Andreas Hahn - Concepedia

Author

Andreas Hahn

Also Known As

A F Hahn, A Hahn, A. Hahn, Alba A. Hahn, Alexander Hahn, Alisa Hahn, Andreas Hahn, Hahn, AF, Hahn, Alexander, Hahn, Andreas

201

Publications

3.8K

Citations

H-Index

104

Concepts

All Affiliations

Justus-Liebig-Universität Gießen Heidelberg University University Hospital Heidelberg University Hospital Münster Charité - Universitätsmedizin Berlin

About

Andreas Hahn is an author at Justus-Liebig-Universität Gießen specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	28	1.3K
2	Health Sciences	3	3	191
3	Public Health	2	2	42
4	Social Sciences	1	1	18
5	Allergy	1	1	31

Andreas Hahn

Publications

3.2K

Citations

H-Index

Page 1

	Year	Citations
Mutations in a Gene Encoding a Novel SH3/TPR Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy Jan Senderek, Carsten Bergmann, Claudia Stendel, The American Journal of Human Genetics Neurodegenerative DiseasesMolecular NeuroscienceMendelian DisorderGenetic DisorderGenetics	2003	210
Clinical implications of maximal respiratory pressure determinations for individuals with duchenne muscular dystrophy Andreas Hahn, John R. Bach, Anne Delaubier, Archives of Physical Medicine and Rehabilitation Clinical ImplicationsKinesiologyClinical PhysiologyDuchenne Muscular DystrophyExercise Physiology	1997	151
Evaluation of Children with SMA Type 1 Under Treatment with Nusinersen within the Expanded Access Program in Germany Astrid Pechmann, Thorsten Langer, David Schorling, Journal of Neuromuscular Diseases	2018	144
Recessive TRAPPC11 Mutations Cause a Disease Spectrum of Limb Girdle Muscular Dystrophy and Myopathy with Movement Disorder and Intellectual Disability Nina Bögershausen, Nassim Shahrzad, Jessica X. Chong, The American Journal of Human Genetics Genetic DisorderMedicineGeneticsPathologyDisease Spectrum	2013	118
47 patients with FLNA associated periventricular nodular heterotopia Max Lange, Burkhard S. Kasper, Axel Bohring, Orphanet Journal of Rare Diseases	2015	105
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation Karim Kouz, Stephanie Spranger, Diana Mitter, Genetics in Medicine Mendelian DisorderAutoimmune DiseaseGenetic DisorderGeneticsGenetic Epidemiology	2016	104
<i>KCNQ2</i> and <i>KCNQ3</i> mutations contribute to different idiopathic epilepsy syndromes Bernd A. Neubauer, Siegfried Waldegger, Jolanta Heinzinger, Neurology	2008	96
Atypical “Benign” Partial Epilepsy or Pseudo-Lennox Syndrome. Part I: Symptomatology and Long-Term Prognosis Andreas Hahn, J. Pistohl, Bernd A. Neubauer, Neuropediatrics	2001	91
Mutations of <i>KIF14</i> cause primary microcephaly by impairing cytokinesis Abubakar Moawia, Ranad Shaheen, Sajida Rasool, Annals of Neurology	2017	83
Dihydropyrimidinase deficiency: Phenotype, genotype and structural consequences in 17 patients André B. P. Kuilenburg, Doreen Dobritzsch, Judith Meijer, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseThyroid Hormone	2010	81

Page 1