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Birgit Köhler

Observed names: B Kohler, B Köhler, B. Kohler, B. Köhler, Birgit Köhler, Köhler, Birgit
Observed institutions: Inserm, Philipps University of Marburg, Justus-Liebig-Universität Gießen, Heidelberg University, Universitätsklinikum Gießen und Marburg, Humboldt-Universität zu Berlin, Städtisches Klinikum Karlsruhe, Centre Hospitalier Universitaire de Montpellier, Olgahospital, Charité – Universitätsmedizin Berlin
ORCID: 0000-0003-0098-7071
Observed ORCID: 0000-0003-0098-7071
OpenAlex ID: A5034701397
Five novel mutations in steroidogenic factor 1 (SF1,NR5A1) in 46,XY patients with severe underandrogenization but without adrenal insufficiency
2007 · Birgit Köhler, Lin Lin, et al. · Human Mutation · 161
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Severe Hepatotoxicity During Valproate Therapy: An Update and Report of Eight New Fatalities
1994 · A. St. König, H. Siemes, et al. · Epilepsia · 136
Mutations of Genes Involved in the Innate Immune System as Predictors of Sepsis in Very Low Birth Weight Infants
2004 · Peter Ahrens, Evelyn Kattner, et al. · Pediatric Research · 129
Depression as a Risk Factor for Mortality in Individuals with Diabetes: A Meta-Analysis of Prospective Studies
2013 · Mareike Hofmann, Birgit Köhler, et al. · PLoS ONE · 110
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Interferon alpha-2a therapy in haemangiomas of infancy: spastic diplegia as a severe complication
1999 · H. Wörle, E. Maass, et al. · European Journal of Pediatrics · 66
Transient congenital hypothyroidism and hyperthyrotropinemia: normal thyroid function and physical development at the ages of 6-14 years.
1996 · B Köhler, D Schnabel, et al. · The Journal of Clinical Endocrinology & Metabolism · 64
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
2007 · Birgit Köhler, Anne-Lise Delezoide, et al. · Journal of Molecular Endocrinology · 35
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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
2004 · B Kohler, C Pienkowski, et al. · European Journal of Endocrinology · 30
Screening for mutations of the human thyroid peroxidase gene in patients with congenital hypothyroidism
2009 · A. Grüters, B. Köhler, et al. · Experimental and Clinical Endocrinology & Diabetes · 23
An integrated psychosomatic treatment program for people with diabetes (psy-PAD)
2022 · Hanna Kampling, Birgit Köhler, et al. · Deutsches Ärzteblatt international · 22
Preschool development of very low birth weight children born 1994–1995
2003 · Claudia Hanke, Arnold Lohaus, et al. · European Journal of Pediatrics · 22
A Novel Hemizygous Mutation of MAMLD1 in a Patient with 46,XY Complete Gonadal Dysgenesis
2015 · Inge-Lore Ruiz-Arana, Angela Hübner, et al. · Sexual Development · 20
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Clinical report of 8 patients with 49,XXXXY syndrome: Delineation of the facial gestalt and depiction of the clinical spectrum
2018 · Anna L. Burgemeister, Eva Daumiller, et al. · European Journal of Medical Genetics · 19
Acquired Amegakaryocytic Thrombocytopenic Purpura Progressing into Aplastic Anemia
2017 · Jan Philipp Novotný, Birgit Köhler, et al. · Prague Medical Report · 13
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Rickets in Children Receiving Anticonvulsant Drugs
1988 · H. Hauke, B. Köhler · Springer eBooks · 12
Clinical presentation and genetic variants in patients with autoinflammatory diseases: results from the German GARROD registry
2023 · Norbert Blank, Ina Kötter, et al. · Rheumatology International · 10
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Screening for mutations of the human thyroid peroxidase gene in patients with congenital hypothyroidism
1997 · A. Gruters, B. Kohler, et al. · Early Human Development · 4
[Hallervorden-Spatz syndrome with acanthocytosis].
1989 · B Köhler · PubMed · 3
Wirbelsäulenveränderungen bei Neurofibromatose im Kindesalter
1989 · B. Köhler, H. Hauke · RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren · 3
Behandlung eines Patienten mit Diabetes mellitus Typ 2 und einer depressiven Störung
2014 · B. Köhler, J. Kruse · DMW - Deutsche Medizinische Wochenschrift · 2
Sympathische Reflexdystrophie (complex regional pain syndrome type 1), ein im Kindesalter selten diagnostiziertes Schmerzverstärkungssyndrom
2003 · W. Knirsch, M. Holder, et al. · Monatsschrift Kinderheilkunde · 1
Episodic conjugated upward deviation of gaze during early infancy
1997 · H. Wörle, K. Marquard, et al. · Monatsschrift Kinderheilkunde · 1
Die Stuttgarter Neurofibromatose-Studie: Erfahrungen an 72 Kindern mit Morbus Recklinghausen
1989 · B. Köhler · Springer eBooks · 1
Health economic evaluation of “A multidisciplinary psychosocial treatment approach for patients with diabetes (psy-PAD)”
2021 · Clemens Wergen, Charalabos-Markos Dintsios, et al. · Journal of Psychosomatic Research
Genotype-phenotype Analysis of NR5A1/SF1 Mutations by Functional in vitro Studies
2016 · Rebekka Astudillo, Anu Bashamboo, et al. · 55th ESPE Meeting
Works count: 31
Citation count: 887
H-index: 13
I10-index: 16
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