Hans Eiberg | Academic Influence

Hans Eiberg's AcademicInfluence.com Rankings

Hans Eiberg

Biology

#1376

World Rank

#2316

Historical Rank

Genetics

#154

World Rank

#193

Historical Rank

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Biology

Hans Eiberg's Degrees

PhD Genetics University of Copenhagen
Masters Biology University of Copenhagen

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Why Is Hans Eiberg Influential?

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According to Wikipedia, Hans Eiberg, is a Danish geneticist, known for his discovery of the genetic mutation causing blue eyes. Hans Eiberg graduated as a M.Sc. in 1970. He has worked with genetics at the Institute for Medical Biochemistry and Genetics of Copenhagen University since 1971, and became an associate professor at the institute in 1975.

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Hans Eiberg's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Cystic fibrosis locus defined by a genetically linked polymorphic DNA marker. (1985) (482)
Localization of cystic fibrosis locus to human chromosome 7cen–q22 (1985) (464)
Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression (2008) (314)
Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract (2002) (263)
Linkage studies of cholestasis familiaris groenlandica/Byler-like disease with polymorphic protein and blood group markers. (1993) (236)
A degradation-sensitive anionic trypsinogen (PRSS2) variant protects against chronic pancreatitis (2006) (229)
Cloning of a Human UDP-N-Acetyl-α-d-Galactosamine:PolypeptideN-Acetylgalactosaminyltransferase That Complements Other GalNAc-Transferases in Complete O-Glycosylation of the MUC1 Tandem Repeat* (1998) (210)
Blood-based biomarkers of age-associated epigenetic changes in human islets associate with insulin secretion and diabetes (2016) (187)
Dominant optic atrophy mapped to chromosome 3q region. II. Clinical and epidemiological aspects. (2009) (170)
Assignment of dominant inherited nocturnal enuresis (ENUR1) to chromosome 13q (1995) (163)
The genetics of enuresis: a review. (2001) (153)
Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I. Linkage analysis. (1994) (153)
Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios (2015) (148)
Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation (2016) (140)
Loss of the retinoblastoma protein-related p130 protein in small cell lung carcinoma. (1997) (138)
Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8. (2007) (129)
Autosomal dominant retinitis pigmentosa: linkage to rhodopsin and evidence for genetic heterogeneity. (1990) (125)
Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter (2002) (123)
Linkage relationships of paraoxonase (PON) with other markers: indication of PON‐cystic fibrosis synteny (1985) (123)
Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome) (2005) (119)
Sequencing and de novo assembly of 150 genomes from Denmark as a population reference (2017) (118)
Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene (2005) (113)
A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophy. (2002) (105)
Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6 (1987) (103)
New selective Giemsa technique for human chromosomes, Cd staining (1974) (101)
A missense mutation in FIC1 is associated with greenland familial cholestasis (2000) (98)
Batten disease (Spielmeyer-Vogt disease, juvenile onset neuronal ceroid-lipofuscinosis) gene (CLN3) maps to human chromosome 16. (1990) (97)
Comprehensive mutational screening in a cohort of Danish families with hereditary congenital cataract. (2009) (97)
Novel MODY3 Mutations in the Hepatocyte Nuclear Factor-1α Gene: Evidence for a Hyperexcitability of Pancreatic β-cells to Intravenous Secretagogues in a Glucose-Tolerant Carrier of a P447L Mutation (1997) (95)
Variants Near MC4R Are Associated With Obesity and Influence Obesity-Related Quantitative Traits in a Population of Middle-Aged People: Studies of 14,940 Danes (2009) (95)
