Prokisch H
机构: Institute of Human Genetics TU-Munich
每年引用次数
引用次数
引用: 53,545
H-指数: 102
I10-指数 : 311
出版物: 587
Targeted gene expression analysis in Parkinson's disease and ageing
H Prokisch , M Elstner , D Turnbull , C Morris
Journal of Neurology
2007
High symmetry of visual field loss in X-linked retinitis pigmentosa
H Prokisch , R E MacLaren , S Ramsden , N Gloeckle
Investigative Ophthalmology & Visual Science 57 ( 12) 132 -132
2016
Integrative analysis of the mitochondrial proteome
H Prokisch , T Meitinger , C Andreoli , C Scharfe
19 -19
1
2004
mitoNET-German network for mitochondrial disorders: progress report after 2 years duration
M Deschauer , M Schulke-Gerstenfeld , I Wittig , T Meitinger
197 -197
2011
MULTIPLE MITOCHONDRIAL DYSFUNCTION SYNDROME CAUSED BY A MUTATION IN BOLA3
B Haberberger , I Wittig , T Meitinger , TB Haack
2012
FIBRE TYPE-SPECIFIC WHOLE-GENOME EXPRESSION PROFILING OF HUMAN SKELETAL MUSCLES
H Katharina , S Brosel , C Kammerlander , T Klopstock
Orthopaedic Proceedings
2018
Exome sequencing in 30 neurodegeneration with brain iron accumulation patients
T Haack , M Hartig , T Wieland , T Schwarzmayr
Neuropediatrics 44 ( 02)
2013
Mitochondriopathy due to mutations in MTFMT: a predominant neurologic phenotype
P Freisinger , T Haack , R Kopajtich , M Johannes
Neuropediatrics 44 ( 02)
1
2013
The German network for mitochondrial disorders (mitoNET)
B Büchner , H Prokisch , T Meitinger , U Ahting
Neuropediatrics 44 ( 02)
2013
Molecular diagnosis in mitochondrial respiratory chain deficiency using exome sequencing
R Kopajtich , T Haack , B Haberberger , J Mayr
Neuropediatrics 44 ( 02)
2013
Treat Iron-Related Childhood-Onset Neurodegeneration (TIRCON) - an integrated strategy under FP7 to improve research, treatment, and care in neurodegeneration with brain iron accumulation
M Hartig , O Sibon , S Hayflick , T Kmiec
Neuropediatrics 44 ( 02)
1
2013
Band-like calcification with simplified gyration and polymicrogyria: further delineation of phenotype and review of literature
C Siegel , TB Haack , C Makowski , U Tauer
Neuropediatrics 44 ( 02)
2013
Clinical symptoms of six children with thiamin pyrophosphokinase deficiency
J Koch , JA Mayr , T Scheffner , C Makowski
Neuropediatrics 44 ( 02)
2013
Mitochondrial Encephalopathies caused by defective mitochondrial translation
E Wilichowski , H Prokisch , T Meitinger , J Gärtner
Neuropediatrics 43 ( 02)
2012
Effects of an isocaloric high-protein diet on inflammatory status in type 2 diabetes
O Pivovarova , M Markova , S Hornemann , S Sucher
Diabetologie Und Stoffwechsel 10 103
2015
A high-protein diet reduces liver fat content and improves glomerular filtration rate in subjects with type 2 diabetes
M Markova , S Hornemann , S Sucher , C Herder
Diabetologie Und Stoffwechsel 10 157
2015
Genexpressionsanalyse dopaminerger Zellen der Substantia nigra im Parkinson-Syndrom
M Elstner , C Morris , D Metha , M Mader
Aktuelle Neurologie 34 636
2007
A DNA methylation biomarker of alcohol consumption.
C Liu , R E Marioni , Å K Hedman , L Pfeiffer
Molecular Psychiatry 23 ( 2) 422 -433
285
2018
Defective NDUFA9 as a novel cause of neonatally fatal complex I disease
B J C van den Bosch , M Gerards , W Sluiter , A P A Stegmann
Journal of Medical Genetics 49 ( 1) 10 -15
32
2012
Assoziation zwischen der genomweiten Genexpression im humanen Vollblut und Nüchtern- sowie 2-Stunden-Glukose: KORA F4 Studie
M Carstensen , C Herder , S Landwehr , W Rathmann
Diabetologie Und Stoffwechsel 6 ( 04)
2011