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Anders Børglum

Research Profile

Physiology

Genes & Molecular Sequences

Single Nucleotide Polymorphism

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Henriette N Buttenschøn; Søren Christoffersen; Tracey J Flint; Leslie Foldager; Nikolaj F Hansen; Ingrid B Kristensen; Preben B Mortensen; Ping Qin; Anders D Børglum; Ole Mors
An association study of suicide and candidate genes in the serotonergic system.
T Harsløf; L B Husted; Marianne Andersen; Anders D Børglum; Kim Brixen; M Frost; Leif Mosekilde; Torben Leo Nielsen; Mette Nyegaard; Lars Rejnmark; Bente Langdahl
Polymorphisms of muscle genes are associated with bone mass and incident osteoporotic fractures in Caucasians.
Peter Saetre; Lars Terenius; Maria Vares; Thomas Werge; Ingrid Agartz; Ole A Andreassen; Anders D Børglum; Jakob Grove; Ole Mors; Erik G Jönsson
Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age at onset of schizophrenia: no consistent evidence for an association in the Nordic population.

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2013: Henriette N Buttenschøn; Søren Christoffersen; Tracey J Flint; Leslie Foldager; Nikolaj F Hansen; Ingrid B Kristensen; Preben B Mortensen; Ping Qin; Anders D Børglum; Ole Mors
An association study of suicide and candidate genes in the serotonergic system.
Journal of affective disorders 2013;148(2-3):291-8.
2013: T Harsløf; L B Husted; Marianne Andersen; Anders D Børglum; Kim Brixen; M Frost; Leif Mosekilde; Torben Leo Nielsen; Mette Nyegaard; Lars Rejnmark; Bente Langdahl
Polymorphisms of muscle genes are associated with bone mass and incident osteoporotic fractures in Caucasians.
Calcified tissue international 2013;92(5):467-76.
2012: Peter Saetre; Lars Terenius; Maria Vares; Thomas Werge; Ingrid Agartz; Ole A Andreassen; Anders D Børglum; Jakob Grove; Ole Mors; Erik G Jönsson
Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age at onset of schizophrenia: no consistent evidence for an association in the Nordic population.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012;159B(8):981-6.
2012: Mette Nyegaard; Michael T Overgaard; Mads T Søndergaard; Marta Vranas; göran wettrell; A John Camm; Michael Christiansen; Inger Fosdal; Paula L Hedley; Lasse L Hildebrandt; Jacob Lund; Elijah R Behr; Anders D Børglum
Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death.
American journal of human genetics 2012;91(4):703-12.
2012: Morten Petersen; Steen Stender; Christian Torp-Pedersen; Shoaib Afzal; Jon T Andersen; Anders D Børglum; Kasper Broedbaek; Espen Jimenez-Solem; Lars Køber; Mette Nyegaard; Henrik E Poulsen
Effect of specific ADRB1/ADRB2/AGT genotype combinations on the association between survival and carvedilol treatment in chronic heart failure: a substudy of the ECHOS trial.
Pharmacogenetics and genomics 2012;22(10):709-15.
2012: Betina Elfving; Leslie Foldager; Matias B Grynderup; Linda Kaerlev; Henrik A Kolstad; Sigurd Mikkelsen; Pia H P Poulsen; Jane F Thomsen; Gregers Wegener; Åse M Hansen; Johan H Andersen; Anders D Børglum; Henriette N Buttenschøn; Ole Mors
Depression, the Val66Met polymorphism, age, and gender influence the serum BDNF level.
Journal of psychiatric research 2012;46(9):1118-25.
2012: Jane H Christensen; Thomas J Corydon; Betina Elfving; Tue Fryland; Ole Mors; Heidi K Müller; Anders Lade Nielsen; Mette Nyegaard; Gregers Wegener; Anders D Børglum
The Schizophrenia and Bipolar Disorder associated BRD1 gene is regulated upon chronic restraint stress.
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2012;22(9):651-6.
