M. Lodahl

发表

Regulation of the CD56 promoter and its association with proliferation, anti-apoptosis and clinical factors in multiple myeloma

L. Knudsen, P. Gimsing, T. Rasmussen, 2009, Leukemia and Lymphoma.

Possible roles for activating RAS mutations in the MGUS to MM transition and in the intramedullary to extramedullary transition in some plasma cell tumors.

H. Johnsen, M. Kuehl, T. Rasmussen, 2005, Blood.

Occurrence of dysregulated oncogenes in primary plasma cells representing consecutive stages of myeloma pathogenesis: indications for different disease entities

H. Johnsen, K. Theilgaard-Mönch, T. Rasmussen, 2003, British journal of haematology.

Dysregulation of CD47 and the ligands thrombospondin 1 and 2 in multiple myeloma

L. Knudsen, T. Rasmussen, I. Dahl, 2007, British journal of haematology.

Identification of translocation products but not K-RAS mutations in memory B cells from patients with multiple myeloma

H. Johnsen, M. Kuehl, L. Knudsen, 2010, Haematologica.

Optic nerve histopathology in a case of Wolfram Syndrome: a mitochondrial pattern of axonal loss.

N. Miller, T. Albini, V. Carelli, 2013, Mitochondrion.

plasma cell tumors transition and in the intramedullary to extramedullary transition in some Possible roles for activating RAS mutations in the MGUS to MM

M. Kuehl, T. Rasmussen, M. Lodahl, 2013 .

Expression of HOXA Genes in Patients with Multiple Myeloma

H. Johnsen, T. Rasmussen, H. Hudlebusch, 2004, Leukemia & lymphoma.

Identification and analysis of deletion breakpoints in four Mohr-Tranebjærg syndrome (MTS) patients

J. Tolmie, N. Tommerup, H. Karstensen, 2022, Scientific Reports.

Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment

K. Arnos, A. Pandya, M. Bitner-Glindzicz, 2011, American journal of medical genetics. Part A.

Rapidly progressive renal disease as part of Wolfram syndrome in a large inbred Turkish family due to a novel WFS1 mutation (p.Leu511Pro).

M. Dogan, L. Tranebjærg, H. Boulahbel, 2012, European journal of medical genetics.

A novel mutation in the connexin 26 gene (GJB2) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome

U. Koppelhus, L. Tranebjærg, M. Sommerlund, 2011, Clinical and experimental dermatology.

Mutation update on the CHD7 gene involved in CHARGE syndrome

M. Swertz, L. Hoefsloot, R. Hofstra, 2012, Human mutation.

Upregulated MCL1 mRNA expression in multiple myeloma lacks association with survival

L. Knudsen, T. Rasmussen, I. Dahl, 2009, British journal of haematology.

The Global State of the Genetic Counseling Profession

A. Obregon-Tito, K. Ormond, R. Moldovan, 2018, European Journal of Human Genetics.

Two new cases with microdeletion of 17q23.2 suggest presence of a candidate gene for sensorineural hearing loss within this region

Z. Tümer, K. Brøndum‐Nielsen, A. Ronan, 2011, American journal of medical genetics. Part A.

Myeloma cell expression of 10 candidate genes for osteolytic bone disease. Only overexpression of DKK1 correlates with clinical bone involvement at diagnosis

M. Thomassen, N. Abildgaard, L. Knudsen, 2007, British journal of haematology.

Identification of ID‐1 as a potential target gene of MMSET in multiple myeloma

H. Johnsen, K. Theilgaard-Mönch, T. Rasmussen, 2005, British journal of haematology.

GJB2 (Connexin-26) mutations are not frequent among hearing impaired patients in East Greenland

H. Eiberg, P. Homøe, L. Tranebjærg, 2012, International journal of audiology.

Phenotypic variability in a seven-generation Swedish family segregating autosomal dominant hearing impairment due to a novel EYA4 frameshift mutation.

N. Dahl, J. Klar, L. Tranebjærg, 2015, Gene.

Phenotypic subregions within the split-hand/foot malformation 1 locus

Malene B. Rasmussen, S. Kreiborg, E. Budtz-Jørgensen, 2016, Human Genetics.

The phenotypic spectrum of dystonia in Mohr–Tranebjaerg syndrome

V. Fung, C. Sue, D. Rowe, 2012, Movement disorders : official journal of the Movement Disorder Society.

SLC26A4 mutation frequency and spectrum in 109 Danish Pendred syndrome/DFNB4 probands and a report of nine novel mutations

Z. Tümer, R. Wetke, T. Fagerheim, 2013, Clinical genetics.

Homoplasmy of the G7444A mtDNA and heterozygosity of the GJB2 c.35delG mutations in a family with hearing loss.

G. Korres, Y. Gyftodimou, M. Petersen, 2011, International journal of pediatric otorhinolaryngology.

In Multiple Myeloma Clonotypic CD38 − /CD19 + /CD27 + Memory B Cells Recirculate Through Bone Marrow, Peripheral Blood and Lymph Nodes

H. Johnsen, S. Hancke, T. Rasmussen, 2004, Leukemia & lymphoma.

Characterization of potential CD138 negative myeloma “stem cells”

N. Abildgaard, T. Rasmussen, J. H. Christensen, 2012, Haematologica.

Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment

K. Arnos, A. Pandya, M. Bitner-Glindzicz, 2011, American journal of medical genetics. Part A.

Optic nerve histopathology in a case of Wolfram Syndrome: a mitochondrial pattern of axonal loss.

T. Albini, V. Carelli, A. Sadun, 2013, Mitochondrion.