Genetic evidence that HNF-1α–dependent transcriptional control of HNF-4α is essential for human pancreatic β cell function (2002) (94)
Deficiency of mannan-binding lectin associated serine protease-2 due to missense polymorphisms (2007) (93)
Genetic and epigenetic alterations of the blood group ABO gene in oral squamous cell carcinoma (2004) (92)
Novel Connexin 43 (GJA1) mutation causes oculo–dento–digital dysplasia with curly hair (2004) (89)
Human eye colour and HERC2, OCA2 and MATP. (2010) (86)
A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants (2017) (85)
Mutation analysis of the WFS1 gene in seven Danish Wolfram syndrome families; four new mutations identified (2005) (84)
Batten disease (Spielmeyer‐Sjogren disease) and haptoglobins (HP): indication of linkage and assignment to chr. 16 (1989) (81)
Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation (2004) (75)
Molecular genetics of nocturnal enuresis: clinical and genetic heterogeneity (1998) (75)
Assignment of Genes Coding for Brown Eye Colour (BEY2) and Brown Hair Colour (HCL3) on Chromosome 15q (1996) (73)
Partial and whole gene deletion mutations of the GCK and HNF1A genes in maturity-onset diabetes of the young (2007) (72)
Gentics and linkage relationships of the C3 polymorphism: discovery of C3‐Se linkage and assignment of LES‐C3‐DM‐Se‐PEPD‐Lu synteny to chromosome 19 (1983) (70)
Dyslexia and chromosome 15 heteromorphism: negative lod score in a Danish material (1987) (70)
A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect (2001) (68)
Polymorphisms in Phase I and Phase II genes and breast cancer risk and relations to persistent organic pollutant exposure: a case–control study in Inuit women (2014) (67)
Identification of novel and known mutations in the genes for keratin 5 and 14 in Danish patients with epidermolysis bullosa simplex: correlation between genotype and phenotype. (1999) (63)
Clinical enuresis phenotypes in familial nocturnal enuresis. (1997) (63)
A possible locus for manic depressive illness on chromosome 16p13 (1995) (63)
Total Genome Scan Analysis in a Single Extended Family for Primary Nocturnal Enuresis: Evidence for a NewLocus (ENUR3) for Primary Nocturnal Enuresis on Chromosome 22q11 (1998) (63)
CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24. (1997) (62)
Marner's cataract (CAM) assigned to chromosome 16: linkage to haptoglobin (1988) (61)
A survey of the newborn populations in Belgium, Germany, Poland, Czech Republic, Hungary, Bulgaria, Spain, Turkey, and Japan for the G985 variant allele with haplotype analysis at the medium chain Acyl-CoA dehydrogenase gene locus: clinical and evolutionary consideration. (1997) (60)
Novel mutation in ATP13A2 widens the spectrum of Kufor‐Rakeb syndrome (PARK9) (2012) (59)
Genetic evidence that HNF-1alpha-dependent transcriptional control of HNF-4alpha is essential for human pancreatic beta cell function. (2002) (58)
The functional Pro129Thr variant of the FAAH gene is not associated with various fat accumulation phenotypes in a population-based cohort of 5,801 whites (2007) (58)
Heterogeneity of FeNO response to inhaled steroid in asthmatic children (2003) (57)
Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study (1998) (57)
Autosomal dominant congenital cataract Morphology and genetic mapping (1989) (56)
Branchio–oto–renal syndrome: detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, MLPA and sequencing analyses (2007) (55)
Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36 (1995) (55)
A Survey of the Newborn Populations in Belgium, Germany, Poland, Czech Republic, Hungary, Bulgaria, Spain, Turkey, and Japan for the G985 Variant Allele with Haplotype Analysis at the Medium Chain Acyl-CoA (1997) (54)
Missense mutations in the human insulin promoter factor-1 gene and their relation to maturity-onset diabetes of the young and late-onset type 2 diabetes mellitus in caucasians. (2000) (52)