2012: Carsten Bøcker Pedersen; M S Pedersen; Esben Agerbo; Anders D Børglum; D Demontis; M V Hollegaard; D M Hougaard; Ole Mors; Preben Bo Mortensen; Elizabeth Cantor-Graae
Risk of schizophrenia in relation to parental origin and genome-wide divergence.
Psychological medicine 2012;42(7):1515-21.
2012: Mette Nyegaard; Karina Meden Sørensen; Britta Boserup Thestrup; Thomas Werge; Robert H Yolken; Ditte Demontis; Thomas Hansen; Anne Hedemand; David Michael Hougaard; Ole Mors; Preben Bo Mortensen; Anders D Børglum
No association of polymorphisms in human endogenous retrovirus K18 and CD48 with schizophrenia.
Psychiatric genetics 2012;22(3):146-8.
2012: Michael S Pedersen; Esben Agerbo; Michael E Benros; Anders D Børglum; Preben B Mortensen
Schizophrenia in patients with atopic disorders with particular emphasis on asthma: a Danish population-based study.
Schizophrenia research 2012;138(1):58-62.
2012: Tue Fryland; Ole Mors; Gregers Wegener; Jane H Christensen; Betina Elfving; Anders D Børglum
Electroconvulsive seizures regulates the Brd1 gene in the frontal cortex and hippocampus of the adult rat.
Neuroscience letters 2012;516(1):110-3.
2012: Ditte Demontis; Thomas Hansen; Anne Hedemand; Ole Mors; Mette Nyegaard; Jacob Severinsen; Thomas Werge; Jane H Christensen; Anders D Børglum
The gene encoding the melanin-concentrating hormone receptor 1 is associated with schizophrenia in a Danish case-control sample.
Psychiatric genetics 2012;22(2):62-9.
2011: Ditte Demontis; Tracey J Flint; Jakob Grove; Anne Hedemand; David M Hougaard; Ole Mors; Merete Nordentoft; Mette Nyegaard; Carsten B Pedersen; Karina M Sørensen; Thomas Werge; Robert H Yolken; Anders D Børglum; Henriette N Buttenschøn; Preben Bo Mortensen
Association of GRIN1 and GRIN2A-D with schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011;156B(8):913-22.
2011: Dorte Haubek; Anders D Børglum; Hans Gjørup; Lillian G Jensen; Inger Juncker; Mette Nyegaard; Sven Poulsen; Jens M Hertz
Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutation.
International journal of paediatric dentistry / the British Paedodontic Society [and] the International Association of Dentistry for Children 2011;21(6):407-12.
2011: Per Qvist; Muhammad J Hassan; Pablo Huertas; Stephen P Jackson; Sonia Jimeno; Mette Nyegaard; Anders D Børglum
CtIP Mutations Cause Seckel and Jawad Syndromes.
PLoS genetics 2011;7(10):e1002310.
2011: T Harsløf; L B Husted; J-E B Jensen; Anders D Børglum; Kim Brixen; Mette Carstens; Pia Eiken; Leif Mosekilde; Mette Nyegaard; Lars Rejnmark; Liselotte Stenkjaer; Bente Langdahl
Polymorphisms in the ALOX12 gene and osteoporosis.
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2011;22(8):2249-59.
2011: Tune H Pers; Shaun Purcell; Thomas Werge; Christopher T Workman; Ole A Andreassen; Anders D Børglum; Henrik Dam; Srdjan Djurovic; Piotr Dworzynski; Manuel A Ferreira; Tracey J Flint; Niclas Tue Hansen; Torben Hansen; Pernille Koefoed; Irene Kouskoumvekaki; Kasper Lage; Ingrid Melle; Erling Mellerup; Martin Lee Miller; Ole Mors; Søren Brunak
Meta-analysis of heterogeneous data sources for genome-scale identification of risk genes in complex phenotypes.
Genetic epidemiology 2011;35(5):318-32.
