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List of works by Hans Eiberg

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CHEK2 1100delC is prevalent in Swedish early onset familial breast cancer

scientific article published on 17 August 2007
GJB2 (Connexin-26) mutations are not frequent among hearing impaired patients in east Greenland

scientific article published on 27 February 2012
Genetic and phenotypic correlations between surrogate measures of insulin release obtained from OGTT data

scientific article
Major locus for red hair color linked to MNS blood groups on chromosome 4

article by Hans Eiberg & Jan Mohr published 28 June 2008 in Clinical Genetics
A novel mutation inIRF6 resulting in VWS–PPS spectrum disorder with renal aplasia

scientific article published on 01 June 2008
High brain serotonin levels in migraine between attacks: A 5-HT4 receptor binding PET study

scientific article published on 28 January 2018
A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.

scientific article published on 9 January 2008
Mutation analysis of the Sonic hedgehog promoter and putative enhancer elements in Parkinson's disease patients

scientific article published on 01 July 2004
Screening for Y microdeletions in men with testicular cancer and undescended testis.

scientific article published on January 2006
Mapping of hereditary trichilemmal cyst (TRICY1) to chromosome 3p24-p21.2 and exclusion of beta-CATENIN and MLH1

scientific article published on 01 February 2005
Associations of the Inflammatory Marker YKL-40 with Measures of Obesity and Dyslipidaemia in Individuals at High Risk of Type 2 Diabetes

scientific article
500K SNP array analyses in blood and saliva showed no differences in a pair of monozygotic twins discordant for cleft lip

scientific article published on 22 February 2011
LOH at chromosome 9q34.3 and the Notch1 gene methylation are less involved in oral squamous cell carcinomas

scientific article published on March 2007
Hereditary phenotypes in nocturnal enuresis

scientific article published on 28 June 2008
Autozygosity mapping of a large consanguineous Pakistani family reveals a novel non-syndromic autosomal recessive mental retardation locus on 11p15-tel

scientific article
Male-to-male transmission in Laurin-Sandrow syndrome and exclusion ofRARBandRARG

article
Frequency of the HFE C282Y and H63D mutations in Danish patients with clinical haemochromatosis initially diagnosed by phenotypic methods

scientific article published on December 2003
Determination of cis/trans phase of variations in the MC1R gene with allele-specific PCR and single base extension.

scientific article
Migraine is associated with high brain 5-HT levels as indexed by 5-HT4 receptor binding

scientific article published on 08 August 2018
Genetic evidence that HNF-1α–dependent transcriptional control of HNF-4α is essential for human pancreatic β cell function

article
Suggestive linkage to a neighboring region of IRF6 in a cleft lip and palate multiplex family

scientific article
Abdominal Wall Defects in Greenland 1989-2015

scientific article published on 2 May 2017
The ADULT-EEC spectrum: an R280C mutation with a borderline phenotype

scientific article published on 01 April 2007
Genetic Variations, Exposure to Persistent Organic Pollutants and Breast Cancer Risk - A Greenlandic Case-Control Study

scientific article published on 23 April 2018
ATXN2 with intermediate-length CAG/CAA repeats does not seem to be a risk factor in hereditary spastic paraplegia

scientific article published in October 2012
Genetic Correlation between Body Fat Percentage and Cardiorespiratory Fitness Suggests Common Genetic Etiology

scientific article
Family and population-based studies of variation within the ghrelin receptor locus in relation to measures of obesity

scientific article
The CHEK2 1100delC variant in Swedish colorectal cancer

scientific article published on 01 November 2006
The influence of parental history of diabetes and offspring birthweight on offspring glucose metabolism in adulthood

Full-field ERG in patients with Batten/Spielmeyer-Vogt disease caused by mutations in the CLN3 gene

article
The analysis of a large Danish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 11q24

scientific article published on September 1, 2015
RRP7A links primary microcephaly to dysfunction of ribosome biogenesis, resorption of primary cilia, and neurogenesis

scientific article published on 16 November 2020
Paroxysmal Cranial Dyskinesia and Nail-Patella Syndrome Caused by a Novel Variant in the LMX1B Gene

scientific article published on 19 September 2020
Heredity of supraglottic exercise-induced laryngeal obstruction

scientific article published on 17 August 2017
A splice-site variant in the lncRNA gene cosegregates in the large Volkmann cataract family

article
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Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter

scientific article published on 01 April 2003
Human leukocyte antigen association with familial steroid-sensitive nephrotic syndrome

scientific article published on 20 March 2020
From research to prevention in Greenland. Greenland Medical Society

scientific article published on 01 March 2007
Genetic insights into fetal growth and measures of glycaemic regulation and adiposity in adulthood: a family-based study

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