Ibrahim M. Adham

6.0k total citations · 1 hit paper
95 papers, 4.6k citations indexed

About

Ibrahim M. Adham is a scholar working on Molecular Biology, Public Health, Environmental and Occupational Health and Genetics. According to data from OpenAlex, Ibrahim M. Adham has authored 95 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 36 papers in Public Health, Environmental and Occupational Health and 36 papers in Genetics. Recurrent topics in Ibrahim M. Adham's work include Sperm and Testicular Function (31 papers), Reproductive Biology and Fertility (24 papers) and Animal Genetics and Reproduction (19 papers). Ibrahim M. Adham is often cited by papers focused on Sperm and Testicular Function (31 papers), Reproductive Biology and Fertility (24 papers) and Animal Genetics and Reproduction (19 papers). Ibrahim M. Adham collaborates with scholars based in Germany, Poland and United States. Ibrahim M. Adham's co-authors include Wolfgang Engel, Karim Nayernia, Stephan Zimmermann, Judith M. A. Emmen, Gerd Steding, Albert O. Brinkmann, Andreas Meinhardt, Alexander I. Agoulnik, Adolf F. Holstein and Mohamed Benahmed and has published in prestigious journals such as Nature, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Ibrahim M. Adham

95 papers receiving 4.5k citations

Hit Papers

Targeted Disruption of the Insl3 Gene Causes Bilateral Cr... 1999 2026 2008 2017 1999 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ibrahim M. Adham Germany 39 2.2k 1.9k 1.4k 1.1k 823 95 4.6k
Karim Nayernia Germany 30 1.6k 0.8× 2.7k 1.5× 1.5k 1.1× 1.1k 1.0× 796 1.0× 90 4.5k
Susanna Dolci Italy 37 1.5k 0.7× 2.8k 1.5× 1.7k 1.2× 1.8k 1.5× 621 0.8× 109 4.9k
Will M. Lee Hong Kong 40 1.4k 0.7× 1.6k 0.9× 2.7k 1.9× 583 0.5× 400 0.5× 72 4.0k
Eimei Sato Japan 37 3.2k 1.5× 2.3k 1.3× 1.9k 1.4× 862 0.7× 315 0.4× 270 5.1k
Peter G. Stanton Australia 40 1.4k 0.6× 1.6k 0.9× 2.5k 1.8× 906 0.8× 320 0.4× 124 4.2k
D.M. de Kretser Australia 33 1.0k 0.5× 1.6k 0.8× 1.9k 1.4× 568 0.5× 589 0.7× 68 3.8k
Abraham L. Kierszenbaum United States 39 1.9k 0.9× 2.2k 1.2× 2.7k 2.0× 1.6k 1.4× 289 0.4× 110 4.8k
Kaoru Miyamoto Japan 44 1.3k 0.6× 3.0k 1.6× 1.5k 1.1× 1.4k 1.2× 273 0.3× 172 6.0k
Raffaele Geremia Italy 41 1.5k 0.7× 2.7k 1.5× 2.0k 1.4× 1.4k 1.2× 390 0.5× 99 4.9k
M. Parvinen Finland 38 1.1k 0.5× 1.6k 0.9× 2.2k 1.6× 771 0.7× 480 0.6× 80 3.9k

Countries citing papers authored by Ibrahim M. Adham

Since Specialization
Citations

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

Fields of papers citing papers by Ibrahim M. Adham

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ibrahim M. Adham. 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 Ibrahim M. Adham. The network helps show where Ibrahim M. Adham may publish in the future.