2011: H N Buttenschøn; A S Kristensen; H N Buch; J H Andersen; J P Bonde; M Grynderup; A M Hansen; H Kolstad; A Kaergaard; L Kaerlev; S Mikkelsen; J F Thomsen; P Koefoed; Erhardt Angelika; D P D Woldbye; Anders D Børglum; Ole Mors
The norepinephrine transporter gene is a candidate gene for panic disorder.
Journal of neural transmission (Vienna, Austria : 1996) 2011;118(6):969-76.
2011: Jessica E Van Schijndel; Martine Van Zweeden; Thomas Werge; Rolf Adolfsson; Ole A Andreassen; Anders D Børglum; Sven Cichon; Stephan Claes; marc de hert; Jurgen Del-Favero; Srdjan Djurovic; Thomas Hansen; Pekka Kallunki; Ole Mors; Preben B Mortensen; Merete Nordentoft; Karl-Fredrik Norrback; Markus M Nöthen; Mette Nyegaard; Jan Torleif Pedersen; Marcella Rietschel; Karina Meden Sørensen; Karen van Loo; Gerard J M Martens
Dual association of a TRKA polymorphism with schizophrenia.
Psychiatric genetics 2011;21(3):125-31.
2011: Morten Petersen; Jon T Andersen; Brian R Hjelvang; Kasper Broedbaek; Shoaib Afzal; Mette Nyegaard; Anders D Børglum; Steen Stender; Lars Køber; Christian Torp-Pedersen; Henrik E Poulsen
Association of beta-adrenergic receptor polymorphisms and mortality in carvedilol-treated chronic heart-failure patients.
British journal of clinical pharmacology 2011;71(4):556-65.
2011: Mads V Hollegaard; Eskil Kreiner-Møller; Ole Mors; Preben B Mortensen; Mette Nørgaard; Bent Nørgaard-Pedersen; Henrik T Sørensen; Torben F Orntoft; Thomas L Benfield; Hans Bisgaard; Klaus Bønnelykke; Anders D Børglum; Ditte Demontis; Jonas Grauholm; Jakob Grove; Zitta B Harboe; David M Hougaard
Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source.
BMC genetics 2011;12():58.
2011: Bjørn A Nexø; Tove Christensen; Jette Frederiksen; Anné Møller-Larsen; Annette Oturai; Palle Villesen; Bettina Hansen; Kari K Nissen; Magdalena J Laska; Trine S Petersen; Sandra Bonnesen; Anne Hedemand; Tingting Wu; Xinjie Wang; Xiuqing Zhang; Tomasz Brudek; Romana Maric; Helle B Søndergaard; Finn Sellebjerg; Klaus Brusgaard; Anders L Kjeldbjerg; Henrik B Rasmussen; Anders L Nielsen; Mette Nyegaard; Thor Petersen; Anders D Børglum; Finn Skou Pedersen
The etiology of multiple sclerosis: genetic evidence for the involvement of the human endogenous retrovirus HERV-Fc1.
PloS one 2011;6(2):e16652.
2010: Preben B Mortensen; Carsten Bøcker Pedersen; David M Hougaard; Bent Nørgaard-Petersen; Ole Mors; Anders D Børglum; Robert H Yolken
A Danish National Birth Cohort study of maternal HSV-2 antibodies as a risk factor for schizophrenia in their offspring.
Schizophrenia research 2010;122(1-3):257-63.
2010: Henriette Nørmølle Buttenschøn; Henriette Nørmølle Buttenchøn; Leslie Foldager; Tracey J Flint; Inger Marie L Olsen; Thomas Deleuran; Mette Nyegaard; Mette M Hansen; Pekka Kallunki; Kenneth Vielsted Christensen; Douglas H Blackwood; Walter J Muir; Steen E Straarup; Thomas D Als; Merete Nordentoft; Anders D Børglum; Ole Mors
Support for a bipolar affective disorder susceptibility locus on chromosome 12q24.3.
Psychiatric genetics 2010;20(3):93-101.