Genetic heterogeneity in Pakistani microcephaly families (2013) (52)
Cardiac involvement in myotonic dystrophy: a nationwide cohort study. (2014) (51)
Novel de novo BRCA2 mutation in a patient with a family history of breast cancer (2008) (51)
Assignment of Granular Corneal Dystrophy Groenouw Type I (CDGG1) to Chromosome 5q (1994) (50)
Preaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis-regulatory element ZRS (2010) (50)
The congenital "ant-egg" cataract phenotype is caused by a missense mutation in connexin46. (2006) (48)
Autosomal dominant congenital cataract; linkage relations; clinical and genetic heterogeneity (1992) (47)
Heat‐Shock Protein 70 Genes and Human Longevity (2006) (47)
Linkage between serum cholinesterase 2 (CHE2) and γ‐crystallin gene cluster (CRYG): assignment to chromosome 2 (1989) (45)
A novel nonsense mutation in PAX9 is associated with marked variability in number of missing teeth. (2007) (45)
Genetics of paraoxonase (1981) (44)
Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter (2003) (43)
Non-disjunction of chromosome 13. (2007) (42)
Mutational analysis of the human FATE gene in 144 infertile men (2003) (42)
Cytoplasmic expression of E-cadherin and beta-Catenin correlated with LOH and hypermethylation of the APC gene in oral squamous cell carcinomas. (2005) (42)
Compound heterozygous ASPM mutations in Pakistani MCPH families (2009) (41)
Variation in the gene encoding Krüppel-like factor 7 influences body fat: studies of 14 818 Danes. (2009) (40)
Susceptibility loci for bipolar affective disorder on chromosome 18? A review and a study of Danish families (1997) (40)
Autosomal inheritance of diabetes in two families characterized by obesity and a novel H241Q mutation in NEUROD1 (2008) (40)
A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family (2008) (38)
Genomic organization and chromosomal localization of three members of the UDP-N-acetylgalactosamine: polypeptide N-acetylgalactosaminyltransferase family. (1998) (37)
Novel MAF mutation in a family with congenital cataract-microcornea syndrome. (2007) (37)
Refinement of the dominant optic atrophy locus (OPA1) to a 1.4-cM interval on chromosome 3q28-3q29, within a 3-Mb YAC contig (1996) (35)
Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potential (2006) (35)
Genetic linkage of autosomal dominant primary open angle glaucoma to chromosome 3q in a Greek pedigree (2001) (35)
Nocturnal enuresis is linked to a specific gene. (1995) (35)
Linkage study of a large Danish 4-generation family with urge incontinence and nocturnal enuresis. (2001) (35)
Δ‐Aminolevulinatedehydrase: synteny with ABO‐AK1‐ORM (and assignment to chromosome 9) (1983) (34)
A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2 (2005) (32)
An exclusion map of Marfan syndrome. (1990) (32)
Molecular genetics of nocturnal enuresis: linkage to a locus on chromosome 22. (1999) (32)
A high frequent BRCA1 founder mutation identified in the Greenlandic population (2009) (31)
The myosin chaperone UNC45B is involved in lens development and autosomal dominant juvenile cataract (2014) (31)
Dominant optic atrophy in Denmark – report of 15 novel mutations in OPA1, using a strategy with a detection rate of 90% (2012) (30)
A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family (2010) (30)
Loss of heterozygosity at 9q33 and hypermethylation of the DBCCR1 gene in oral squamous cell carcinoma (2004) (30)
Gene for autosomal dominant congenital stationary night blindness maps to the same region as the gene for the beta-subunit of the rod photoreceptor cGMP phosphodiesterase (PDEB) in chromosome 4p16.3. (1994) (29)
Full-field ERG in patients with Batten/Spielmeyer-Vogt disease caused by mutations in the CLN3 gene (2000) (28)
Fasting and oral glucose-stimulated levels of glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) are highly familial traits (2012) (28)
RUNX2 analysis of Danish cleidocranial dysplasia families (2011) (27)
