Author

Anne Nørremølle

Observed names: A Norremolle, A Nørremølle, A. Norremolle, A. Nørremølle, Anne Noerremoelle, Anne Norremolle, Nørremølle, Anne

Institution: University of Copenhagen

Observed institutions: University of Copenhagen, University of British Columbia, University of Kansas, Queen's University, Kingston General Hospital, Hospital for Sick Children, Copenhagen University Hospital, Rigshospitalet, University of California San Diego, National Hospital for Neurology and Neurosurgery, Child and Family Research Institute

ORCID: 0000-0003-2561-7683

Observed ORCID: 0000-0003-2561-7683

OpenAlex ID: A5061436028

CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion

2012 · J.-M. Lee, E.M. Ramos, et al. · Neurology · 382

Simulation based virtual learning environment in medical genetics counseling: an example of bridging the gap between theory and practice in medical education

2016 · Guido Makransky, Mads T. Bonde, et al. · BMC Medical Education · 168

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Inhibition of endoplasmic reticulum stress counteracts neuronal cell death and protein aggregation caused by N-terminal mutant huntingtin proteins

2008 · Sami Reijonen, Noora Putkonen, et al. · Experimental Cell Research · 154

A SNP in the HTT promoter alters NF-κB binding and is a bidirectional genetic modifier of Huntington disease

2015 · REGISTRY Investigators of the European Huntington's Disease Network, Kristina Bečanović, et al. · Nature Neuroscience · 134

Integrative Characterization of the R6/2 Mouse Model of Huntington’s Disease Reveals Dysfunctional Astrocyte Metabolism

2018 · Niels H. Skotte, Jens V. Andersen, et al. · Cell Reports · 94

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Fabry Disease Mimicking Hypertrophic Cardiomyopathy: Genetic Screening Needed for Establishing the Diagnosis in Women

2010 · Ole Havndrup, Michael Christiansen, et al. · European Journal of Heart Failure · 89

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Trinucleotide repeat elongation in the Huntingtin gene in Huntington Disease patients from 71 Danish families

1993 · Anne Nørremølle, Olaf Rless, et al. · Human Molecular Genetics · 87

Central 5-HT4 receptor binding as biomarker of serotonergic tonus in humans: a [11C]SB207145 PET study

2013 · M E Haahr, P M Fisher, et al. · Molecular Psychiatry · 86

Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation

2004 · J. E. Nielsen, B. Johnsen, et al. · European Journal of Neurology · 79

A clinical classification acknowledging neuropsychiatric and cognitive impairment in Huntington’s disease

2014 · Tua Vinther-Jensen, Ida U Larsen, et al. · Orphanet Journal of Rare Diseases · 68

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Reduction in mitochondrial DNA copy number in peripheral leukocytes after onset of Huntington's disease

2014 · Maria Hvidberg Petersen, Esben Budtz-Jørgensen, et al. · Mitochondrion · 62

Huntington’s Disease Does Not Appear to Increase the Risk of Diabetes Mellitus

2009 · T. W. Boesgaard, T. T. Nielsen, et al. · Journal of Neuroendocrinology · 49

Impaired Glucose Tolerance in the R6/1 Transgenic Mouse Model of Huntington’s Disease

2007 · K. Josefsen, M. D. Nielsen, et al. · Journal of Neuroendocrinology · 47

Dysfunctional mitochondrial respiration in the striatum of the Huntington’s disease transgenic R6/2 mouse model

2013 · Frederik Heurlin Aidt, Signe Marie Borch Nielsen, et al. · PLoS Currents · 45

Perturbations in the p53/miR-34a/SIRT1 pathway in the R6/2 Huntington's disease model

2017 · Regina Hertfelder Reynolds, Maria Hvidberg Petersen, et al. · Molecular and Cellular Neuroscience · 43

Reduced gluconeogenesis and lactate clearance in Huntington's disease

2010 · Knud Josefsen, Signe M.B. Nielsen, et al. · Neurobiology of Disease · 39

Inhibition of Huntingtin Synthesis by Antisense Oligodeoxynucleotides

2000 · Christine Nellemann, Kathrine Abell, et al. · Molecular and Cellular Neuroscience · 37

Correlation between magnitude of CAG repeat length alterations and length of the paternal repeat in paternally inherited Huntington's disease

1995 · Anne Nørremølle, Sven Asger Sørensen, et al. · Clinical Genetics · 36

Serotonin transporter gene (SLC6A4) variation and sensory processing sensitivity—Comparison with other anxiety‐related temperamental dimensions

2020 · Cecilie L. Licht, Erik L. Mortensen, et al. · Molecular Genetics & Genomic Medicine · 29

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A novel presenilin 2 mutation (V393M) in early‐onset dementia with profound language impairment

2008 · S. G. Lindquist, L. Hasholt, et al. · European Journal of Neurology · 25

DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington disease

2008 · Susan Andrew, Jane Theilmann, et al. · Clinical Genetics · 25

Antisense downregulation of mutant huntingtin in a cell model

2003 · Lis Hasholt, Kathrine Abell, et al. · The Journal of Gene Medicine · 25

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

2004 · Anne Nørremølle, Lis Hasholt, et al. · American Journal of Medical Genetics Part A · 24

Huntington's disease-like and ataxia syndromes: Identification of a family with a de novo SCA17/TBP mutation

2009 · Sara Bech, Thor Petersen, et al. · Parkinsonism & Related Disorders · 23

Dentatorubral‐pallidoluysian atrophy. Clinical features of a five‐generation danish family

1996 · J. E. Nielsen, S. A. Sørensen, et al. · Movement Disorders · 21

Works count: 67

Citation count: 2,129

H-index: 23

I10-index: 39