Lars Hansen

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	Toate	Din 2020
Referințe bibliografice	3704	1683
h-index	32	21
i10-index	39	28

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Hans EibergKøbenhavns universitetAdresă de e-mail confirmată pe sund.ku.dk
Eric P BennettNovo Nordisk A/S Biopharm ResearchAdresă de e-mail confirmată pe novonordisk.com
Niels TommerupProfessor in Medical Genetics, University of CopenhagenAdresă de e-mail confirmată pe sund.ku.dk
Henrik ClausenUniversity of CopenhagenAdresă de e-mail confirmată pe sund.ku.dk
Katrine SchjoldagerCopenhagen Center for Glycomics, University of CopenhagenAdresă de e-mail confirmată pe sund.ku.dk
Yoshiki NarimatsuUniversity of Copenhagen, Copenhagen Center for Glycomics.Adresă de e-mail confirmată pe sund.ku.dk
Sergey VakhrushevAssociate Professor, University of CopenhagenAdresă de e-mail confirmată pe sund.ku.dk
Hans H. WandallProfessor, MD, PHD, CCG, ICMM, Faculty of Health, University of CopenhagenAdresă de e-mail confirmată pe sund.ku.dk
Hiren J JoshiCopenhagen Center for Glycomics, University of CopenhagenAdresă de e-mail confirmată pe sund.ku.dk
Zhang YangNovo Nordisk A/S Cell Therapy R&D unitAdresă de e-mail confirmată pe novonordisk.com
Catharina SteentoftSpecialist, Novo NordiskAdresă de e-mail confirmată pe novonordisk.com
Jesper T. TroelsenProfessor of Medicinal Biology, Department of Science and Environment, Roskilde University, Denmark.Adresă de e-mail confirmată pe ruc.dk
Zilu YeInstitute of Systems Medicine, Chinese Academy of Medical SciencesAdresă de e-mail confirmată pe ism.pumc.edu.cn
Mads BakUniversity of CopenhagenAdresă de e-mail confirmată pe regionh.dk
Sally Dabelsteenlektor, Københavns universitetAdresă de e-mail confirmată pe sund.ku.dk
Iram AnjumBiotechnology Department, Kinnaird College for Women, LahoreAdresă de e-mail confirmată pe kinnaird.edu.pk
Prof. Dr. Muhammad FarooqDepartment of Bioinformatics & Biotechnology, Government College University FaisalabadAdresă de e-mail confirmată pe gcuf.edu.pk
Torben HansenProfessor of Metabolic Genetics, University of Copenhagen, DenmarkAdresă de e-mail confirmată pe sund.ku.dk
Oluf PedersenProfessor of Metabolic Genetics, University of CopenhagenAdresă de e-mail confirmată pe sund.ku.dk
Stefan MundlosInstitut für Medizinische Genetik und Humangenetik, CharitéAdresă de e-mail confirmată pe molgen.mpg.de