Co-authorship network of co-authors of Ibrahim M. Adham

This figure shows the co-authorship network connecting the top 25 collaborators of Ibrahim M. Adham. A scholar is included among the top collaborators of Ibrahim M. Adham 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 Ibrahim M. Adham. Ibrahim M. Adham 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.
Bochenek, M., et al.. (2023). Increased DNA strand breaks in spermatozoa of Pxt1 knockout mice. Reproduction Fertility and Development. 35(11). 589–600. 1 indexed citations
2.
Barakat, Amal Z., et al.. (2022). Heat shock protein A4 ablation leads to skeletal muscle myopathy associated with dysregulated autophagy and induced apoptosis. Journal of Translational Medicine. 20(1). 229–229. 11 indexed citations
3.
Adham, Ibrahim M., et al.. (2018). Ultra-structure of the sperm head-to-tail linkage complex in the absence of the spermatid-specific LINC component SPAG4. Histochemistry and Cell Biology. 150(1). 49–59. 25 indexed citations
4.
Xu, Xingbo, et al.. (2014). Pelota regulates the development of extraembryonic endoderm through activation of bone morphogenetic protein (BMP) signaling. Stem Cell Research. 13(1). 61–74. 11 indexed citations
5.
Thanasupawat, Thatchawan, Ibrahim M. Adham, Jean‐Eric Ghia, et al.. (2012). INSL5 is a novel marker for human enteroendocrine cells of the large intestine and neuroendocrine tumours. Oncology Reports. 29(1). 149–154. 25 indexed citations
6.
Mohamed, Belal A., Amal Z. Barakat, Wolfram‐Hubertus Zimmermann, et al.. (2012). Targeted disruption of Hspa4 gene leads to cardiac hypertrophy and fibrosis. Journal of Molecular and Cellular Cardiology. 53(4). 459–468. 35 indexed citations
7.
Grzmil, Paweł, J Konietzko, Alicia Aguilar, et al.. (2009). Targeted Disruption of the Mouse <i>Npal3</i> Gene Leads to Deficits in Behavior, Increased IgE Levels, and Impaired Lung Function. Cytogenetic and Genome Research. 125(3). 186–200. 7 indexed citations
8.
Rashid, Sajid, Paweł Grzmil, Jörg‐Detlef Drenckhahn, et al.. (2009). Disruption of the murine dynein light chain gene Tcte3-3 results in asthenozoospermia. Reproduction. 139(1). 99–111. 24 indexed citations
9.
Böhm, Johann, Wiktor Borozdin, Ashraf U. Mannan, et al.. (2008). Sall1, Sall2, and Sall4 Are Required for Neural Tube Closure in Mice. American Journal Of Pathology. 173(5). 1455–1463. 51 indexed citations
10.
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
11.
Pauer, Hans‐Ulrich, Thomas Renné, Bernhard Hemmerlein, et al.. (2004). Targeted deletion of murine coagulation factor XII gene-a model for contact phase activation in vivo. Thrombosis and Haemostasis. 92(9). 503–508. 103 indexed citations
12.
Adham, Ibrahim M.. (2002). The Overexpression of the Insl3 in Female Mice Causes Descent of the Ovaries. Molecular Endocrinology. 16(2). 244–252. 34 indexed citations
13.
Adham, Ibrahim M., et al.. (2002). The Overexpression of theInsl3in Female Mice Causes Descent of the Ovaries. Molecular Endocrinology. 16(2). 244–252. 109 indexed citations
14.
Adham, Ibrahim M., et al.. (2000). Molecular cloning, expression and chromosome location of the human pelota gene PELO. Cytogenetic and Genome Research. 90(1-2). 75–78. 18 indexed citations
15.
Zimmermann, Stephan, Gerd Steding, Judith M. A. Emmen, et al.. (1999). Targeted Disruption of the Insl3 Gene Causes Bilateral Cryptorchidism. Molecular Endocrinology. 13(5). 681–691. 528 indexed citations breakdown →
17.
Rettenberger, G., Ibrahim M. Adham, Wolfgang Engel, C. Klett, & H. Hameister. (1995). Assignment of the porcine acrosin gene, ACR, to Chromosome 5p15 by fluorescence in situ hybridization (FISH). Mammalian Genome. 6(1). 60–61. 6 indexed citations
19.
Luerßen, Hartmut, Marie‐Geneviève Mattéi, Matthias Schröter, et al.. (1990). Nucleotide sequence of the gene for human transition protein 1 and its chromosomal localization on chromosome 2. Genomics. 8(2). 324–330. 49 indexed citations
20.
Adham, Ibrahim M., et al.. (1990). Nucleotide sequence and exon‐intron organization of the human proacrosin gene. European Journal of Biochemistry. 190(1). 195–200. 29 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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