felix f brockschmidt - Inst Human Genet, Univ Bonn

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论文共 47 篇作者统计合作学者相似作者

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Abelson Helper Integration Site 1 Haplotypes and Peripheral Blood Expression Associates with Lithium Response and Immunomodulation in Bipolar Patients

Kosma Sakrajda,Karolina Bilska,Piotr M. Czerski,Beata Narożna,Monika Dmitrzak-Węglarz,Stefanie Heilmann-Heimbach,Felix F. Brockschmidt,Stefan Herms,Markus M. Nöthen,Sven Cichon,Barbara Więckowska,Janusz K. Rybakowski,Joanna Pawlak,Aleksandra Szczepankiewicz

Psychopharmacology（2023）

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血管新生およびリンパ管形成経路における単一ヌクレオチド多型はWuchereria bancroftiによって引き起こされるリンパ浮腫と関連する【JST・京大機械翻訳】

Debrah Linda Batsa,Albers Anna,Debrah Alexander Yaw,F Brockschmidt Felix,Tim Becker,Herold Christine,Hofmann Andrea,Osei-Mensah Jubin,Yusif Mubarik,Frohlich Holger, A. Hoerauf,Pfarr Kenneth

openalex（2017）

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Single Nucleotide Polymorphisms in the Angiogenic and Lymphangiogenic Pathways Are Associated with Lymphedema Caused by Wuchereria Bancrofti

Linda Batsa Debrah,Anna Albers,Alexander Yaw Debrah,Felix F. Brockschmidt,Tim Becker,Christine Herold,Andrea Hofmann,Jubin Osei-Mensah,Yusif Mubarik,Holger Fröhlich,Achim Hoerauf,Kenneth Pfarr

Human Genomics（2017）

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SINGLE NUCLEOTIDE POLYMORPHISMS IN ANGIOGENIC AND INFLAMMATION PATHWAY GENES ARE ASSOCIATED WITH PATENT LYMPHATIC FILARIASIS

Jubin Osei-Mensah,Linda Batsa-Debrah,Anna Albers, Lydia Lust,Felix Brockschmidt,Christine Herold,Yusif Mubarik,Tim Becker,Holger Froehlich Froehlich,Kenneth Pfarr,Achim Hoerauf,Alex Debrah

AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE（2015）

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Microdeletions Including Fmr1 in Three Female Patients with Intellectual Disability - Further Delineation of the Phenotype and Expression Studies

A. M. Zink,E. Wohlleber,H. Engels,O. K. Rodningen,K. Ravn,S. Heilmann,J. Rehnitz,N. Katzorke,C. Kraus, S. Blichfeldt,P. Hoffmann,H. Reutter,F. F. Brockschmidt,M. Kreiss-Nachtsheim,P. H. Vogt, T. E. Prescott,Z. Tumer,J. A. Lee

MOLECULAR SYNDROMOLOGY（2014）

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RE(ACT)2014 Rare Diseases. 2nd International Congress on Research of Rare and Orphan Diseases. 5th to 8th March 2014, Gehry Building, Novartis Campus, Basel: Abstracts

Molecular Syndromology（2014）

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Genome-Wide Association Study and Mouse Expression Data Identify A Highly Conserved 32 Kb Intergenic Region Between Wnt3 and Wnt9b As Possible Susceptibility Locus for Isolated Classic Exstrophy of the Bladder

HUMAN MOLECULAR GENETICS（2014）

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RE(ACT)2014Rare Diseases. 2nd International Congress on Research of Rare and Orphan Diseases. 5th to 8th March 2014, Gehry Building, Novartis Campus, Basel: Abstracts

Benjamin D. Solomon,F. Hadžiselimović,N.O. Hadziselimovic,P. Demougin,Edward J. Oakeley,Hartmut Engels,Alexander M. Zink,Eva Wohlleber,Olaug K. Rødningen,Kirstine Ravn,Stefanie Heilmann‐Heimbach, Julia Rehnitz,N. Katzorke,Cornelia Kraus, Susanne Blichfeldt, Peter M. Hoffmann,Heiko Reutter,F.F. Brockschmidt,Martina Kreiß‐Nachtsheim,P. H. Vogt,Trine Prescott,Zeynep Tümer, Jaimy Lee,Zehra Oya Uyguner, Mehmet Kocaoğlu,Güven Toksoy, Seniha Başaran, Hülya Kayserili,C. Dubourg, Frédérique Bonnet‐Brilhault,A. Toutain,C. Mignot,A. Jacquette,A. Dieux,M. Gérard,M.-P. Beaumont-Epinette,Sophie Julia,Bertrand Isidor, Matteo Rossi,Sylvie Odent,Claude Bendavid,C Barthélémy,Alain Verloès, Valentin David,Oussama M’Hamdi,Inès Ouertani,Habiba Chaabouni-Bouhamed,Satz Mengensatzproduktion,Druckerei Stückle

Molecular Syndromologyno. 2 (2014): 87-99

引用2浏览0引用

Evidence for A Polygenic Contribution to Androgenetic Alopecia

S. Heilmann,F. F. Brockschmidt,A. M. Hillmer,S. Hanneken,S. Eigelshoven,K. U. Ludwig,C. Herold,E. Mangold,T. Becker,R. Kruse,M. Knapp,M. M. Noethen

BRITISH JOURNAL OF DERMATOLOGYno. 4 (2013): 927-930

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