genes and sequences at the end of the human X chromosome short arm.

artículo científico publicado en 1987

Platelet monoamine oxidase: Specific activity and turnover number in schizophrenics and their families

article

Platelet monoamine oxidase: specific activity and turnover number in headache

article

Prediction of heterogeneity in intelligence and adult prognosis by genetic polymorphisms in the dopamine system among children with attention-deficit/hyperactivity disorder: evidence from 2 birth cohorts

artículo científico publicado en 2006

Presence of two forms of fumarase (fumarate hydratase E.C. 4.2.1.2) in mammalian cells: immunological characterization and genetic analysis in somatic cell hybrids. Confirmation of the assignment of a gene necessary for the enzyme expression to huma

artículo científico publicado en 1975

Probable assignment of the locus determining human red cell acid phosphatase ACP1 to chromosome 2 using somatic cell hybrids

artículo científico publicado en 1974

Proceedings: Analysis of the mitochondrial enzymes citrate synthase (EC 4.1.3.7) and malate dehydrogenase (EC 1.1.1.37) in human-mouse somatic cell hybrids

artículo científico publicado en 1974

Proceedings: Uptake of radioactive bacterial DNA by L929 mouse cells

artículo científico publicado en 1976

Proteins made in mitochondria of cultured animal cells

artículo científico publicado el 1 de enero de 1975

Psychiatric Genetics: Misbehaving monoamine oxidase gene

article

Psychiatry and the 'new genetics': hunting for genes for behaviour and drug response

artículo científico publicado en 2005

Quantitative trait loci for IQ and other complex traits: single-nucleotide polymorphism genotyping using pooled DNA and microarrays

artículo científico publicado en 2006

Quantitative trait locus analysis of candidate gene alleles associated with attention deficit hyperactivity disorder (ADHD) in five genes: DRD4, DAT1, DRD5, SNAP-25, and 5HT1B.

artículo científico publicado en 2005

Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children

artículo científico publicado en 2007

Report and abstracts of the Second International Workshop on Human Chromosome 12 mapping 1994. New Haven, Connecticut, June 20-22, 1994

scientific article published on 01 January 1994

Report of the committee on the genetic constitution of chromosome 12.

artículo científico publicado en 1990

Report of the committee on the genetic constitution of chromosomes 12 and 13.

artículo científico publicado en 1989

Report of the first international workshop on human chromosome 12 mapping

artículo científico publicado en 1992

Ribosomes from the blue-green alga Anabaena variabilis.

artículo científico publicado en 1967

Ribosomes from the blue-green alga Anabeana variabilis

artículo científico publicado en 1968

Role of genotype in the cycle of violence in maltreated children

artículo científico publicado en 2002

SNPs, microarrays and pooled DNA: identification of four loci associated with mild mental impairment in a sample of 6000 children

artículo científico publicado en 2005

Sequence analysis and transcript identification within 1.5 MB of DNA deleted together with the NDP and MAO genes in atypical Norrie disease patients presenting with a profound phenotype

artículo científico publicado en 2001

Sequence analysis of the breakpoint regions of an X;5 translocation in a female with Duchenne muscular dystrophy

artículo científico publicado en 1995

Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp

artículo científico publicado en 1997

Sex determination: zinc fingers point in the wrong direction

artículo científico publicado en 1990

Single-nucleotide polymorphism genotyping in DNA pools.

artículo científico publicado en 2005

Steroid sulphatase levels in XX males, including observations on two affected cousins

artículo científico publicado en 1981

Stressful life events and the brain-derived neurotrophic factor gene in bipolar disorder

artículo científico publicado en 2010

Stressful life events and the serotonin transporter gene (5-HTT) in recurrent clinical depression

artículo científico publicado en 2011

Structure of the human gene for monoamine oxidase type A.

artículo científico publicado en 1991

Studies of heterogeneous mitochondrial populations in a mouse cell line: the effects of selection for or against mitochondrial genomes that confer chloramphenicol resistance.

artículo científico publicado en 1985

Studies with deoxyribonucleic acid from blue-green algae

artículo científico publicado en 1969

THE CHARACTERIZATIO OF MONOAMINE OXIDASE IN CULTURED MAMMALIAN CELLS

artículo científico publicado en 1979

The Bipolar Association Case-Control Study (BACCS) and meta-analysis: No association with the 5,10-Methylenetetrahydrofolate reductase gene and bipolar disorder

artículo científico publicado en 2010

The MAO-A genotype does not modulate resting brain metabolism in adults

artículo científico publicado en 2008

The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3.

artículo científico publicado en 1992

The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

artículo científico publicado en 2006

The construction of human somatic cell hybrids containing portions of the mouse X chromosome and their use to generate DNA probes via interspersed repetitive sequence polymerase chain reaction

artículo científico publicado en 1991

The correlation between reading and mathematics ability at age twelve has a substantial genetic component

artículo científico publicado en 2014

The current state of play on the molecular genetics of depression

artículo científico

The dopamine D4 receptor and the hyperactivity phenotype: a developmental-epidemiological study.

artículo científico publicado en 2002

The genetic basis for sex differences in human behaviour: role of the sex chromosomes

artículo científico publicado en 2004

The genetics of affective disorder and suicide.

artículo científico publicado en 2010

The hypervariable DXS255 locus contains a LINE-1 repetitive element with a CpG island that is extensively methylated only on the active X chromosome

artículo científico publicado en 1992

The importance of stress and genetic variation in human aggression

artículo científico publicado en 2007

The interaction between child maltreatment, adult stressful life events and the 5-HTTLPR in major depression

artículo científico publicado en 2013

The isolation of an antimycin A-resistant human cell line.

artículo científico publicado en 1983

The mammalian Y chromosome: molecular search for the sex-determining gene--summary and perspectives

artículo científico publicado en 1987

The neuronal transporter gene SLC6A15 confers risk to major depression

artículo científico publicado en 2011

The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27ß methylation analysis

artículo científico publicado en 1990

The protective effect of the obesity-associated rs9939609 A variant in fat mass- and obesity-associated gene on depression

artículo científico publicado en 2012

The quantification of COMT mRNA in post mortem cerebellum tissue: diagnosis, genotype, methylation and expression

artículo científico publicado en 2006

The role of monoamine oxidase A, MAOA, in the aetiology of antisocial behaviour: the importance of gene-environment interactions.

artículo científico publicado en 2005

The serotonin transporter gene as a QTL for ADHD.

artículo científico publicado en 2005

Transcriptomics and the mechanisms of antidepressant efficacy

artículo científico publicado en 2015

Transient expression analysis of allelic variants of a VNTR in the dopamine transporter gene (DAT1)

artículo científico publicado en 2005

Tumor necrosis factor and its targets in the inflammatory cytokine pathway are identified as putative transcriptomic biomarkers for escitalopram response

artículo científico publicado en 2012

Two new mutations in exon 3 of theNDP gene: S73X and S101F associated with severe and less severe ocular phenotype, respectively

article

Utility of the pooling approach as applied to whole genome association scans with high-density Affymetrix microarrays

artículo científico publicado en 2010

Validation of single nucleotide polymorphism quantification in pooled DNA samples with SNaPIT. A glycosylase-mediated methods for polymorphism detection method

artículo científico publicado en 2002

Variation in GNB3 predicts response and adverse reactions to antidepressants

artículo científico publicado en 2010

Variation in regulation of steroid sulphatase locus in mammals

artículo científico publicado en 1983

Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27β

artículo científico publicado en 1992

X inactivation as a source of behavioural differences in monozygotic female twins

artículo científico publicado en 2004

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