Birgit Köhler

1.2k total citations
21 papers, 675 citations indexed

About

Birgit Köhler is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Birgit Köhler has authored 21 papers receiving a total of 675 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Endocrinology, Diabetes and Metabolism and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Birgit Köhler's work include Diabetes Management and Education (3 papers), Renal and related cancers (3 papers) and Sexual Differentiation and Disorders (3 papers). Birgit Köhler is often cited by papers focused on Diabetes Management and Education (3 papers), Renal and related cancers (3 papers) and Sexual Differentiation and Disorders (3 papers). Birgit Köhler collaborates with scholars based in Germany, United States and France. Birgit Köhler's co-authors include Dorothee Kaudewitz, Hanns‐Martin Lorenz, Annette Grüters, Heike Biebermann, Dirk Schnabel, Johannes Kruse, Falk Leichsenring, Mareike Hofmann, E Kattner and Wolfgang Göpel and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Toxicology.

In The Last Decade

Birgit Köhler

19 papers receiving 653 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Birgit Köhler Germany 12 239 145 134 114 110 21 675
Toshihide Kubo Japan 17 178 0.7× 99 0.7× 174 1.3× 45 0.4× 83 0.8× 48 748
Emõke Endreffy Hungary 16 141 0.6× 104 0.7× 47 0.4× 121 1.1× 111 1.0× 38 693
R. Tenaglia Italy 18 331 1.4× 274 1.9× 71 0.5× 57 0.5× 69 0.6× 64 841
Adrienne H. Williams United States 18 229 1.0× 369 2.5× 190 1.4× 228 2.0× 191 1.7× 27 1.1k
J. Scott Gabrielsen United States 13 221 0.9× 49 0.3× 58 0.4× 50 0.4× 37 0.3× 23 826
Heike Goebel Germany 14 184 0.8× 65 0.4× 68 0.5× 377 3.3× 27 0.2× 29 1.0k
Damien C. Croteau‐Chonka United States 14 278 1.2× 238 1.6× 26 0.2× 127 1.1× 45 0.4× 25 755
Jingzhou Wang China 14 169 0.7× 156 1.1× 36 0.3× 132 1.2× 35 0.3× 44 641
Cong-Lin Liu United States 15 247 1.0× 156 1.1× 31 0.2× 226 2.0× 46 0.4× 21 913
Humberto Garcia‐Ortíz Mexico 14 152 0.6× 134 0.9× 55 0.4× 115 1.0× 65 0.6× 36 506

Countries citing papers authored by Birgit Köhler

Since Specialization
Citations

This map shows the geographic impact of Birgit Köhler's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Birgit Köhler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Birgit Köhler more than expected).

Fields of papers citing papers by Birgit Köhler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Birgit Köhler. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Birgit Köhler. The network helps show where Birgit Köhler may publish in the future.

