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Clemens R. Müller

Observed names: C MULLER, Clemens Müller, Clemens R Müller, Clemens R Müller, Clemens R. Muller, Clemens R. Müller, Clemens Rainer Müller, Clemens R. Müller, Müller, Clemens
Observed institutions: National Institutes of Health, University of Bonn, Max Planck Society, University of Freiburg, University of Cologne, Max Delbrück Center, University of Würzburg, University Hospital Bonn, University Medical Center Freiburg, McMaster Children's Hospital, German Red Cross, Amsterdam Neuroscience, National Institute of Neurological Disorders and Stroke, Universitätsklinikum Würzburg, Max Planck Institute for Molecular Genetics, St. Franziskus Hospital, Donders Institute for Brain, Cognition and Behaviour, Amsterdam UMC Location Vrije Universiteit Amsterdam
OpenAlex ID: A5107599722
Association of Anxiety-Related Traits with a Polymorphism in the Serotonin Transporter Gene Regulatory Region
1996 · Klaus-Peter Lesch, Dietmar Bengel, et al. · Science · 5,166
Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2
2004 · Simone Rost, Andreas Fregin, et al. · Nature · 1,134
Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy
1999 · Kristen J. Nowak, Duangrurdee Wattanasirichaigoon, et al. · Nature Genetics · 408
The Genetic Basis of Resistance to Anticoagulants in Rodents
2005 · Hans-Joachim Pelz, Simone Rost, et al. · Genetics · 348
VKORC1 haplotypes and their impact on the inter-individual and inter-ethnical variability of oral anticoagulation
2005 · Christof Geisen, Matthias Watzka, et al. · Thrombosis and Haemostasis · 259
Novel mutations in the VKORC1 gene of wild rats and mice – a response to 50 years of selection pressure by warfarin?
2009 · Simone Rost, Hans-Joachim Pelz, et al. · BMC Genetics · 158
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Magnetic resonance imaging of muscle in congenital myopathies associated with RYR1 mutations
2004 · Heinz Jungbluth, Mark R. Davis, et al. · Neuromuscular Disorders · 158
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification
2019 · Michael T. Parsons, Emma Tudini, et al. · Human Mutation · 145
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Identification of Novel Mutations in the Ryanodine-Receptor Gene (RYR1) in Malignant Hyperthermia: Genotype-Phenotype Correlation
1998 · Bernadette M. Manning, Kathleen A. Quane, et al. · The American Journal of Human Genetics · 135
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BRIP1 loss-of-function mutations confer high risk for familial ovarian cancer, but not familial breast cancer
2018 · Nana Weber-Lassalle, Jan Hauke, et al. · Breast Cancer Research · 133
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Targeted Molecular Analysis in Adrenocortical Carcinomas: A Strategy Toward Improved Personalized Prognostication
2018 · Juliane Lippert, Silke Appenzeller, et al. · The Journal of Clinical Endocrinology & Metabolism · 118
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Diagnostic approach for FSHD revisited: SMCHD1 mutations cause FSHD2 and act as modifiers of disease severity in FSHD1
2014 · Mirjam Larsen, Simone Rost, et al. · European Journal of Human Genetics · 114
Human Vitamin K 2,3-Epoxide Reductase Complex Subunit 1-like 1 (VKORC1L1) Mediates Vitamin K-dependent Intracellular Antioxidant Function
2011 · Philipp Westhofen, Matthias Watzka, et al. · Journal of Biological Chemistry · 113
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Vitamin K Epoxide Reductase Complex Subunit 1 (VKORC1): The Key Protein of the Vitamin K Cycle
2006 · Johannes Oldenburg, Carville G. Bevans, et al. · Antioxidants and Redox Signaling · 112
Effect of Ryanodine Receptor Mutations on Interleukin-6 Release and Intracellular Calcium Homeostasis in Human Myotubes from Malignant Hyperthermia-susceptible Individuals and Patients Affected by Central Core Disease
2004 · Sylvie Ducreux, Francesco Zorzato, et al. · Journal of Biological Chemistry · 108
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Site-directed mutagenesis of coumarin-type anticoagulant-sensitive VKORC1
2005 · Simone Rost, Andreas Fregin, et al. · Thrombosis and Haemostasis · 101
Missense mutations at ALA‐10 in the factor IX propeptide: an insignificant variant in normal life but a decisive cause of bleeding during oral anticoagulant therapy
1997 · Johannes Oldenburg, Ernst‐Markus Quenzel, et al. · British Journal of Haematology · 97
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Association Between Loss-of-Function Mutations Within the FANCM Gene and Early-Onset Familial Breast Cancer
2016 · Guido Neidhardt, Jan Hauke, et al. · JAMA Oncology · 84
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Evaluation of DHPLC in the analysis of hemophilia A
2001 · Johannes Oldenburg, Vytautas Ivaskevicius, et al. · Journal of Biochemical and Biophysical Methods · 83
Detection of a novel RYR1 mutation in four malignant hyperthermia pedigrees
1994 · Katherine E. Keating, Kathleen A. Quane, et al. · Human Molecular Genetics · 78
Compound heterozygous mutations in the γ‐glutamyl carboxylase gene cause combined deficiency of all vitamin K‐dependent blood coagulation factors
2004 · Simone Rost, Andreas Fregin, et al. · British Journal of Haematology · 76
Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6
2013 · Simone Rost, Elisa Bach, et al. · European Journal of Human Genetics · 74
Homozygosity mapping of a second gene locus for hereditary combined deficiency of vitamin K–dependent clotting factors to the centromeric region of chromosome 16
2002 · Andreas Fregin, Simone Rost, et al. · Blood · 74
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Nesprin-2 giant safeguards nuclear envelope architecture in LMNA S143F progeria cells
2007 · Sebastian Kandert, Yvonne Lüke, et al. · Human Molecular Genetics · 72
VKORC1 deficiency in mice causes early postnatal lethality due to severe bleeding
2009 · Gabriele Spohn, Andre Kleinridders, et al. · Thrombosis and Haemostasis · 68
Works count: 87
Citation count: 10,690
H-index: 37
I10-index: 63
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