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Lars Hansen

University of Copenhagen

Adresă de e-mail confirmată pe sund.ku.dk

genetics


Titlu Sortați după descrierea bibliografică Sortați după an Sortați după titlu	Citat de Citat de	Anul
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 H Eiberg, J Troelsen, M Nielsen, A Mikkelsen, J Mengel-From, KW Kjaer, ... Human genetics 123 (2), 177-187, 2008	479	2008
Immature truncated O-glycophenotype of cancer directly induces oncogenic features P Radhakrishnan, S Dabelsteen, FB Madsen, C Francavilla, KL Kopp, ... Proceedings of the National Academy of Sciences 111 (39), E4066-E4075, 2014	331	2014
An Atlas of Human Glycosylation Pathways Enables Display of the Human Glycome by Gene Engineered Cells CH 3. Narimatsu Y, Joshi H, Nason R, Van Coillie J, Karlsson R, Sun L, Ye Z ... Mol Cell 75, 1-14, 2019	241*	2019
Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8 L Hansen, W Yao, H Eiberg, KW Kjaer, K Baggesen, JF Hejtmancik, ... Investigative ophthalmology & visual science 48 (9), 3937-3944, 2007	165	2007
Mutations in c10orf11, a melanocyte-differentiation gene, cause autosomal-recessive albinism K Grønskov, CM Dooley, E Østergaard, RN Kelsh, L Hansen, ... The American Journal of Human Genetics 92 (3), 415-421, 2013	148	2013
Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene H Eiberg, L Hansen, B Kjer, T Hansen, O Pedersen, M Bille, T Rosenberg, ... Journal of medical genetics 43 (5), 435-440, 2006	147	2006
Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome) KW Kjaer, L Hansen, GC Schwabe, AP Marques-de-Faria, H Eiberg, ... Journal of medical genetics 42 (4), 292-298, 2005	131	2005
Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment ND Rendtorff, M Lodahl, H Boulahbel, IR Johansen, A Pandya, KO Welch, ... American journal of medical genetics Part A 155 (6), 1298-1313, 2011	127	2011
Loss of function of GALNT2 lowers high-density lipoproteins in humans, nonhuman primates, and rodents SA Khetarpal, KT Schjoldager, C Christoffersen, A Raghavan, ... Cell metabolism 24 (2), 234-245, 2016	126	2016
Comprehensive mutational screening in a cohort of Danish families with hereditary congenital cataract L Hansen, A Mikkelsen, P Nürnberg, G Nürnberg, I Anjum, H Eiberg, ... Investigative ophthalmology & visual science 50 (7), 3291-3303, 2009	121	2009
Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability L Hansen, H Tawamie, Y Murakami, Y Mang, S ur Rehman, R Buchert, ... The American Journal of Human Genetics 92 (4), 575-583, 2013	118	2013
Novel Connexin 43 (GJA1) mutation causes oculo–dento–digital dysplasia with curly hair KW Kjaer, L Hansen, H Eiberg, P Leicht, JM Opitz, N Tommerup American Journal of Medical Genetics Part A 127 (2), 152-157, 2004	106	2004
Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2 B Wissinger, S Dangel, H Jagle, L Hansen, B Baumann, G Rudolph, ... Investigative Ophthalmology & Visual Science 49 (2), 751-757, 2008	99	2008
Mutation analysis of the WFS1 gene in seven Danish Wolfram syndrome families; four new mutations identified L Hansen, H Eiberg, T Barrett, T Bek, P Kjærsgaard, L Tranebjærg, ... European Journal of Human Genetics 13 (12), 1275-1284, 2005	95	2005
A validated gRNA library for CRISPR/Cas9 targeting of the human glycosyltransferase genome Y Narimatsu, HJ Joshi, Z Yang, C Gomes, YH Chen, FC Lorenzetti, ... Glycobiology 28 (5), 295-305, 2018	93	2018
Molecular basis for fibroblast growth factor 23 O-glycosylation by GalNAc-T3. HGR 1. de las Rivas M, Daniel EJP, Narimatsu Y, Compañón I, Kato K ... Nat Chem Biol, 2020	76	2020
De novo expression of human polypeptide N-acetylgalactosaminyltransferase 6 (GalNAc-T6) in colon adenocarcinoma inhibits the differentiation of colonic epithelium K Lavrsen, S Dabelsteen, SY Vakhrushev, AMR Levann, AD Haue, ... Journal of Biological Chemistry 293 (4), 1298-1314, 2018	75	2018
Site-specific O-glycosylation of members of the low-density lipoprotein receptor superfamily enhances ligand interactions S Wang, Y Mao, Y Narimatsu, Z Ye, W Tian, CK Goth, E Lira-Navarrete, ... Journal of Biological Chemistry 293 (19), 7408-7422, 2018	74	2018
A glycogene mutation map for discovery of diseases of glycosylation L Hansen, A Lind-Thomsen, HJ Joshi, NB Pedersen, CT Have, Y Kong, ... Glycobiology 25 (2), 211-224, 2015	72	2015
Novel congenital disorder of O-linked glycosylation caused by GALNT2 loss of function M Zilmer, AC Edmondson, SA Khetarpal, V Alesi, MS Zaki, K Rostasy, ... Brain 143 (4), 1114-1126, 2020	70	2020

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