Kathrin Giehl - Concepedia

Author

Kathrin Giehl

Ludwig-Maximilians-Universität München ORCID

Also Known As

Giehl, Kathrin, K Giehl, K. A. Giehl, K. Giehl, K.A. Giehl, Kathrin A Giehl, Kathrin A. Giehl, Kathrin Giehl, Kathrin A. Giehl

140

Publications

2.4K

Citations

H-Index

Concepts

All Affiliations

Ludwig-Maximilians-Universität München University of Cologne University of Bonn German Center for Neurodegenerative Diseases University Hospital Cologne

About

Kathrin Giehl is an author at Ludwig-Maximilians-Universität München specializing in medicine, genetics, and dermatology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	16	519
2	Biology	4	4	171
3	Health Sciences	3	3	66
4	Public Health	3	3	102
5	Social Sciences	1	1	31

Kathrin Giehl

Publications

1.7K

Citations

H-Index

Page 1

	Year	Citations
Neurocomputational mechanisms underlying subjective valuation of effort costs Trevor T.‐J. Chong, Matthew A J Apps, Kathrin Giehl, PLoS Biology	2017	429
Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia Zhimiao Lin, Quan Chen, Lei Shi, The American Journal of Human Genetics Somatic VariantGenetic DisorderGeneticsPathologyMolecular Genetics	2012	75
Nonsense Mutations in AAGAB Cause Punctate Palmoplantar Keratoderma Type Buschke-Fischer-Brauer Kathrin Giehl, Gertrud Eckstein, Sandra M. Pasternack, The American Journal of Human Genetics BiologyGeneticsMolecular GeneticsNonsense MutationsGenomics	2012	71
Dopamine metabolism of the nucleus accumbens and fronto-striatal connectivity modulate impulse control Jochen Hammes, Hendrik Theis, Kathrin Giehl, Brain	2019	68
Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss Silke Redler, F.F. Brockschmidt, Rachid Tazi‐Ahnini, British Journal of Dermatology	2012	61
Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata Lina M Forstbauer, Felix F Brockschmidt, Valentina Moskvina, European Journal of Human Genetics BiologyGenome-wide Association StudyAllelic VariantGenome StudyGenetics	2011	54
Association of pyrin mutations and autoinflammation with complex phenotype hidradenitis suppurativa: a case–control study Seçil Vural, Mustafa Gündoğdu, Ezgi Gökpınar İli, British Journal of Dermatology Systemic DiseasesImmunodeficienciesGenetic EpidemiologyPathologyDermatology	2018	53
Protein expression of melanocyte growth factors (bFGF, SCF) and their receptors (FGFR‐1, c‐kit) in nevi and melanoma Kathrin Giehl, Ursula Nägele, Matthias Volkenandt, Journal of Cutaneous Pathology	2006	51
Characterization and expression analysis of the hair keratin associated protein KAP26.1 Michael A. Rogers, Lutz Langbein, Silke Praetzel‐Wunder, British Journal of Dermatology	2008	50
Neural Correlates of Hypokinetic Dysarthria and Mechanisms of Effective Voice Treatment in Parkinson Disease Alexander Baumann, Adelheid Nebel, Oliver Granert, Neurorehabilitation and neural repair	2018	45

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