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Hassnaa Mahmoudi
Hassnaa Mahmoudi
University of Bonn
Biology
Hypotrichosis
Hair loss
Genotype
Diabetes mellitus
4
Papers
30
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Identification of a novel mutation in RIPK4 in a kindred with phenotypic features of Bartsocas-Papas and CHAND syndromes
2015
American Journal of Medical Genetics Part A
Benjamin Gollasch
Fitnat Buket Basmanav
Arti Nanda
Günter Fritz
Hassnaa Mahmoudi
Holger Thiele
Maria Wehner
Sabrina Wolf
Janine Altmüller
Peter Nürnberg
Jorge Frank
Regina C. Betz
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Citations (8)
Alopecia and Hypotrichosis as Characteristic Findings in Woodhouse-Sakati Syndrome: Report of a Family with Mutation in the C2orf37 Gene
2014
Pediatric Dermatology
D.N.B.E. Arti Nanda M.D.
Sandra M. Pasternack
Hassnaa Mahmoudi
B S Nina Ishorst
Ramon Grimalt
Regina C. Betz
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Citations (10)
Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss
2013
Archives of Dermatological Research
Hassnaa Mahmoudi
Silke Redler
Pattie Birch
Dmitriy Drichel
K. Dobson
Rachid Tazi-Ahnini
Peter Teßmann
Kathrin A. Giehl
Roland Kruse
Gerhard Lutz
S. Hanneken
Hans Wolff
Ulrike Blume-Peytavi
Tim Becker
Markus M. Nöthen
Andrew G. Messenger
Markus Böhm
Regina C. Betz
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Citations (9)
Identification of an Alu-mediated 12.2-kb deletion of the complete LPAR6 (P2RY5) gene in a Turkish family with hypotrichosis and woolly hair
2012
Experimental Dermatology
Hassnaa Mahmoudi
Esra Tug
Ali Haydar Parlak
Halil Ibrahim Atasoy
Michael Ludwig
Mualla Polat
Sandra M. Pasternack
Regina C. Betz
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Citations (3)
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