The Ala/Val98 polymorphism of the hepatocyte nuclear factor-1alpha gene contributes to the interindividual variation in serum C-peptide response during an oral glucose tolerance test: evidence from studies of 231 glucose-tolerant first degree relatives of type 2 diabetic probands. (1998) (27)
NeuroD / BETA 2 Gene Variability and Diabetes No Associations to Late-Onset Type 2 Diabetes but an A 45 Allele May Represent a Susceptibility Marker for Type 1 Diabetes Among Danes (2000) (27)
Linkage of transcobalamin II (TC2) to the P blood group system and assignment to chromosome 22 (1986) (26)
Proposal for the Nomenclature of Human Plasminogen (PLG) Polymorphism (1986) (26)
Structural organization of the human short-chain acyl-CoA dehydrogenase gene (1997) (26)
Assignment of human plasma methylumbelliferyl-tetra-N-acetylchitotetraoside hydrolase or chitinase to chromosome 1q by a linkage study (1997) (25)
Variation in CAPN10 in relation to type 2 diabetes, obesity and quantitative metabolic traits: studies in 6018 whites. (2006) (24)
Mitotic and meiotic instability of the CAG trinucleotide repeat in spinocerebellar ataxia type 1 (1998) (24)
A 72‐year‐old Danish puzzle resolved—comparative analysis of phenotypes in families with different‐sized HOXD13 polyalanine expansions (2005) (24)
Linkage between the loci for cystic fibrosis and paraoxonase (1986) (23)
RRP7A links primary microcephaly to dysfunction of ribosome biogenesis, resorption of primary cilia, and neurogenesis (2020) (23)
Heterogeneity in glucose response curves during an oral glucose tolerance test and associated cardiometabolic risk (2017) (23)
Orosomucoid polymorphism: Determination by Separator Isoelectric Focusing and Demonstration of ORM*F subtypes (1986) (22)
A polymorphic variant in the human electron transfer flavoprotein alpha-chain (alpha-T171) displays decreased thermal stability and is overrepresented in very-long-chain acyl-CoA dehydrogenase-deficient patients with mild childhood presentation. (1999) (22)
High brain serotonin levels in migraine between attacks: A 5-HT4 receptor binding PET study (2018) (22)
Differential nongenetic impact of birth weight versus third-trimester growth velocity on glucose metabolism and magnetic resonance imaging abdominal obesity in young healthy twins. (2011) (22)
Family and Population-Based Studies of Variation within the Ghrelin Receptor Locus in Relation to Measures of Obesity (2010) (21)
Mosaicism of the CAG repeat sequence in the Huntington disease gene in a pair of monozygotic twins (2004) (21)
Abstracts of workshop presentations (Part 2 of 16) (1987) (20)
A novel mutation in the epsilon-sarcoglycan gene causing myoclonus-dystonia syndrome. (2003) (19)
Abstracts of workshop presentations (Part 6 of 16) (1987) (19)
Epigenetic remodelling and dysregulation of DLGAP4 is linked with early-onset cerebellar ataxia (2014) (19)
Identity of the polymorphisms for esterase D and S-formylglutathione hydrolase in red blood cells (1986) (19)
Sequence variants in SPAST, SPG3A and HSPD1 in hereditary spastic paraplegia (2009) (19)
SATELLITE STAINING OF HUMAN CHROMOSOMES (1974) (18)
Hepatocyte nuclear factor-6: associations between genetic variability and Type II diabetes and between genetic variability and estimates of insulin secretion (1999) (18)
The CHEK2 1100delC variant in Swedish colorectal cancer. (2006) (18)
The effect of two frequent amino acid variants of the hepatocyte nuclear factor-1alpha gene on estimates of the pancreatic beta-cell function in Caucasian glucose-tolerant first-degree relatives of type 2 diabetic patients. (1998) (17)
Benchmarking the HLA typing performance of Polysolver and Optitype in 50 Danish parental trios (2018) (17)
Mapping of hereditary trichilemmal cyst (TRICY1) to chromosome 3p24‐p21.2 and exclusion of β‐CATENIN and MLH1 (2005) (17)
Associations of the Inflammatory Marker YKL-40 with Measures of Obesity and Dyslipidaemia in Individuals at High Risk of Type 2 Diabetes (2015) (17)
Dombrock blood group (DO): assignment to chromosome 12p (1996) (17)
