F.F. Brockschmidt - Concepedia

Author

F.F. Brockschmidt

Life & Brain (Germany)

Also Known As

F Brockschmidt, F F Brockschmidt, F. F Brockschmidt, F.F. Brockschmidt

Publications

561

Citations

H-Index

Concepts

All Affiliations

Life & Brain (Germany)University of Bonn Institut für Medizinische Biometrie, Informatik und Epidemiologie Ludwig-Maximilians-Universität München Heinrich Heine University Düsseldorf

About

F.F. Brockschmidt is an author at Life & Brain (Germany) specializing in genetics, medicine, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	215
2	Social Sciences	1	1	103
3	Endocrinology	1	1	37
4	Molecular Genetics	1	1	37
5	Neurology	1	1	103

F.F. Brockschmidt

Publications

450

Citations

H-Index

Page 1

	Year	Citations
First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children Darina Roeske, Kerstin U. Ludwig, Nina Neuhoff, Molecular Psychiatry Molecular NeuroscienceNeurophysiological Endophenotypes PointsDyslexic ChildrenGeneticsTrans-regulation Effects	2009	103
Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples Stéphanie Le Hellard, Thomas W. Mühleisen, Srdjan Djurovic, Molecular Psychiatry PsychiatryPsychotic DisorderGeneticsPsychiatric GeneticsGenetic Epidemiology	2008	75
Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness F.F. Brockschmidt, Justine A. Ellis, Sibylle Eigelshoven, British Journal of Dermatology	2011	69
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
Evidence for a polygenic contribution to androgenetic alopecia F.F. Brockschmidt, Axel M. Hillmer, S. Hanneken, British Journal of Dermatology	2013	46
Investigation of selected cytokine genes suggests that <i>IL2RA</i> and the <i>TNF</i> / <i>LTA</i> locus are risk factors for severe alopecia areata Silke Redler, Florian Albert, F.F. Brockschmidt, British Journal of Dermatology	2012	39
The two most common alleles of the coding GGN repeat in the androgen receptor gene cause differences in protein function F.F. Brockschmidt, Markus M. Nöthen, Axel M. Hillmer Journal of Molecular Endocrinology Androgen ReceptorPolyglycine TractGeneticsHuman PolymorphismGenomic Mechanism	2007	37
The <i>TRAF1/C5</i> locus confers risk for familial and severe alopecia areata Silke Redler, F.F. Brockschmidt, Lina M Forstbauer, British Journal of Dermatology	2009	20

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