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Lars Hansen

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M Sajid Hussain; Niels Tommerup; S M Baig; K W Kjaer; A A Noegel; I Anjum; Hans Eiberg; M Farooq; E Janzen; S Marriam Bakhtiar; P Nürnberg; M Reza Toliat; Lars Hansen
Genetic heterogeneity in Pakistani microcephaly families.
Lars Hansen; Taroh Kinoshita; Yusuke Maeda; Yuan Mang; Safia Muhammad; Yoshiko Murakami; Markus M Nöthen; André Reis; Stefanie Schaffer; Hasan Tawamie; Niels Tommerup; Shoaib ur Rehman; Michael Aigner; Shahid Mahmood Baig; Mads Bak; Eric P Bennett; Rebecca Buchert; Rami Abou Jamra
Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability.
Lars Hansen; Thomas Rosenberg
Author response: Nonspecific PCR amplification of CRYBB2-pseudogene leads to misconception of natural variation as mutation.

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All Publications

2013: M Sajid Hussain; Niels Tommerup; S M Baig; K W Kjaer; A A Noegel; I Anjum; Hans Eiberg; M Farooq; E Janzen; S Marriam Bakhtiar; P Nürnberg; M Reza Toliat; Lars Hansen
Genetic heterogeneity in Pakistani microcephaly families.
Clinical genetics 2013;83(5):446-51.
2013: Lars Hansen; Taroh Kinoshita; Yusuke Maeda; Yuan Mang; Safia Muhammad; Yoshiko Murakami; Markus M Nöthen; André Reis; Stefanie Schaffer; Hasan Tawamie; Niels Tommerup; Shoaib ur Rehman; Michael Aigner; Shahid Mahmood Baig; Mads Bak; Eric P Bennett; Rebecca Buchert; Rami Abou Jamra
Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability.
American journal of human genetics 2013;92(4):575-83.
2012: Lars Hansen; Thomas Rosenberg
Author response: Nonspecific PCR amplification of CRYBB2-pseudogene leads to misconception of natural variation as mutation.
Investigative ophthalmology & visual science 2012;53(10):6666.
2012: Marie Louise M Andersen; Ahmed Delli; Lars Hansen; Emma Jacobssen; Ake Lernmark; Henrik B Mortensen; Sven Pörksen; Jacob Steen Petersen; Jannet Svensson; Jane Thomsen; Fariba Vaziri-Sani; Lotte B Nielsen
Association between autoantibodies to the Arginine variant of the Zinc transporter 8 (ZnT8) and stimulated C-peptide levels in Danish children and adolescents with newly diagnosed type 1 diabetes.
Pediatric diabetes 2012;13(6):454-62.
2012: Hans Eiberg; Lars Friberg; Lars Hansen; Lena Elisabeth Hjermind; L Korbo; I M Nielsen; O R Olsen; L H Pinborg; K Svenstrup; S Bech; Jørgen E Nielsen
Novel mutation in ATP13A2 widens the spectrum of Kufor-Rakeb syndrome (PARK9).
Clinical genetics 2012;82(3):256-63.
2012: Linda P Jakobsen; L L Klitten; Y Mang; Rikke Steensbjerre Møller; P Pfeiffer; M Andersen; M Bak; Hans Eiberg; Lars Hansen; Niels Tommerup
Genetic studies in congenital anterior midline cervical cleft.
American journal of medical genetics. Part A 2012;158A(8):2021-6.
2012: Anne Kaas; Henrik B Mortensen; Lotte B Nielsen; Jacob Steen Petersen; Kenneth J Robertson; Marie Louise Max Andersen; Karsten Buschard; Carine de Beaufort; Siri Fredheim; Lars Hansen; Philip Hougaard
Proinsulin, GLP-1, and glucagon are associated with partial remission in children and adolescents with newly diagnosed type 1 diabetes.
Pediatric diabetes 2012;13(1):51-8.
2012: Lotte B Nielsen; Flemming Pociot; Kaspar Sørensen; Cheng Wang; Chen-Yu Zhang; Marie-Louise M Andersen; Claus H Bang-Berthelsen; Lars Hansen; Philip Hougaard; Anders Juul; Henrik B Mortensen
Circulating levels of microRNA from children with newly diagnosed type 1 diabetes and healthy controls: evidence that miR-25 associates to residual beta-cell function and glycaemic control during disease progression.
Experimental diabetes research 2012;2012():896362.