Intermediate expansions of a GAA repeat in the frataxin gene are not associated with type 2 diabetes or altered glucose-induced beta-cell function in Danish Caucasians. (1999) (16)
Screening for Y microdeletions in men with testicular cancer and undescended testis (2006) (16)
G, R and C banding patterns of human chromosomes produced by heat treatment in organic and inorganic salt solutions (1973) (16)
Hereditary phenotypes in nocturnal enuresis (2008) (16)
Molecular genetic, clinical and psychiatric associations in nocturnal enuresis. (1998) (16)
Huntington's disease-like and ataxia syndromes: identification of a family with a de novo SCA17/TBP mutation. (2010) (16)
Linkage study between manic-depressive illness and chromosome 21. (1996) (16)
Frequency of the HFE C282Y and H63D mutations in Danish patients with clinical haemochromatosis initially diagnosed by phenotypic methods (2003) (15)
Suggestion of linkage between manic‐depressive illness and the enzyme phosphoglycolate phosphatase (PGP) on chromosome 16p (1993) (15)
A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia (2008) (14)
Linkage of Cholestasis Familiaris Groenlandica/Byler-like disease to chromosome 18. (2000) (14)
Genetic Correlation between Body Fat Percentage and Cardiorespiratory Fitness Suggests Common Genetic Etiology (2016) (14)
Report of the committee for chromosomes 17, 18, and 19. (1987) (13)
High heritability and genetic correlation of intravenous glucose- and tolbutamide-induced insulin secretion among non-diabetic family members of type 2 diabetic patients (2014) (13)
An MHC (HLA-A, -B, C2, BF, HLA-DR, GLO1) haplotype study of 497 Danish normal families with 1970 children including 97 twin pairs. (1990) (13)
Abdominal Wall Defects in Greenland 1989-2015. (2017) (13)
Linkage of plasma alpha-L-fucosidase (FUCA2) and the plasminogen (PLG) system. (1984) (13)
Antenatal genetic diagnosis in a kindred with a 15p+ chromosome (1973) (13)
Allele‐specific measurement of low‐density lipoprotein receptor transcript levels (1996) (12)
GJB2 (Connexin-26) mutations are not frequent among hearing impaired patients in East Greenland (2012) (12)
Assignment of GUCY1B2, the gene coding for the beta2 subunit of human guanylyl cyclase to chromosomal band 13q14.3 between markers D13S168 and D13S155. (1999) (12)
Genetic studies in congenital anterior midline cervical cleft (2012) (12)
CHEK2 1100delC is prevalent in Swedish early onset familial breast cancer (2007) (12)
Migraine is associated with high brain 5-HT levels as indexed by 5-HT4 receptor binding (2018) (11)
Determination of cis/trans phase of variations in the MC1R gene with allele‐specific PCR and single base extension (2008) (11)
Risk of cancer in relatives of patients with myotonic dystrophy: a population‐based cohort study (2014) (11)
35th Annual meeting of the European Association for the Study of Diabetes. Brussels, Belgium, 28 September-2 October, 1999. Abstracts. (1999) (11)
A novel mutation in IRF6 resulting in VWS–PPS spectrum disorder with renal aplasia (2008) (10)
Colton blood groups: indication of linkage with the Kidd (Jk) system as support for assignment to chromosome 7 (1977) (10)
A silent A to G mutation in exon 11 of the medium-chain acyl-CoA dehydrogenase (MCAD) gene. (1993) (10)
Abstracts of workshop presentations (Part 12 of 16) (1987) (10)
Confirmation of F13A assignment and sequence information concerning F13A‐HLA‐GLO (1984) (9)
Linkage analysis between manic-depressive illness and markers on the long arm of chromosome 11. (1995) (9)
The g/a Nucleotide Variant at Position −30 in the β-Cell-Specific Glucokinase Gene Promoter Has No Impact on the β-Cell Function in Danish Caucasians (1998) (9)
ATXN2 with intermediate-length CAG/CAA repeats does not seem to be a risk factor in hereditary spastic paraplegia (2012) (9)
Abstracts of workshop presentations (Part 15 of 16) (1987) (8)
Cholestasis Familiaris Groenlandica: an epidemiological, clinical and genetic study. (2004) (8)
