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1

Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within theHERC2gene inhibitingOCA2expression

Hans Eiberg, Jesper Troelsen, Mette Nielsen, Annemette Mikkelsen, Jonas Mengel-From, Klaus W. Kjaer, Lars Hansen

Journal:

Year:

2008

Language:

english

File:

PDF, 829 KB

english, 2008

2

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

Hans Eiberg, Jan Mohr

Journal:

Clinical Genetics

Year:

1987

Language:

english

File:

PDF, 248 KB

english, 1987

3

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

Ghisari, Mandana, Eiberg, Hans, Long, Manhai, Bonefeld-Jørgensen, Eva C

Journal:

Environmental Health

Year:

2014

Language:

english

File:

PDF, 468 KB

english, 2014

4

Linkage study between manic-depressive illness and chromosome 21

Ewald, Henrik, Eiberg, Hans, Mors, Ole, Flint, Tracey, Kruse, Torben A.

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 617 KB

english, 1996

5

Linkage analysis between manic-depressive illness and 35 classical markers

Dr. Henrik Ewald, Ole Mors, Hans Eiberg

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 542 KB

english, 1994

6

Determination of cis/trans phase of variations in the MC1R gene with allele-specific PCR and single base extension

Jonas Mengel-From, Claus Børsting, Juan J. Sanchez, Hans Eiberg, Niels Morling

Journal:

ELECTROPHORESIS

Year:

2008

Language:

english

File:

PDF, 215 KB

english, 2008

7

Human eye colour and HERC2, OCA2 and MATP

Jonas Mengel-From, Claus Børsting, Juan J. Sanchez, Hans Eiberg, Niels Morling

Journal:

Forensic Science International: Genetics

Year:

2010

Language:

english

File:

PDF, 151 KB

english, 2010

8

Autosomal dominant retinitis pigmentosa: Linkage to rhodopsin and evidence for genetic heterogeneity

Jane Farrar, G., McWilliam, Peter, Bradley, Daniel G., Kenna, Paul, Lawler, Mark, Sharp, Elizabeth M., Humphries, Marian M., Eiberg, Hans, Micheal Conneally, P., Trofatter, James A.

Journal:

Year:

1990

Language:

english

File:

PDF, 716 KB

english, 1990

9

THE GENETICS OF ENURESIS: A REVIEW

von GONTARD, ALEXANDER, SCHAUMBURG, HENRITTE, HOLLMANN, ELKE, EIBERG, HANS, RITTIG, SØREN

Journal:

The Journal of Urology

Year:

2001

Language:

english

File:

PDF, 74 KB

english, 2001

10

Genetic Variations, Exposure to Persistent Organic Pollutants and Breast Cancer Risk: A Greenlandic Case-Control Study

Wielsøe, Maria, Eiberg, Hans, Ghisari, Mandana, Kern, Peder, Lind, Ole, Bonefeld-Jørgensen, Eva Cecilie

Journal:

Basic & Clinical Pharmacology & Toxicology

Year:

2018

Language:

english

File:

PDF, 315 KB

english, 2018

11

Human leukocyte antigen association with familial steroid-sensitive nephrotic syndrome

Korsgaard, Trine, Joshi, Shivani, Andersen, Rene F., Moeller, Kristina, Seeman, TomÃ¡s, PodrackÃ¡, Ludmila, Eiberg, Hans, Rittig, SÃ¸ren

Journal:

European Journal of Pediatrics

Year:

2020

Language:

english

File:

PDF, 1.05 MB

english, 2020

12

Allele-specific measurement of low-density lipoprotein receptor transcript levels

Lillian G. Jensen, Henrik K. Jensen, Finn Heath, Hans Eiberg, Margrethe Kjeldsen, Ole Færgeman, Steen Kølvraa, Lars Bolund, Niels Gregersen

Journal:

Year:

1996

Language:

english

File:

PDF, 667 KB

english, 1996

13

Linkage analysis between manic-depressive illness and markers on the long arm of chromosome 11

Henrik Ewald, Ole Mors, Tracey Flint, Ursula Friedrich, Hans Eiberg, Torben A. Kruse

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 691 KB

english, 1995

14

Novel Connexin 43 (GJA1) mutation causes oculo–dento–digital dysplasia with curly hair

