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List of works by Margit Burmeister

A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome

scientific article published on 01 June 2020

Alterations in cerebellar physiology are associated with a stiff-legged gait in Atcay(ji-hes) mice

scientific article

Antisense expression of the human pro-melanin-concentrating hormone genes

scientific article published in August 1998

Antisocial alcoholism and serotonin-related polymorphisms: association tests.

scientific article published on September 2002

Association between Val66Met brain-derived neurotrophic factor (BDNF) gene polymorphism and post-treatment relapse in alcohol dependence

scientific article

Association between a dopamine-4 receptor polymorphism and blood pressure.

scientific article published in September 2005

Association of the DYX1C1 dyslexia susceptibility gene with orthography in the Chinese population

scientific article

BDNF Val(66)Met genotype is associated with drug-seeking phenotypes in heroin-dependent individuals: a pilot study

scientific article

BDNF Val66Met allele is associated with reduced hippocampal volume in healthy subjects

scientific article published on 25 January 2006

Bayesian EM algorithm for scoring polymorphic deletions from SNP data and application to a common CNV on 8q24.

scientific article

COQ4 Mutation Leads to Childhood-Onset Ataxia Improved by CoQ10 Administration

scientific article published on 01 June 2019

Characterization of a mutagenic B1 retrotransposon insertion in the jittery mouse

scientific article published in July 2004

Chromosomal localization of the ankyrinG gene (ANK3/Ank3) to human 10q21 and mouse 10

scientific article

Commentary on “Occupational Noise, Smoking and a High Body Mass Index are Risk Factors for Age-Related Hearing Impairment and Moderate Alcohol Consumption is Protective: a European Population-Based Multicentre Study” by Fransen et al., J. Assoc. Res

scientific article

Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpoints

scientific article

Complete cDNAs for CDC42 from chicken cochlea and mouse liver

scientific article published in June 1997

Construction of Lambda Libraries from Large PFGE Fragments

scientific article published on January 1, 1992

Corrigendum: Serotonin transporter gene, stress, and raphe–raphe interactions: a molecular mechanism of depression

scientific article published in July 2012

DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24.

scientific article

Development of additional RFLP probes near the locus for Duchenne muscular dystrophy by cosmid cloning of the DXS84 (754) locus

article

Diaphanous homolog 3 (Diap3) overexpression causes progressive hearing loss and inner hair cell defects in a transgenic mouse model of human deafness

scientific article

Dominant Mutation of CCDC78 in a Unique Congenital Myopathy with Prominent Internal Nuclei and Atypical Cores ⬇️

scientific article published on July 19, 2012

Effects of the serotonin transporter gene, sensitivity of response to alcohol, and parental monitoring on risk for problem alcohol use.

scientific article

Encyclopedia of the mouse genome VII. Mouse chromosome 10.

scientific article published in January 1998

Evaluation of exome sequencing variation in undiagnosed ataxias

scientific article published on 4 April 2015

Expression of Caytaxin protein in Cayman Ataxia mouse models correlates with phenotype severity

scientific article (publication date: 2012)

Familiality and diagnostic patterns of subphenotypes in the National Institutes of Mental Health bipolar sample

scientific article published in January 2008

Family-based SNP association study on 8q24 in bipolar disorder

scientific article published on July 2008

Family-based association analysis to finemap bipolar linkage peak on chromosome 8q24 using 2,500 genotyped SNPs and 15,000 imputed SNPs.

scientific article published on December 2010

Fine genetic and comparative mapping of the deafness mutation Ames waltzer on mouse chromosome 10

scientific journal article

Fine genetic map of mouse chromosome 10 around the polycystic kidney disease gene, jcpk, and ankyrin 3.

scientific article published in August 1996

Fluorescence in situ hybridization establishes the order cen-DXS28(C7)-DXS67(B24)-DXS68(L1)-tel in human chromosome Xp21.3.

scientific article

Functional mu opioid receptor polymorphism (OPRM1 A(118) G) associated with heroin use outcomes in Caucasian males: A pilot study

scientific article published on 24 April 2015

Future of genetics of mood disorders research

scientific article

G to C transversion at a splice acceptor site causes exon skipping in the cystatin B gene

scientific article published on September 1997

Genes and genetic testing in hereditary ataxias.

scientific article

Genetic analysis of the neuronal and ubiquitous AP-3 adaptor complexes reveals divergent functions in brain.

scientific article

Genetic and phenotypic analysis of the mouse mutant mh2J, an Ap3d allele caused by IAP element insertion.

scientific article published in March 2003

Genetic map of the region around grizzled (gr) and mocha (mh) on mouse chromosome 10, homologous to human 19p13.3.

scientific article published in October 1994

Genetic research on complex behaviors: An examination of attempts to identify genes for smoking

article

Genetical genomics: combining genetics with gene expression analysis

scientific article

Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry

scientific journal article

Genome-wide association scan for five major dimensions of personality

scientific article

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genomic prediction of depression risk and resilience under stress

scientific article published on 28 October 2019

High-yield DNA preparation from liquid phage lambda cultures

scientific article published in October 1996

Hippocampal auditory gating in the hyperactive mocha mouse

scientific article published in November 1999

Identification of a novel LIM domain gene, LMCD1, and chromosomal localization in human and mouse

scientific article published on January 2000

Identification of polymorphisms by genomic denaturing gradient gel electrophoresis: application to the proximal region of human chromosome 21 ⬇️

scientific article published on April 11, 1991

Impulsiveness and insula activation during reward anticipation are associated with genetic variants in GABRA2 in a family sample enriched for alcoholism ⬇️

scientific article published on April 12, 2011

Increased activity of Diaphanous homolog 3 (DIAPH3)/diaphanous causes hearing defects in humans with auditory neuropathy and in Drosophila

scientific article

Indirect effect of corticotropin-releasing hormone receptor 1 gene variation on negative emotionality and alcohol use via right ventrolateral prefrontal cortex.