2010: Mette Nyegaard; Jacob E Severinsen; Thomas D Als; Anne Hedemand; Steen Straarup; Merete Nordentoft; Andrew McQuillin; Nicholas Bass; Jacob Lawrence; Srinivasa Thirumalai; Ana C P Pereira; Radhika Kandaswamy; Gregory J Lydall; Pamela Sklar; Edward Scolnick; Shaun Purcell; David Curtis; Hugh M D Gurling; Preben B Mortensen; Ole Mors; Anders D Børglum
Support of association between BRD1 and both schizophrenia and bipolar affective disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010;153B(2):582-91.
2010: Mette Nyegaard; D Demontis; L Foldager; A Hedemand; T J Flint; K M Sørensen; P S Andersen; M Nordentoft; T Werge; C B Pedersen; D M Hougaard; P B Mortensen; Ole Mors; Anders D Børglum
CACNA1C (rs1006737) is associated with schizophrenia.
Molecular psychiatry 2010;15(2):119-21.
2010: Jenny Blechingberg; Ida Elisabeth Holm; Marianne G Johansen; Anders D Børglum; Anders Lade Nielsen
Aromatic l-amino acid decarboxylase expression profiling and isoform detection in the developing porcine brain.
Brain research 2010;1308():1-13.
2009: Carsten R Bjarkam; Thomas J Corydon; Inger Marie L Olsen; Jonatan Pallesen; Mette Nyegaard; Tue Fryland; Ole Mors; Anders D Børglum
Further immunohistochemical characterization of BRD1 a new susceptibility gene for schizophrenia and bipolar affective disorder.
Brain structure & function 2009;214(1):37-47.
2009: Ulla Christensen; Steffen Møller-Larsen; Mette Nyegaard; Annette Haagerup; Anne Hedemand; Charlotte Brasch-Andersen; Torben A Kruse; Thomas J Corydon; Mette Deleuran; Anders D Børglum
Linkage of atopic dermatitis to chromosomes 4q22, 3p24 and 3q21.
Human genetics 2009;126(4):549-57.
2009: Ditte Demontis; Thomas G Jensen; Anders D Børglum
[Genetic variation studies a breakthrough in the understanding of many common diseases].
Ugeskrift for laeger 2009;171(13):1096.
2008: S Møller-Larsen; Mette Nyegaard; Annette Haagerup; Jørgen Vestbo; Torben A Kruse; Anders D Børglum
Association analysis identifies TLR7 and TLR8 as novel risk genes in asthma and related disorders.
Thorax 2008;63(12):1064-9.
2008: Bjørn A Nexø; Ulla Vogel; Anja Olsen; Mette Nyegaard; Zuzanna Bukowy; Eszter Rockenbauer; Xiuqing Zhang; Cemile Koca; Mette Mains; Bettina Hansen; Anne Hedemand; Anette Kjeldgaard; Magdalena J Laska; Ole Raaschou-Nielsen; Søren Cold; Kim Overvad; Anne Tjønneland; Lars Bolund; Anders D Børglum
Linkage disequilibrium mapping of a breast cancer susceptibility locus near RAI/PPP1R13L/iASPP.
BMC medical genetics 2008;9():56.
2007: Thomas J Corydon; Annette Haagerup; Thomas G Jensen; Helle Glud Binderup; Mikkel S Petersen; Keld Kaltoft; Jørgen Vestbo; Torben A Kruse; Anders D Børglum
A functional CD86 polymorphism associated with asthma and related allergic disorders.
Journal of medical genetics 2007;44(8):509-15.
2007: Anders D Børglum; Cristiano Vernesi; Peter Koch Jensen; Bo Madsen; Annette Haagerup; Guido Barbujani
No signature of Y chromosomal resemblance between possible descendants of the Cimbri in Denmark and Northern Italy.
American journal of physical anthropology 2007;132(2):278-84.