Klaus W. Kjaer, Lars Hansen, Hans Eiberg, Pernille Leicht, John M. Opitz, Niels Tommerup

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 149 KB

english, 2004

15

Mosaicism of the CAG repeat sequence in the Huntington disease gene in a pair of monozygotic twins

Anne Nørremølle, Lis Hasholt, Cathrine Bie Petersen, Hans Eiberg, Steen G. Hasselbalch, Peter Gideon, Jørgen E. Nielsen, Sven Asger Sørensen

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 164 KB

english, 2004

16

Mapping of hereditary trichilemmal cyst (TRICY1) to chromosome 3p24-p21.2 and exclusion of β-CATENIN and MLH1

Hans Eiberg, Lars Hansen, Claus Hansen, Jan Mohr, Peter Stubbe Teglbjærg, Klaus Wilbrandt Kjaer

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 194 KB

english, 2005

17

Male-to-male transmission in Laurin–Sandrow syndrome and exclusion of RARB and RARG

Klaus W. Kjaer, Lars Hansen, Hans Eiberg, Knud Stenild Christensen, John M. Opitz, Niels Tommerup

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 160 KB

english, 2005

18

A 72-year-old Danish puzzle resolved—comparative analysis of phenotypes in families with different-sized HOXD13 polyalanine expansions

Klaus W. Kjaer, Lars Hansen, Hans Eiberg, Algirdas Utkus, Lene T. Skovgaard, Pernille Leicht, John M. Opitz, Niels Tommerup

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 211 KB

english, 2005

19

The ADULT-EEC spectrum: An R280C mutation with a borderline phenotype

Elisa Kier-Swiatecka, Marianne Kock, Peter Marker, Hans Eiberg, Klaus Wilbrandt Kjaer

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 182 KB

english, 2007

20

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

Linda P. Jakobsen, Reinhard Ullmann, Klaus W. Kjaer, Mary A. Knudsen, Niels Tommerup, Hans Eiberg

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 175 KB

english, 2007

21

A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family

Kirsten M. Sanggaard, Klaus W. Kjaer, Hans Eiberg, Gudrun Nürnberg, Peter Nürnberg, Katrin Hoffman, Hanne Jensen, Charlotte Sørum, Nanna D. Rendtorff, Lisbeth Tranebjærg

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 472 KB

english, 2008

22

A novel mutation in IRF6 resulting in VWS–PPS spectrum disorder with renal aplasia

Filipe de Medeiros, Lars Hansen, Evete Mawlad, Hans Eiberg, Camilla Asklund, Niels Tommerup, Linda P. Jakobsen

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 156 KB

english, 2008

23

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

Linda P. Jakobsen, Merete Bugge, Reinhard Ullmann, Charlotte K. Schjerling, Rehannah Borup, Lars Hansen, Hans Eiberg, Niels Tommerup

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 85 KB

english, 2011

24

Analysis of connexin expression during mouse Schwann cell development identifies Connexin29 as a novel marker for the transition of neural crest to precursor cells

Jing Li, Hans-Werner Habbes, Jürgen Eiberger, Klaus Willecke, Rolf Dermietzel, Carola Meier

Journal:

Year:

2007

Language:

english

File:

PDF, 895 KB

english, 2007

25

Genetic and epigenetic alterations of the blood group ABO gene in oral squamous cell carcinoma

Shan Gao, Jesper Worm, Per Guldberg, Hans Eiberg, Annelise Krogdahl, Chung-Ji Liu, Jesper Reibel, Erik Dabelsteen

Journal:

International Journal of Cancer

Year:

2004

Language:

english

File:

PDF, 363 KB

english, 2004

26

Novelde novo BRCA2mutation in a patient with a family history of breast cancer

Thomas V O Hansen, Marie Luise Bisgaard, Lars Jønson, Anders Albrechtsen, Bettina Filtenborg-Barnkob, Hans Eiberg, Bent Ejlertsen, Finn C Nielsen

Journal:

BMC Medical Genetics

Year:

2008

Language:

english

File:

PDF, 1.02 MB

english, 2008

27

Studies on a new group of biodegradable surfactants for glyphosate

Roland Haefs, Michaela Schmitz-Eiberger, Hans-G Mainx, Werner Mittelstaedt, Georg Noga

Journal:

Pest Management Science

Year:

2002

Language:

english

File:

