Detlef Böhm

996 total citations
14 papers, 289 citations indexed

About

Detlef Böhm is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Detlef Böhm has authored 14 papers receiving a total of 289 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Reproductive Medicine. Recurrent topics in Detlef Böhm's work include Genomic variations and chromosomal abnormalities (6 papers), Sperm and Testicular Function (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Detlef Böhm is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Sperm and Testicular Function (5 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Detlef Böhm collaborates with scholars based in Germany, United States and Netherlands. Detlef Böhm's co-authors include Jürgen Kohlhase, Wolfgang Engel, Andreas Meinhardt, Ibrahim M. Adham, Karim Nayernia, Stephan Wolf, Dietmar Schlößer, Wiktor Borozdin, Charles Junghanns and Martin von Bergen� and has published in prestigious journals such as Applied Microbiology and Biotechnology, Biology of Reproduction and Molecular and Cellular Endocrinology.

In The Last Decade

Detlef Böhm

14 papers receiving 282 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Detlef Böhm Germany	9	144	127	59	41	32	14	289
Tokuko Iwamori Japan	13	261 1.8×	130 1.0×	13 0.2×	74 1.8×	7 0.2×	28	439
Saravanapriah Nadarajan United States	13	454 3.2×	77 0.6×	56 0.9×	10 0.2×	13 0.4×	16	641
Karen M. Berkowitz United States	7	128 0.9×	90 0.7×	22 0.4×	82 2.0×	45 1.4×	10	258
Tsunetoshi Nakatani Japan	11	323 2.2×	67 0.5×	72 1.2×	13 0.3×	26 0.8×	18	402
Mireille Marsolais Canada	9	208 1.4×	19 0.1×	22 0.4×	33 0.8×	15 0.5×	20	307
Xinran Cheng China	12	207 1.4×	77 0.6×	226 3.8×	11 0.3×	6 0.2×	39	447
Heather Talbott United States	10	65 0.5×	68 0.5×	16 0.3×	93 2.3×	18 0.6×	14	309
Seon-Yong Jeong South Korea	8	211 1.5×	66 0.5×	7 0.1×	5 0.1×	14 0.4×	14	330
А. А. Кашеварова Russia	10	180 1.3×	162 1.3×	58 1.0×	7 0.2×	108 3.4×	51	287
Caixia Li China	13	213 1.5×	293 2.3×	46 0.8×	13 0.3×	8 0.3×	43	435

Countries citing papers authored by Detlef Böhm

Since Specialization

Citations

This map shows the geographic impact of Detlef Böhm'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 Detlef Böhm with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Detlef Böhm more than expected).

Fields of papers citing papers by Detlef Böhm

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Detlef Böhm. 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 Detlef Böhm. The network helps show where Detlef Böhm may publish in the future.

Co-authorship network of co-authors of Detlef Böhm

This figure shows the co-authorship network connecting the top 25 collaborators of Detlef Böhm. A scholar is included among the top collaborators of Detlef Böhm 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 Detlef Böhm. Detlef Böhm is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

Basel‐Vanagaite, Lina, et al.. (2011). An Emerging 1q21.1 Deletion-Associated Neurodevelopmental Phenotype. Journal of Child Neurology. 26(1). 113–116. 18 indexed citations

Ala‐Mello, Sirpa, E. Jaakkola, Jürgen Kohlhase, et al.. (2010). Array CGH in molecular diagnosis of mental retardation—A study of 150 Finnish patients. American Journal of Medical Genetics Part A. 152A(6). 1398–1410. 32 indexed citations

Junghanns, Charles, Marek J. Pecyna, Detlef Böhm, et al.. (2009). Biochemical and molecular genetic characterisation of a novel laccase produced by the aquatic ascomycete Phoma sp. UHH 5-1-03. Applied Microbiology and Biotechnology. 84(6). 1095–1105. 44 indexed citations

Lehnen, H, et al.. (2009). Severe Phenotype in a Girl with Partial Tetrasomy 7, Karyotype 46,XX,trp(7)(q35q36). Cytogenetic and Genome Research. 125(3). 248–252. 5 indexed citations

Shirneshan, Katayoon, Stefan Binder, Detlef Böhm, et al.. (2008). Directed overexpression of insulin in Leydig cells causes a progressive loss of germ cells. Molecular and Cellular Endocrinology. 295(1-2). 79–86. 11 indexed citations

Schubert, Stephanie, Kenji Kamino, Detlef Böhm, et al.. (2008). TSPY Expression Is Variably Altered in Transgenic Mice with Testicular Feminization1. Biology of Reproduction. 79(1). 125–133. 7 indexed citations

Dev, Arvind, Andreas Meinhardt, Dirk G. de Rooij, et al.. (2007). Asthenoteratozoospermia in mice lacking testis expressed gene 18 (Tex18). Molecular Human Reproduction. 13(3). 155–163*. 8 indexed citations

Borozdin, Wiktor, John M. Graham, Detlef Böhm, et al.. (2007). Multigene deletions on chromosome 20q13.13-q13.2 includingSALL4 result in an expanded phenotype of Okihiro syndrome plus developmental delay. Human Mutation. 28(8). 830–830. 42 indexed citations

Sauter, Simone M., Detlef Böhm, Iris Bartels, et al.. (2007). Partial trisomy of distal 19q detected by quantitative real‐time PCR and FISH in a girl with mild facial dysmorphism, hypotonia and developmental delay. American Journal of Medical Genetics Part A. 143A(10). 1091–1099. 9 indexed citations

10.

Böhm, Detlef, Kirsten Hoffmann, Franco Laccone, et al.. (2006). Association of Jacobsen syndrome and bipolar affective disorder in a patient with a de novo 11q terminal deletion. American Journal of Medical Genetics Part A. 140A(4). 378–382. 15 indexed citations

11.

Topaloglu, Özlem, Andreas Meinhardt, Arvind Dev, et al.. (2006). Premature translation of transition protein 2 mRNA causes sperm abnormalities and male infertility. Molecular Reproduction and Development. 74(3). 273–279. 47 indexed citations

12.

Böhm, Detlef. (2002). Disruption of PLC-$beta;1-Mediated Signal Transduction in Mutant Mice Causes Age-Dependent Hippocampal Mossy Fiber Sprouting and Neurodegeneration. Molecular and Cellular Neuroscience. 21(4). 584–601. 42 indexed citations

13.

Nayernia, Karim, et al.. (2001). Isolation and characterization of differentially expressed genes in invasive and non-invasive immortalized murine male germ cells in vitro. International Journal of Oncology. 18(3). 567–74. 8 indexed citations

14.

Nayernia, Karim, Detlef Böhm, Özlem Topaloglu, Gregor Schlüter, & Wolfgang Engel. (2001). Rat transition nuclear protein 2 regulatory region directs haploid expression of reporter gene in male germ cells of transgenic mice. Molecular Reproduction and Development. 58(4). 368–375. 1 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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