Birgit Köhler - Concepedia

Author

Birgit Köhler

Also Known As

B Kohler, B Köhler, B. Kohler, B. Köhler, Birgit Kohler, Birgit Köhler, Birgit Köhler, Birgit M. Köhler, Birgit Maria Köhler, Köhler, Birgit

Publications

1.2K

Citations

H-Index

Concepts

All Affiliations

Humboldt-Universität zu Berlin Charité - Universitätsmedizin Berlin Heidelberg University Technical University of Munich Freie Universität Berlin

About

Birgit Köhler is an author at Humboldt-Universität zu Berlin specializing in medicine, pathology, and iodine deficiency disorders.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	213
2	Public Health	2	2	86
3	Education	1	1	22
4	Health Sciences	1	1	31
5	Allergy	1	1	12

Birgit Köhler

Publications

711

Citations

H-Index

Page 1

	Year	Citations
Five novel mutations in steroidogenic factor 1 (SF1,NR5A1) in 46,XY patients with severe underandrogenization but without adrenal insufficiency Birgit Köhler, Lin Lin, Bruno Ferraz‐de‐Souza, Human Mutation	2007	155
Severe Hepatotoxicity During Valproate Therapy: An Update and Report of Eight New Fatalities Armin König, H. Siemes, F Bläker, Epilepsia	1994	134
Mutations of Genes Involved in the Innate Immune System as Predictors of Sepsis in Very Low Birth Weight Infants Peter Ahrens, E Kattner, Birgit Köhler, Pediatric Research InflammationPathogenesisImmunologyInnate Immune SystemSepsis	2004	128
Transient congenital hypothyroidism and hyperthyrotropinemia: normal thyroid function and physical development at the ages of 6-14 years. Birgit Köhler, Dirk Schnabel, Heike Biebermann, The Journal of Clinical Endocrinology & Metabolism Normal Thyroid FunctionThyroid FunctionIodine Deficiency DisordersThyroid Disease6-14 Years	1996	64
IL1-blocking therapy in colchicine-resistant familial Mediterranean fever Birgit Köhler, Hanns‐Martin Lorenz, Norbert Blank European Journal of Rheumatology	2018	35
Coexpression of Wilms’ tumor suppressor 1 (WT1) and androgen receptor (AR) in the genital tract of human male embryos and regulation of AR promoter activity by WT1 Birgit Köhler, Anne-Lise Delezoide, Brigitte Boizet-Bonhoure, Journal of Molecular Endocrinology	2007	33
A method to assess 59Fe in residual tissue blood content in mice and its use to correct 59Fe-distribution kinetics accordingly Klaus Schümann, Bernadett Szegner, Birgit Köhler, Toxicology Animal PhysiologyMedicineIn Vivo SystemBioanalysisPhysiology	2007	31
An N-terminal WT1 mutation (P181S) in an XY patient with ambiguous genitalia, normal testosterone production, absence of kidney disease and associated heart defect: enlarging the phenotypic spectrum of WT1 defects Birgit Köhler, Catherine Pienkowski, F Audran, European Journal of Endocrinology	2004	31
A Novel Hemizygous Mutation of <b><i>MAMLD1</i></b> in a Patient with 46,XY Complete Gonadal Dysgenesis Inge-Lore Ruiz-Arana, Angela Hübner, Cigdem Cetingdag, Sexual Development	2015	24
Screening for mutations of the human thyroid peroxidase gene in patients with congenital hypothyroidism Annette Grüters, Birgit Köhler, Annika Wolf, Experimental and Clinical Endocrinology & Diabetes Ggcc DuplicationThyroid Hormone BiosynthesisGeneticsIodine Deficiency DisordersThyroid Disease	2009	24

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