PDF, 189 KB

english, 2002

28

Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36

Hans Eiberg, Allan Meldgaard Lund, Mette Warburg, Thomas Rosenberg

Journal:

Year:

1995

Language:

english

File:

PDF, 469 KB

english, 1995

29

Transferrin subtypes in 51 Danish patients with hereditary haemochromatosis and in 847 normal subjects

Nils Milman, Hans Eiberg, Mariann Thymann, Kirsten Fenger

Journal:

Year:

1992

Language:

english

File:

PDF, 175 KB

english, 1992

30

The functional Pro129Thr variant of theFAAHgene is not associated with various fat accumulation phenotypes in a population-based cohort of 5,801 whites

Dorit P. Jensen, Camilla H. Andreasen, Mette K. Andersen, Lars Hansen, Hans Eiberg, Knut Borch-Johnsen, Torben Jørgensen, Torben Hansen, Oluf Pedersen

Journal:

Journal of Molecular Medicine

Year:

2007

Language:

english

File:

PDF, 138 KB

english, 2007

31

Structural organization of the human short-chain acyl-CoA dehydrogenase gene

Morten Juhl Corydon, Brage Storstein Andresen, Peter Bross, Margrethe Kjeldsen, Per Hove Andreasen, Hans Eiberg, Steen Kølvraa, Nils Gregersen

Journal:

Mammalian Genome

Year:

1997

Language:

english

File:

PDF, 1.54 MB

english, 1997

32

Genomic structure of the human mitochondrial chaperonin genes: HSP60 andHSP10are localised head to head on chromosome

Jens J. Hansen, Peter Bross, Majken Westergaard, Marit Nielsen, Hans Eiberg, Anders D. Børglum, Jens Mogensen, Karsten Kristiansen, Lars Bolund, Niels Gregersen

Journal:

Year:

2003

Language:

english

File:

PDF, 101 KB

english, 2003

33

Mutational analysis of the human FATE gene in 144 infertile men

Christian Olesen, Joachim Silber, Hans Eiberg, Erik Ernst, Karsten Petersen, Svend Lindenberg, Niels Tommerup

Journal:

Year:

2003

Language:

english

File:

PDF, 247 KB

english, 2003

34

Refinement of the dominant optic atrophy locus (OPA1) to a 1.4-cM interval on chromosome 3q28-3q29, within a 3-Mb YAC contig

A. Jonasdottir, Hans Eiberg, Birgit Kjer, P. Kjer, Thomas Rosenberg

Journal:

Year:

1996

Language:

english

File:

PDF, 128 KB

english, 1996

35

Mitotic and meiotic instability of the CAG trinucleotide repeat in spinocerebellar ataxia type 1

Pernille Koefoed, L. Hasholt, Kirsten Fenger, Jørgen E. Nielsen, Hans Eiberg, Karsten Buschard, Sven Asger Sørensen

Journal:

Year:

1998

Language:

english

File:

PDF, 64 KB

english, 1998

36

A frameshift mutation in exon

Dawn L. Thiselton, Christiane Alexander, Alex Morris, Simon Brooks, Thomas Rosenberg, Hans Eiberg, Birgit Kjer, Poul Kjer, Shomi S. Bhattacharya, Marcela Votruba

Journal:

Year:

2001

Language:

english

File:

PDF, 89 KB

english, 2001

37

Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potential

Peter Bross, Zhijie Li, Jakob Hansen, Jens Jacob Hansen, Marit Nyholm Nielsen, Thomas Juhl Corydon, Costa Georgopoulos, Debbie Ang, Jytte Banner Lundemose, Klary Niezen-Koning, Hans Eiberg, Huanming Y

Journal:

Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 256 KB

english, 2007

38

Autozygosity mapping of a large consanguineous Pakistani family reveals a novel non-syndromic autosomal recessive mental retardation locus on 11p15-tel

Shoaib ur Rehman, Shahid Mahmood Baig, Hans Eiberg, Sijad ur Rehman, Ilyas Ahmad, Naveed Altaf Malik, Niels Tommerup, Lars Hansen

Journal:

Year:

2011

Language:

english

File:

PDF, 327 KB

english, 2011

39

A high frequent BRCA1 founder mutation identified in the Greenlandic population

Theresa Larriba Harboe, Hans Eiberg, Peder Kern, Bent Ejlertsen, Lotte Nedergaard, Vera Timmermans-Wielenga, Inge-Merete Nielsen, Marie Luise Bisgaard