Polymorphic drug metabolizing CYP-enzymes--a pathogenic factor in oral lichen planus? (2008) (8)
Cholestasis Familiaris Groelandica: an epidemiological, clinical and genetic study (2004) (8)
Linkage analysis between manic-depressive illness and 35 classical markers. (1994) (8)
A search for genes predisposing to manic depressive illness on chromosome 20 (1995) (8)
Male‐to‐male transmission in Laurin–Sandrow syndrome and exclusion of RARB and RARG (2005) (8)
Cholestasis Familiaris Groenlandica/ Byler-like disease in Greenland — A population study (2004) (8)
Autozygosity mapping of a large consanguineous Pakistani family reveals a novel non-syndromic autosomal recessive mental retardation locus on 11p15-tel (2011) (7)
Abstracts of workshop presentations (Part 10 of 16) (1987) (7)
Suggestive linkage to a neighboring region of IRF6 in a cleft lip and palate multiplex family (2007) (7)
Genetic and phenotypic correlations between surrogate measures of insulin release obtained from OGTT data (2015) (7)
Linkage analysis between manic depressive illness and the dopamine beta‐hydroxylase gene (1994) (7)
No evidence of linkage between manic depressive illness and the dopa decarboxylase gene or nearby region on chromosome 7p (1995) (6)
500K SNP array analyses in blood and saliva showed no differences in a pair of monozygotic twins discordant for cleft lip (2011) (6)
Genetic heterogeneity in nocturnal enuresis. (1997) (5)
Genetic Variations, Exposure to Persistent Organic Pollutants and Breast Cancer Risk – A Greenlandic Case–Control Study (2018) (5)
Another case of a lymphocytotoxic antibody with blood group A1 Leb and A Led associated specificity. (2008) (5)
The ADULT‐EEC spectrum: An R280C mutation with a borderline phenotype (2007) (5)
Mutation analysis of the Sonic hedgehog promoter and putative enhancer elements in Parkinson's disease patients. (2004) (5)
LOH at chromosome 9q34.3 and the Notch1 gene methylation are less involved in oral squamous cell carcinomas. (2007) (5)
The analysis of a large Danish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 11q24 (2015) (5)
Abstracts of workshop presentations (Part 7 of 16) (1987) (4)
Some lod scores concerning chromosome 1. (1976) (4)
Abstracts of workshop presentations (Part 1 of 16) (1987) (4)
Determination of common haptoglobin phenotypes in Egyptians and Danes by means of non-carcinogenic stain reagents. (2008) (4)
Cystic fibrosis; hint of linkage with F13B (1985) (4)
Abstracts of workshop presentations (Part 3 of 16) (1987) (4)
Abstracts of workshop presentations (Part 4 of 16) (1987) (3)
Linkage between alpha 1B-glycoprotein (A1BG) and Lutheran (LU) red blood group system: assignment to chromosome 19: new genetic variants of A1BG. (1989) (3)
Evidence for a serotonergic subtype of major depressive disorder: A NeuroPharm-1 study. (2020) (3)
[Epidermolysis bullosa simplex: genotype-phenotype correlation in Danish patients]. (2000) (3)
Heredity of supraglottic exercise-induced laryngeal obstruction (2017) (3)
The influence of parental history of diabetes and offspring birthweight on offspring glucose metabolism in adulthood (2011) (3)
Human leukocyte antigen association with familial steroid-sensitive nephrotic syndrome (2020) (3)
The g/a nucleotide variant at position -30 in the beta-cell-specific glucokinase gene promoter has no impact on the beta-cell function in Danish Caucasians. (1998) (3)
Number of loci responsible for the inheritance of high and low activity of paraoxonase (1986) (3)
Genetic screening of 15 SNPs in the MC1R gene in relation to hair colour in Danes (2006) (3)
Abstracts of workshop presentations (Part 8 of 16) (1987) (3)
Paroxysmal Cranial Dyskinesia and Nail‐Patella Syndrome Caused by a Novel Variant in the LMX1B Gene (2020) (3)
Abstracts of workshop presentations (Part 11 of 16) (1987) (2)
Abstracts of workshop presentations (Part 5 of 16) (1987) (2)
Abstracts of workshop presentations (Part 14 of 16) (1987) (2)
