Lisbeth Birk Møller

Author

Lisbeth Birk Møller

Also Known As

L B Møller, L Birk Moller, L MOLLER, L Møller, L. B. Moller, L. B. Møller, L. Birk Moller, L. Birk Møller, L. Birk‐Møller, L.B Møller

145

Publications

4.6K

Citations

H-Index

Concepts

All Affiliations

Kennedy Center University of Copenhagen Copenhagen University Hospital Rigshospitalet Aarhus University Hospital

About

Lisbeth Birk Møller is an author at Kennedy Center specializing in medicine, genetics, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	24	1.2K
2	Natural Sciences	10	10	609
3	Biochemistry	10	10	995
4	Social Sciences	3	3	185
5	Cellular Physiology	1	1	63

Lisbeth Birk Møller

Publications

3.3K

Citations

H-Index

Page 1

	Year	Citations
Crystal structure of a copper-transporting PIB-type ATPase Pontus Gourdon, Xiangyu Liu, Tina Skjørringe, Nature Crystal StructureBiochemistryMetalloproteinProtein X-ray CrystallographyStructure-function Enzyme Kinetics	2011	334
Missense dopamine transporter mutations associate with adult parkinsonism and ADHD Tina Skjørringe, Saiqa Yasmeen, Natascha V. Arends, Journal of Clinical Investigation NeurotransmitterMolecular BiologySynaptic SignalingSocial SciencesNeurology	2014	149
Mannose 6-Phosphate/Insulin-like Growth Factor–II Receptor Targets the Urokinase Receptor to Lysosomes via a Novel Binding Interaction Anders Nykjær, Erik I. Christensen, Henrik Vorum, The Journal of Cell Biology	1998	138
Similar Splice-Site Mutations of the ATP7A Gene Lead to Different Phenotypes: Classical Menkes Disease or Occipital Horn Syndrome Lisbeth Birk Møller, Zeynep Tümer, Connie Lund, The American Journal of Human Genetics Classical Menkes DiseaseMendelian DisorderGenetic DisorderGeneticsPathogenesis	2000	127
Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy Cathrine Jespersgaard, Mingyan Fang, Mette Bertelsen, Scientific Reports	2019	120
Copper-transporting P-type ATPases use a unique ion-release pathway Magnus Andersson, Daniel Mattle, Oleg Sitsel, Nature Structural & Molecular Biology BiochemistryBioenergeticsMembrane TransportNatural SciencesMetalloprotein	2013	114
Control of copper homeostasis in Escherichia coli by a P-type ATPase, CopA, and a MerR-like transcriptional activator, CopR Carsten Tilbæk Petersen, Lisbeth Birk Møller Gene P-type AtpaseBiochemistryNatural SciencesMetalloproteinBacteriology	2000	111
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients Crystel Bonnet, Zied Riahi, Sandra Chantot‐Bastaraud, European Journal of Human Genetics	2016	106
Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin Peter Huppke, Cornelia Brendel, Vera M. Kalscheuer, The American Journal of Human Genetics Mendelian DisorderOphthalmologyGenetic DisorderMedicineGenetics	2012	101
Impairment of Interrelated Iron- and Copper Homeostatic Mechanisms in Brain Contributes to the Pathogenesis of Neurodegenerative Disorders Tina Skjørringe, Lisbeth Birk Møller, Torben Moos Frontiers in Pharmacology	2012	96

Page 1