2006: B Marcheco-Teruel; Tracey J Flint; Friedrik P Wikman; M Torralbas; L González; L Blanco; Q Tan; Henrik Ewald; Torben F Orntoft; Torben A Kruse; Anders D Børglum; Ole Mors
A genome-wide linkage search for bipolar disorder susceptibility loci in a large and complex pedigree from the eastern part of Cuba.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006;141B(8):833-43.
2006: J E Severinsen; Carsten R Bjarkam; S Kiaer-Larsen; I M Olsen; Morten Muhlig Nielsen; J Blechingberg; Anders Lade Nielsen; Ida E Holm; Leslie Foldager; B D Young; Walter J Muir; D H R Blackwood; Thomas J Corydon; Ole Mors; Anders D Børglum
Evidence implicating BRD1 with brain development and susceptibility to both schizophrenia and bipolar affective disorder.
Molecular psychiatry 2006;11(12):1126-38.
2006: Charlotte Brasch-Andersen; Qihua Tan; Anders D Børglum; Annette Haagerup; T R Larsen; Jørgen Vestbo; Torben A Kruse
Significant linkage to chromosome 12q24.32-q24.33 and identification of SFRS8 as a possible asthma susceptibility gene.
Thorax 2006;61(10):874-9.
2006: J E Severinsen; Thomas D Als; Helle Glud Binderup; Torben A Kruse; August Wang; Maria Vang; Walter J Muir; D H R Blackwood; Ole Mors; Anders D Børglum
Association analyses suggest GPR24 as a shared susceptibility gene for bipolar affective disorder and schizophrenia.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006;141B(5):524-33.
2006: Thomas D Als; Tove H Jorgensen; Anders D Børglum; Peter A Petersen; Ole Mors; August Wang
Highly discrepant proportions of female and male Scandinavian and British Isles ancestry within the isolated population of the Faroe Islands.
European journal of human genetics : EJHG 2006;14(4):497-504.
2006: Charlotte Brasch-Andersen; Annette Haagerup; Anders D Børglum; Jørgen Vestbo; Torben A Kruse
Highly significant linkage to chromosome 3q13.31 for rhinitis and related allergic diseases.
Journal of medical genetics 2006;43(3):e10.
2006: Ulla Christensen; Annette Haagerup; Helle Glud Binderup; Jørgen Vestbo; Torben A Kruse; Anders D Børglum
Family based association analysis of the IL2 and IL15 genes in allergic disorders.
European journal of human genetics : EJHG 2006;14(2):227-35.
2005: Niels Peter Ole Mors; Anders D Børglum
[Status of and perspectives on psychiatric genomic medicine].
Ugeskrift for laeger 2005;167(20):2191-3.
2005: Søren Vang; Thomas J Corydon; Anders D Børglum; Melissa D Scott; Judith Frydman; Jens Mogensen; Niels Gregersen; Peter Bross
Actin mutations in hypertrophic and dilated cardiomyopathy cause inefficient protein folding and perturbed filament formation.
The FEBS journal 2005;272(8):2037-49.
2004: Gemma K Alderton; Hans Joenje; Raymonda Varon; Anders D Børglum; Penny A Jeggo; Mark O'Driscoll
Seckel syndrome exhibits cellular features demonstrating defects in the ATR-signalling pathway.
Human molecular genetics 2004;13(24):3127-38.
2004: Tove H Jorgensen; Henriette N Buttenschön; August Wang; Thomas D Als; Anders D Børglum; Henrik Ewald
The origin of the isolated population of the Faroe Islands investigated using Y chromosomal markers.
Human genetics 2004;115(1):19-28.
2004: Jens Mogensen; A Perrot; Paal Skytt Andersen; Ole Havndrup; Ib C Klausen; Michael Christiansen; Peter Bross; Henrik Egeblad; Henning Bundgaard; K J Osterziel; Georg Haltern; Harald Lapp; Petra Reinecke; Niels Gregersen; Anders D Børglum
Clinical and genetic characteristics of alpha cardiac actin gene mutations in hypertrophic cardiomyopathy.