2011: Lotte B Nielsen; Flemming Pociot; Sven Pörksen; Jannet Svensson; Fariba Vaziri-Sani; Marie-Louise M Andersen; Regine Bergholdt; Luis Castaño; Carine de Beaufort; Lars Hansen; Philip Hougaard; Ake Lernmark; Henrik B Mortensen
Relationship between ZnT8Ab, the SLC30A8 gene and disease progression in children with newly diagnosed type 1 diabetes.
Autoimmunity 2011;44(8):616-23.
2011: Shoaib ur Rehman; Sijad ur Rehman; Naveed Altaf Malik; Niels Tommerup; Ilyas Ahmad; Shahid Mahmood Baig; Hans Eiberg; Lars Hansen
Autozygosity mapping of a large consanguineous Pakistani family reveals a novel non-syndromic autosomal recessive mental retardation locus on 11p15-tel.
Neurogenetics 2011;12(3):247-51.
2011: Nanna Dahl Rendtorff; Marianne Lodahl; Houda Boulahbel; Ida R Johansen; Arti Pandya; Katherine O Welch; Virginia W Norris; Kathleen S Arnos; Maria Bitner-Glindzicz; Sarah B Emery; Marilyn B Mets; Toril Fagerheim; Kristina Eriksson; Lars Hansen; Helene Bruhn; Claes Möller; Sture Lindholm; Stefan Ensgaard; Marci M Lesperance; Lisbeth Tranebjaerg
Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment.
American journal of medical genetics. Part A 2011;155A(6):1298-313.
2011: Linda P Jakobsen; Merete Bugge; Reinhard Ullmann; Charlotte K Schjerling; Rehannah Borup; Lars Hansen; Hans Eiberg; Niels Tommerup
500K SNP array analyses in blood and saliva showed no differences in a pair of monozygotic twins discordant for cleft lip.
American journal of medical genetics. Part A 2011;155A(3):652-5.
2011: Lars Hansen; A K Riis; Asli N Silahtaroglu; Hanne Hove; E Lauridsen; Hans Eiberg; Sven Kreiborg
RUNX2 analysis of Danish cleidocranial dysplasia families.
Clinical genetics 2011;79(3):254-63.
2011: Siri Fredheim; Lars Hansen; Torben Hansen; Henrik Bindesbøl Mortensen; Oluf Borbye Pedersen; Sven Pørksen; Jannet Svensson; Fabrizio Barbetti; Lotte Brøndum Nielsen
Intrafamilial Variability of Early-Onset Diabetes due to an INS Mutation.
Case reports in genetics 2011;2011():258978.
2011: Camilla Helene Sandholt; Marie Aare Vestmar; Daniel Witte; Katrine Almind; Dorthe Sadowa Bille; Anders Borglykke; Lars Hansen; Torben Jørgensen; Torsten Lauritzen; Oluf Pedersen; Annelli Sandbaek; Torben Hansen
Studies of metabolic phenotypic correlates of 15 obesity associated gene variants.
PloS one 2011;6(9):e23531.
2011: Lotte B Nielsen; Sven Pörksen; Marie Louise M Andersen; Siri Fredheim; Jannet Svensson; Philip Hougaard; Maurizio Vanelli; Jan Åman; Henrik B Mortensen; Lars Hansen
The PTPN22 C1858T gene variant is associated with proinsulin in new-onset type 1 diabetes.
BMC medical genetics 2011;12():41.
2010: Muhammad Farooq; Jesper T Troelsen; Mette Boyd; Hans Eiberg; Lars Hansen; Muhammad Sajid Hussain; Shoaib ur Rehman; Aysha Azhar; Amjad Ali; Syeda Marriam Bakhtiar; Niels Tommerup; Shahid Mahmood Baig; Klaus W Kjaer
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.
European journal of human genetics : EJHG 2010;18(6):733-6.
2010: Iram Anjum; Hans Eiberg; Shahid Mahmood Baig; Niels Tommerup; Lars Hansen
A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family.
Molecular vision 2010;16():549-55.
2009: Lars Hansen; Annemette Mikkelsen; Gudrun Nürnberg; Peter Nürnberg; Iram Anjum; Hans Eiberg; Thomas Rosenberg
Comprehensive mutational screening in a cohort of Danish families with hereditary congenital cataract.
Investigative ophthalmology & visual science 2009;50(7):3291-303.
2009: Jakob Albrethsen; Steen Gammeltoft; Lars Hansen; Anne Kaas; Mirjana Kocova; Eugen Schönle; Peter Swift; Henrik Bindesbøl Mortensen
Evaluation of a type 1 diabetes serum cohort by SELDI-TOF MS protein profiling.
Proteomics. Clinical applications 2009;3(3):383-93.