Co-authorship network of co-authors of Birgit Köhler

This figure shows the co-authorship network connecting the top 25 collaborators of Birgit Köhler. A scholar is included among the top collaborators of Birgit Köhler based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Birgit Köhler. Birgit Köhler is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Blank, Norbert, Ina Kötter, Marc Schmalzing, et al.. (2023). Clinical presentation and genetic variants in patients with autoinflammatory diseases: results from the German GARROD registry. Rheumatology International. 44(2). 263–271. 6 indexed citations
2.
Kampling, Hanna, Birgit Köhler, Burkhard Haastert, et al.. (2022). An integrated psychosomatic treatment program for people with diabetes (psy-PAD). Deutsches Ärzteblatt international. 119(14). 245–252. 7 indexed citations
3.
Köhler, Birgit, et al.. (2019). Current Therapeutic Options in the Treatment of Rheumatoid Arthritis. Journal of Clinical Medicine. 8(7). 938–938. 153 indexed citations
4.
Köhler, Birgit, Hanns‐Martin Lorenz, & Norbert Blank. (2018). IL1-blocking therapy in colchicine-resistant familial Mediterranean fever. European Journal of Rheumatology. 5(4). 230–234. 27 indexed citations
5.
Graul‐Neumann, Luitgard, et al.. (2018). Clinical report of 8 patients with 49,XXXXY syndrome: Delineation of the facial gestalt and depiction of the clinical spectrum. European Journal of Medical Genetics. 62(3). 210–216. 12 indexed citations
6.
Novotný, Jan, Birgit Köhler, Regina Max, & Gerlinde Egerer. (2017). Acquired Amegakaryocytic Thrombocytopenic Purpura Progressing into Aplastic Anemia. Prague Medical Report. 118(4). 147–155. 8 indexed citations
7.
Hübner, Angela, Heiko Krude, Annette Grüters, et al.. (2015). A Novel Hemizygous Mutation of <b><i>MAMLD1</i></b> in a Patient with 46,XY Complete Gonadal Dysgenesis. Sexual Development. 9(2). 80–85. 15 indexed citations
8.
Köhler, Birgit & Johannes Kruse. (2014). Behandlung eines Patienten mit Diabetes mellitus Typ 2 und einer depressiven Störung. DMW - Deutsche Medizinische Wochenschrift. 139(12). 592–595.
9.
Hofmann, Mareike, Birgit Köhler, Falk Leichsenring, & Johannes Kruse. (2013). Depression as a Risk Factor for Mortality in Individuals with Diabetes: A Meta-Analysis of Prospective Studies. PLoS ONE. 8(11). e79809–e79809. 85 indexed citations
10.
Grüters, Annette, Birgit Köhler, Annika Wolf, et al.. (2009). Screening for mutations of the human thyroid peroxidase gene in patients with congenital hypothyroidism. Experimental and Clinical Endocrinology & Diabetes. 104(S 04). 121–123. 7 indexed citations
11.
Köhler, Birgit, Lin Lin, Bruno Ferraz‐de‐Souza, et al.. (2007). Five novel mutations in steroidogenic factor 1 (SF1,NR5A1) in 46,XY patients with severe underandrogenization but without adrenal insufficiency. Human Mutation. 29(1). 59–64. 106 indexed citations
12.
Schümann, Klaus, et al.. (2007). A method to assess 59Fe in residual tissue blood content in mice and its use to correct 59Fe-distribution kinetics accordingly. Toxicology. 241(1-2). 19–32. 25 indexed citations
13.
Ahrens, Peter, E Kattner, Birgit Köhler, et al.. (2004). Mutations of Genes Involved in the Innate Immune System as Predictors of Sepsis in Very Low Birth Weight Infants. Pediatric Research. 55(4). 652–656. 100 indexed citations
14.
Köhler, Birgit, Catherine Pienkowski, Martine Delsol, et al.. (2004). 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. European Journal of Endocrinology. 150(6). 825–830. 25 indexed citations
15.
Lohaus, Arnold, et al.. (2003). Preschool development of very low birth weight children born 1994–1995. European Journal of Pediatrics. 162(3). 159–164. 14 indexed citations
16.
17.
Grüters, Annette, Birgit Köhler, Annika Wolf, et al.. (1997). Screening for mutations of the human thyroid peroxidase gene in patients with congenital hypothyroidism. Early Human Development. 49(1). 76–76. 4 indexed citations
18.
Marquard, Klaus, et al.. (1997). Episodic conjugated upward deviation of gaze during early infancy. Monatsschrift Kinderheilkunde. 145(6). 602–605. 1 indexed citations
19.
Köhler, Birgit, Dirk Schnabel, Heike Biebermann, & Annette Grüters. (1996). Transient congenital hypothyroidism and hyperthyrotropinemia: normal thyroid function and physical development at the ages of 6-14 years.. The Journal of Clinical Endocrinology & Metabolism. 81(4). 1563–1567. 53 indexed citations
20.
Köhler, Birgit. (1989). [Hallervorden-Spatz syndrome with acanthocytosis].. PubMed. 137(9). 616–9. 2 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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