Journal of medical genetics 2004;41(1):e10.
2004: Annette Haagerup; Anders D Børglum; Helle Glud Binderup; Torben A Kruse
Fine-scale mapping of type I allergy candidate loci suggests central susceptibility genes on chromosomes 3q, 4q and Xp.
Allergy 2004;59(1):88-94.
2003: Anders D Børglum; G Kirov; N Craddock; Ole Mors; Walter Muir; V Murray; I McKee; David A Collier; Henrik Ewald; Michael J Owen; D H R Blackwood; Torben A Kruse
Possible parent-of-origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;117B(1):18-22.
2003: Jens Jacob Hansen; Peter Bross; Majken Westergaard; Marit Nyholm Nielsen; Hans Eiberg; Anders D Børglum; Jens Mogensen; Karsten Kristiansen; Lars Bolund; Niels Gregersen
Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter.
Human genetics 2003;112(1):71-7.
2002: Marlene B Lauritsen; Anders D Børglum; Catalina Betancur; Anne Philippe; Torben A Kruse; Marion Leboyer; Henrik Ewald
Investigation of two variants in the DOPA decarboxylase gene in patients with autism.
American journal of medical genetics 2002;114(4):466-70.
2002: Jurgen Del-Favero; Sofie Van Gestel; Anders D Børglum; Walter Muir; Henrik Ewald; Ole Mors; Sladana Ivezic; Lilijana Oruc; Rolf Adolfsson; Douglas Blackwood; Torben Kruse; Julien Mendlewicz; Martin Schalling; Christine Van Broeckhoven
European combined analysis of the CTG18.1 and the ERDA1 CAG/CTG repeats in bipolar disorder.
European journal of human genetics : EJHG 2002;10(4):276-80.
2002: Tove H Jorgensen; Anders D Børglum; Ole Mors; August Wang; M Pinaud; Tracey J Flint; H A Dahl; Maria Vang; Torben A Kruse; Henrik Ewald
Search for common haplotypes on chromosome 22q in patients with schizophrenia or bipolar disorder from the Faroe Islands.
American journal of medical genetics 2002;114(2):245-52.
2002: Mette Nyegaard; Anders D Børglum; T G Bruun; David A Collier; Carsten Russ; Ole Mors; Henrik Ewald; Torben A Kruse
Novel polymorphisms in the somatostatin receptor 5 (SSTR5) gene associated with bipolar affective disorder.
Molecular psychiatry 2002;7(7):745-54.
2001: Paal Skytt Andersen; Ole Havndrup; Henning Bundgaard; Johanna C Moolman-Smook; Lars Larsen; Jens Mogensen; Paul A Brink; Anders D Børglum; Valerie A Corfield; Keld Kjeldsen; Jens Vuust; Michael Christiansen
Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations.
Journal of medical genetics 2001;38(12):E43.
2001: Anders D Børglum; M Hampson; T E Kjeldsen; Walter Muir; V Murray; Henrik Ewald; Ole Mors; D H R Blackwood; Torben A Kruse
Dopa decarboxylase genotypes may influence age at onset of schizophrenia.
Molecular psychiatry 2001;6(6):712-7.
2001: Anders D Børglum; Thomas Balslev; Annette Haagerup; Niels H Birkebaek; Helle Glud Binderup; Torben A Kruse; Jens Michael Hertz
A new locus for Seckel syndrome on chromosome 18p11.31-q11.2.
European journal of human genetics : EJHG 2001;9(10):753-7.
2001: Anders D Børglum; Lars Bolund
[The Human Genome Project--status and perspectives].
Ugeskrift for laeger 2001;163(36):4853-6.
2001: Jens Mogensen; Paal Skytt Andersen; U Steffensen; Michael Christiansen; Henrik Egeblad; Niels Gregersen; Anders D Børglum
Development and application of linkage analysis in genetic diagnosis of familial hypertrophic cardiomyopathy.