scientific article published on March 2014

Influence of Threat and Serotonin Transporter Genotype on Interference Effects ⬇️

scientific article published on May 10, 2012

Interpretation of linkage data for a Huntington-like disorder mapping to 4p15.3.

scientific article published on July 2000

Isolation and Characterization of Several Members of the Murine Hsd3b Gene Family

article

Jekyll, a family of phage-plasmid shuttle vectors

scientific article published on 01 December 1988

Long-range restriction map around the Duchenne muscular dystrophy gene

scientific article published in Nature

Mapping of genetic modifiers affecting the eye phenotype of ocular retardation (Chx10or-J) mice

scientific article published on 12 June 2006

Mapping of the neural retina leucine zipper gene, Nrl, to mouse chromosome 14.

scientific article published in January 1993

Meta-analysis of the association between a serotonin transporter promoter polymorphism (5-HTTLPR) and anxiety-related personality traits

scientific article

MicroRNA expression changes in lymphoblastoid cell lines in response to lithium treatment

scientific article published on 2 March 2009

Mitochondrial related gene expression changes are sensitive to agonal-pH state

article

Mitochondrial-related gene expression changes are sensitive to agonal-pH state: implications for brain disorders

scientific article

Mouse chromosome 10

scientific article published in January 1997

Mouse chromosome 10

scientific article published on 01 January 1993

Mouse chromosome 10.

scientific article published in October 1999

Mouse models for psychiatric disorders.

scientific article

Mutation in AP-3 delta in the mocha mouse links endosomal transport to storage deficiency in platelets, melanosomes, and synaptic vesicles

scientific article

Mutation in ATG5 reduces autophagy and leads to ataxia with developmental delay.

scientific article published on 26 January 2016

Mutations in KCND3 cause spinocerebellar ataxia type 22.

scientific article

Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects

scientific article published on 31 March 2018

Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse.

scientific article published on 12 October 2003

Neuronal and non-neuronal functions of the AP-3 sorting machinery

scientific article published on February 2007

Neuropeptide Y and representation of salience in human nucleus accumbens

scientific article published on 02 October 2018

New insights into the genetics of addiction

scientific article

No association between DFNA6 and Pro250Arg mutation in FGFR3.

scientific article published in October 1999

Novel cystatin B mutation and diagnostic PCR assay in an unverricht-lundborg progressive myoclonus epilepsy patient ⬇️

scientific article published on September 19, 1997

Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation

scientific journal article

PER3 polymorphism and insomnia severity in alcohol dependence

scientific article published on April 2012

PFGE Using Double-Inhomogeneous Fields or Orthogonal Field-Alternating Gel Electrophoresis (OFAGE)

scientific article published on 01 January 1992

Partial rescue of the ocular retardation phenotype by genetic modifiers

scientific article published on 01 February 2000

Pathogenesis of clinical signs in recessive ataxia with saccadic intrusions

scientific article published in December 2003

Photoreceptor degeneration and rd1 mutation in the grizzled/mocha mouse strain

scientific article published in April 2003

Physical mapping of yeast artificial chromosomes containing sequences from the human beta-globin gene region

scientific article published on August 1991

Possible association between response inhibition and a variant in the brain-expressed tryptophan hydroxylase-2 gene

scientific article published in February 2006

Protocol for a collaborative meta-analysis of 5-HTTLPR, stress, and depression

scientific article

Psychiatric genetics: progress amid controversy

scientific article

SNPs on Chips: The Hidden Genetic Code in Expression Arrays

scientific article published on 11 May 2006

SSRI response in depression may be influenced by SNPs in HTR1B and HTR1A.

scientific article published on December 2009

Serotonin transporter gene, stress and raphe-raphe interactions: a molecular mechanism of depression

scientific article published on 31 January 2012

Severe vestibular and auditory impairment in three alleles of Ames waltzer (av) mice

scientific journal article

Strategies for Mapping Large Regions of Mammalian Genomes

scientific article published on 01 January 1992

Susceptibility effects of GABA receptor subunit alpha-2 (GABRA2) variants and parental monitoring on externalizing behavior trajectories: Risk and protection conveyed by the minor allele.

scientific article

Taql RFLP at D21S137 ⬇️

scientific article published on July 25, 1991

The CC genotype in HTR2A T102C polymorphism is associated with behavioral impulsivity in alcohol-dependent patients

scientific article published on 17 September 2011

The CC genotype in the T102C HTR2A polymorphism predicts relapse in individuals after alcohol treatment

scientific article published on 12 January 2013

The Collaborative Cross, a community resource for the genetic analysis of complex traits

article

The Effect of Question Framing and Response Options on the Relationship between Racial Attitudes and Beliefs about Genes as Causes of Behavior.

scientific article

The Neurological Mouse Mutations Jittery and Hesitant Are Allelic and Map to the Region of Mouse Chromosome 10 Homologous to 19p13.3

scientific article published on 01 August 1996

The mouse glutathione peroxidase Gpx2 gene maps to chromosome 12; its pseudogene Gpx2-ps maps to chromosome 7.

scientific article published on May 1996

The serotonin transporter promoter variant (5-HTTLPR), stress, and depression meta-analysis revisited: evidence of genetic moderation

scientific article

Tissue-specific functional networks for prioritizing phenotype and disease genes

scientific article

Visualization of DNA in agarose gels as migrating colored bands: applications for preparative gels and educational demonstrations

scientific article published in August 1996

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