Inger Juncker - Concepedia

Author

Inger Juncker

Aarhus University Hospital

Also Known As

I Juncker, I. Juncker, INGER JUNCKER, Inger Juncker

Publications

312

Citations

H-Index

Concepts

All Affiliations

Aarhus University Hospital Lund University University of Copenhagen Statens Serum Institut Odense University Hospital

About

Inger Juncker is an author at Aarhus University Hospital specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	81
2	Pathology	4	4	81
3	Molecular Genetics	3	3	44
4	Biology	1	1	19
5	Neurology	1	1	37

Inger Juncker

Publications

306

Citations

H-Index

Page 1

	Year	Citations
Cardiac involvement in myotonic dystrophy: a nationwide cohort study Marie Lund, Lars Jorge Díaz, Mattis Flyvholm Ranthe, European Heart Journal	2014	65
X‐linked hypohidrotic ectodermal dysplasia. Genetic and dental findings in 67 Danish patients from 19 families MO Lexner, Allan Bardow, Inger Juncker, Clinical Genetics	2008	61
Detection of mutations in the<i>COL4A5</i>gene by SSCP in X-linked Alport syndrome Jens Michael Hertz, Inger Juncker, Ulf Persson, Human Mutation	2001	43
Low frequency of <i>Parkin</i>, <i>Tyrosine Hydroxylase</i>, and <i>GTP Cyclohydrolase I</i> gene mutations in a Danish population of early‐onset Parkinson's Disease Jens Michael Hertz, Karen Østergaard, Inger Juncker, European Journal of Neurology GeneticsPathologyDisease Gene IdentificationPark2 MutationDanish Population	2006	37
A novel missense mutation (402C → T) in exon 1 in the EDA gene in a family with X‐linked hypohidrotic ectodermal dysplasia Jens Michael Hertz, Karen Nørgaard Hansen, Inger Juncker, Clinical Genetics	1998	24
Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutation Dorte Haubek, Hans Gjørup, Lillian G. Jensen, International Journal of Paediatric Dentistry CytogeneticsGeneticsPathologyMolecular GeneticsGenomics	2011	19
Patients with Goodpasture's disease have two normal COL4A3 alleles encoding the NC1 domain of the type IV collagen 3 chain U Persson, Jens Michael Hertz, Martin Carlsson, Nephrology Dialysis Transplantation	2004	18
MLPA and cDNA analysis improves <i>COL4A5</i> mutation detection in X‐linked Alport syndrome Inger Juncker, Niels Marcussen Clinical Genetics GeneticsPathologyMolecular GeneticsDisease Gene IdentificationDermatology	2008	15
Risk of cancer in relatives of patients with myotonic dystrophy: a population‐based cohort study Marie Lund, Lars Jorge Díaz, S. Gørtz, European Journal of Neurology	2014	14
Alport syndrome caused by inversion of a 21 Mb fragment of the long arm of the X-chromosome comprising exon 9 through 51 of the COL4A5 gene Jens Michael Hertz, Ulf Persson, Inger Juncker, Human Genetics ChromatinMendelian DisorderCytogeneticsGenetic DisorderGenetics	2005	10

Page 1