Journal of medical genetics 2001;38(3):193-8.
1999: Anders D Børglum; T G Bruun; T E Kjeldsen; Henrik Ewald; Ole Mors; G Kirov; Carsten Russ; B Freeman; David A Collier; Torben A Kruse
Two novel variants in the DOPA decarboxylase gene: association with bipolar affective disorder.
Molecular psychiatry 1999;4(6):545-51.
1999: Jens Mogensen; Torben A Kruse; Anders D Børglum
Refined localization of the human alpha-tropomyosin gene (TPM1) by genetic mapping.
Cytogenetics and cell genetics 1999;84(1-2):35-6.
1998: Jens Mogensen; Torben A Kruse; Anders D Børglum
Assignment of the human skeletal muscle [FC12]a-actin gene (ACTA1) to chromosome 1q42.13-->q42.2 by radiation hybrid mapping.
Cytogenetics and cell genetics 1998;83(3-4):224-5.
1997: Jens Mogensen; Torben A Kruse; Anders D Børglum
Assignment of the human cardiac troponin I gene (TNNI3) to chromosome 19q13.4 by radiation hybrid mapping.
Cytogenetics and cell genetics 1997;79(3-4):272-3.
1997: Anders D Børglum; Mette Nyegaard; A B Kvistgaard; E Mullaart; A G Uitterlinden; Jan Vijg; Torben A Kruse
Mapping of 34 minisatellite loci resolved by two-dimensional DNA typing.
Cytogenetics and cell genetics 1997;79(3-4):248-56.
1997: Anders D Børglum; Tracey J Flint; L L Hansen; Torben A Kruse
Refined localization of the pyruvate dehydrogenase E1 alpha gene (PDHA1) by linkage analysis.
Human genetics 1997;99(1):80-2.
1996: Anders D Børglum; Tracey J Flint; Niels Tommerup; J Fleckner; Just Justesen; Torben A Kruse
Assignment of the human tryptophanyl-tRNA synthetase gene (WARS) to chromosome 14q32.2 --> q32.32.
Cytogenetics and cell genetics 1996;73(1-2):99-103.
1995: Anders D Børglum; Tracey J Flint; Peder Madsen; Julio E Celis; Torben A Kruse
Refined mapping of the psoriasin gene S100A7 to chromosome 1cen-q21.
Human genetics 1995;96(5):592-6.
1995: E Mullaart; A M Verwest; Anders D Børglum; André G Uitterlinden; Gerard te Meerman; Torben A Kruse; Jan Vijg
Two-dimensional DNA typing of human pedigrees: spot pattern characterization and segregation.
Genomics 1995;29(3):641-6.
1995: Anders D Børglum; E Mullaart; A B Kvistgaard; André G Uitterlinden; Jan Vijg; Torben A Kruse
Two-dimensional DNA typing as a genetic marker system in humans.
Cytogenetics and cell genetics 1995;71(3):260-5.
1994: Jens Michael Hertz; Anders D Børglum; Carsten A Brandt; Tracey J Flint; C Bisgaard
Charcot-Marie-Tooth disease type 1A: the parental origin of a de novo 17p11.2-p12 duplication.
Clinical genetics 1994;46(4):291-4.
1992: Anders D Børglum; A Byskov; A L Roldan; Torben A Kruse
Two PstI polymorphisms for the urokinase-type plasminogen activator receptor gene (PLAUR).
Human genetics 1992;89(5):584.
1992: Anders D Børglum; A Byskov; P Ragno; A L Roldan; P Tripputi; G Cassani; K Danø; F Blasi; Lars Bolund; Torben A Kruse
Assignment of the urokinase-type plasminogen activator receptor gene (PLAUR) to chromosome 19q13.1-q13.2.
American journal of human genetics 1992;50(3):492-7.
1991: Anders D Børglum; A Byskov; M V Cubellis; Torben A Kruse
An EcoRI polymorphism for the PLAUR gene.
Nucleic acids research 1991;19(23):6661.