Sex ratios, HLA markers, and rheumatic diseases. (1992) (2)
A splice-site variant in the lncRNA gene RP1-140A9.1 cosegregates in the large Volkmann cataract family (2019) (1)
Abstracts of workshop presentations (Part 9 of 16) (1987) (1)
Genetic insights into fetal growth and measures of glycaemic regulation and adiposity in adulthood: a family-based study (2018) (1)
Using mtDNA to evaluate pioneer colonization scenarios for early prehistoric southern Scandinavia (2013) (1)
[Preclinical and prenatal diagnosis of familial adenomatous polyposis]. (1992) (1)
Abstracts of workshop presentations (Part 16 of 16) (1987) (1)
Alexander F. Zakharov (1986) (1)
Antenatal genetic diagnosis in a kindred with a 15p plus chromosome. (1973) (1)
Branchio-Oto-Renal Syndrome: Detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, sequencing and MLPA analyses (2007) (1)
Serotonin 4 Receptor Brain Binding in Major Depressive Disorder and Association With Memory Dysfunction. (2023) (1)
Neonatal and Maternal Lymphocytes in Whole‐Blood Cultures: Absence of Strong Interaction (1978) (1)
Hepatocyte nuclear factor-6: Studies of associations between genetic variability and type 2 diabetes or estimates of insulin secretion (1999) (0)
Subject index Vol. 46, 1987 (1987) (0)
Some iod scores concerning chromosome 1. (1976) (0)
Identification of novel locus at chromosome 3p12.3‐q13.31 for autosomal recessive intellectual disability in a consanguineous family (2014) (0)
[From research to prevention in Greenland. Greenland Medical Society]. (2007) (0)
RRP7A links primary microcephaly to radial glial cells and dysfunction of ribosomal biogenesis, neurogenesis and ciliary resorption (2019) (0)
Molecular characterization of four new mutations in the genes for keratin 5 and 14 associated with the disease epidermolysis bullosa simplex in 7 seemingly unrelated patients (1998) (0)
Contents, Vol. 46, 1987/ Title Page / Table of Contents (1987) (0)
P-108: Phenotype characteristics of two Danish MODY families with linkage to chromosome 12 (2009) (0)
Mere om Genetik og høsommerfugle. Ikke Mendelsk arvegang af farven hos orange høsommerfugl Colias croceus Geoffr (2017) (0)
Polymorphisms in Phase I and Phase II genes and breast cancer risk and relations to persistent organic pollutant exposure in Inuit and Danish women (2015) (0)
[Identification of human chromosomes. A review of a new staining methods and their field of application]. (1973) (0)
Late Breaking Posters (2003) (0)
Author and Subject Index (1998) (0)
Subject Index Vol. 16, 1976 (1976) (0)
A genome-wide association study of IVGTT-based measures of first phase insulin secretion refines the underlying physiology of type 2 diabetes variants Mechanisms of type 2 diabetes genetic risk factors (2017) (0)
Subject Index Vol. 41, 1986 (2004) (0)
Mapping status of cystic fibrosis (1986) (0)
Genetic polymorphisms of enzymes involved in xenobiotic metabolism among Greenlandic Inuit (2011) (0)
The analysis of a large Danish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 11q24 (2015) (0)
Benchmarking the HLA typing performance of Polysolver and Optitype in 50 Danish parental trios (2018) (0)
Abstracts of workshop presentations (Part 13 of 16) (1987) (0)
Familial Steroid Sensitive Nephrotic Syndrome: Linkage data to Chromosome 15 and 6 (2016) (0)
Letter: Satellite staining of human chromosomes. (1974) (0)
Transferrin subtypes in 51 Danish patients with hereditary haemochromatosis and in 847 normal subjects (1992) (0)
A family with ulcerative colitis maps to 7p21.1 and comprises a region with regulatory activity for the aryl hydrocarbon receptor gene. (2023) (0)
Fasting and oral glucose-stimulated levels of GIP and GLP-1 are highly familial traits (2012) (0)
Reply (2016) (0)
Syv års screening for CFG og PCCB (2013) (0)
Full-field ERG in patients with Spielmeyer-Vogt/Batten disease caused by mutations in the CLN3 gene (1999) (0)

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