Journal:

Familial Cancer

Year:

2009

Language:

english

File:

PDF, 241 KB

english, 2009

40

Screening for Y microdeletions in men with testicular cancer and undescended testis

Pinar Bor, Johnny Hindkjær, Steen Kølvraa, Philip Rossen, Hans von der Maase, Troels Munch Jørgensen, Viggo Tønning Sørensen, Hans Eiberg, Hans Jakob Ingerslev

Journal:

Journal of Assisted Reproduction and Genetics

Year:

2006

Language:

english

File:

PDF, 278 KB

english, 2006

41

Autosomal inheritance of diabetes in two families characterized by obesity and a novel H241Q mutation in NEUROD1

Lucie Gonsorčíková, Štěpánka Průhová, Ondrej Cinek, Jakob Ek, Terezie Pelikánová, Torben Jørgensen, Hans Eiberg, Oluf Pedersen, Torben Hansen, Jan Lebl

Journal:

Pediatric Diabetes

Year:

2008

Language:

english

File:

PDF, 97 KB

english, 2008

42

Hereditary phenotypes in nocturnal enuresis

Henriette L. Schaumburg, Ulla Kapilin, Christa Blåsvær, Hans Eiberg, Alexander Von Gontard, Jens Christian Djurhuus, Søren Rittig

Journal:

BJU International

Year:

2008

Language:

english

File:

PDF, 169 KB

english, 2008

43

The influence of parental history of diabetes and offspring birthweight on offspring glucose metabolism in adulthood

JEANNET LAUENBORG, MIE KW JØRGENSEN, PETER DAMM, ATHELINE MAJOR-PEDERSEN, HANS EIBERG, SØREN URHAMMER, OLUF PEDERSEN, TORBEN HANSEN

Journal:

Acta Obstetricia et Gynecologica Scandinavica

Year:

2011

Language:

english

File:

PDF, 202 KB

english, 2011

44

Cytoplasmic expression of E-cadherin and β-Catenin correlated with LOH and hypermethylation of the APC gene in oral squamous cell carcinomas

Shan Gao, Hans Eiberg, Annelise Krogdahl, Chung-Ji Liu, Jens Ahm Sørensen

Journal:

Journal of Oral Pathology & Medicine

Year:

2005

Language:

english

File:

PDF, 306 KB

english, 2005

45

LOH at chromosome 9q34.3 and the Notch1 gene methylation are less involved in oral squamous cell carcinomas

Shan Gao, Annelise Krogdahl, Hans Eiberg, Chung-Ji Liu, Jens Ahm Sørensen

Journal:

Journal of Oral Pathology & Medicine

Year:

2007

Language:

english

File:

PDF, 615 KB

english, 2007

46

A novel nonsense mutation in PAX9 is associated with marked variability in number of missing teeth

Lars Hansen, Sven Kreiborg, Henrik Jarlov, Erik Niebuhr, Hans Eiberg

Journal:

European Journal of Oral Sciences

Year:

2007

Language:

english

File:

PDF, 526 KB

english, 2007

47

New selective Giemsa technique for human chromosomes, Cd staining

Journal:

Year:

1974

File:

PDF, 138 KB

1974

48

Localization of cystic fibrosis locus to human chromosome 7cen–q22

Wainwright, Brandon J., Scambler, Peter J., Schmidtke, Jorg, Watson, Eila A., Law, Hai-Yang, Farrall, Martin, Cooke, Howard J., Eiberg, Hans, Williamson, Robert

Journal:

Year:

1985

File:

PDF, 240 KB

1985

49

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

Farooq, Muhammad, Troelsen, Jesper T, Boyd, Mette, Eiberg, Hans, Hansen, Lars, Hussain, Muhammad Sajid, Rehman, Shoaib ur, Azhar, Aysha, Ali, Amjad, Bakhtiar, Syeda Marriam

Journal:

European Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 295 KB

english, 2010

50

Assignment of dominant inherited nocturnal enuresis (ENUR1) to chromosome 13q

Eiberg, Hans, Berendt, Ida, Mohr, Jan

Journal:

Nature Genetics

Year:

1995

File:

PDF, 362 KB

1995

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