2008: Hans Eiberg; Jesper T Troelsen; Mette Nielsen; Annemette Mikkelsen; Jonas Mengel-From; Klaus W Kjaer; Lars Hansen
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.
Human genetics 2008;123(2):177-87.
2007: Lars Hansen; Wenliang Yao; Hans Eiberg; Klaus Wilbrandt Kjaer; Kirsten Baggesen; J Fielding Hejtmancik; Thomas Rosenberg
Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8.
Investigative ophthalmology & visual science 2007;48(9):3937-44.
2007: Lars Hansen; Sven Kreiborg; Henrik Jarlov; Erik Niebuhr; Hans Eiberg
A novel nonsense mutation in PAX9 is associated with marked variability in number of missing teeth.
European journal of oral sciences 2007;115(4):330-3.
2007: Lars Hansen; Hans Eiberg; Thomas Rosenberg
Novel MAF mutation in a family with congenital cataract-microcornea syndrome.
Molecular vision 2007;13():2019-22.
2006: Hans Eiberg; Lars Hansen; Birgit Kjer; Torben Hansen; Oluf Pedersen; Michael Bille; Thomas Rosenberg; Lisbeth Tranebjaerg
Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.
Journal of medical genetics 2006;43(5):435-40.
2006: Klaus Wilbrandt Kjaer; Hans Eiberg; Lars Hansen; C B van der Hagen; K Rosendahl; Niels Tommerup; Stefan Mundlos
A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2.
Journal of medical genetics 2006;43(3):225-31.
2006: Lars Hansen; Wenliang Yao; Hans Eiberg; Mikkel Funding; Ruth Riise; Klaus Wilbrandt Kjaer; J Fielding Hejtmancik; Thomas Rosenberg
The congenital "ant-egg" cataract phenotype is caused by a missense mutation in connexin46.
Molecular vision 2006;12():1033-9.
2005: Lars Hansen; Hans Eiberg; Timothy Barrett; Toke Bek; Per Kjaersgaard; Lisbeth Tranebjaerg; Thomas Rosenberg
Mutation analysis of the WFS1 gene in seven Danish Wolfram syndrome families; four new mutations identified.
European journal of human genetics : EJHG 2005;13(12):1275-84.
2005: Klaus Wilbrandt Kjaer; Lars Hansen; Hans Eiberg; Algirdas Utkus; Lene Theil Skovgaard; Pernille Leicht; John M Opitz; Niels Tommerup
A 72-year-old Danish puzzle resolved--comparative analysis of phenotypes in families with different-sized HOXD13 polyalanine expansions.
American journal of medical genetics. Part A 2005;138(4):328-39.
2005: Klaus Wilbrandt Kjaer; Lars Hansen; Hans Eiberg; Knud Stenild Christensen; John M Opitz; Niels Tommerup
Male-to-male transmission in Laurin-Sandrow syndrome and exclusion of RARB and RARG.
American journal of medical genetics. Part A 2005;137(2):148-52.
2005: Klaus Wilbrandt Kjaer; Lars Hansen; Georg C Schwabe; A P Marques-de-Faria; Hans Eiberg; Stefan Mundlos; Niels Tommerup; Thomas Rosenberg
Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome).
Journal of medical genetics 2005;42(4):292-8.
2005: Qingfa Wu; Erik Niebuhr; Huanming Yang; Lars Hansen
Determination of the 'critical region' for cat-like cry of Cri-du-chat syndrome and analysis of candidate genes by quantitative PCR.
European journal of human genetics : EJHG 2005;13(4):475-85.
2005: Hans Eiberg; Lars Hansen; Claus Hansen; Jan Mohr; Peter Stubbe Teglbjaerg; Klaus Wilbrandt Kjaer
Mapping of hereditary trichilemmal cyst (TRICY1) to chromosome 3p24-p21.2 and exclusion of beta-CATENIN and MLH1.
American journal of medical genetics. Part A 2005;133A(1):44-7.
2004: Mads Bak; Claus Hansen; Karen Friis Henriksen; Lars Hansen; Henning Pakkenberg; Hans Eiberg; Niels Tommerup
Mutation analysis of the Sonic hedgehog promoter and putative enhancer elements in Parkinson's disease patients.
Brain research. Molecular brain research 2004;126(2):207-11.
2004: Klaus Wilbrandt Kjaer; Lars Hansen; Hans Eiberg; Pernille Leicht; John M Opitz; Niels Tommerup
Novel Connexin 43 (GJA1) mutation causes oculo-dento-digital dysplasia with curly hair.
American journal of medical genetics. Part A 2004;127A(2):152-7.