M. Albert Basson

9.0k total citations · 1 hit paper
73 papers, 4.6k citations indexed

About

M. Albert Basson is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, M. Albert Basson has authored 73 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Molecular Biology, 17 papers in Genetics and 13 papers in Genetics. Recurrent topics in M. Albert Basson's work include Fibroblast Growth Factor Research (16 papers), Congenital heart defects research (14 papers) and Epigenetics and DNA Methylation (11 papers). M. Albert Basson is often cited by papers focused on Fibroblast Growth Factor Research (16 papers), Congenital heart defects research (14 papers) and Epigenetics and DNA Methylation (11 papers). M. Albert Basson collaborates with scholars based in United Kingdom, United States and Canada. M. Albert Basson's co-authors include Andrew S. Brack, Jonathan D. Licht, Joe V. Chakkalakal, Rose Zamoyska, Jacqueline M. Mason, D. Morrison, Alex P. A. Donovan, Ivor Mason, Gail R. Martin and Tian Yu and has published in prestigious journals such as Nature, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

M. Albert Basson

72 papers receiving 4.5k citations

Hit Papers

The aged niche disrupts m... 2012 2026 2016 2021 2012 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Albert Basson United Kingdom 34 3.2k 758 514 497 465 73 4.6k
Mustafa Tekin United States 42 3.0k 0.9× 1.5k 1.9× 438 0.9× 669 1.3× 339 0.7× 219 5.5k
Susan H. Blanton United States 43 2.8k 0.9× 2.3k 3.0× 551 1.1× 269 0.5× 411 0.9× 189 6.2k
Leopoldo Zelante Italy 41 3.4k 1.1× 964 1.3× 281 0.5× 181 0.4× 315 0.7× 160 6.5k
Lisbeth Tranebjærg Denmark 43 3.6k 1.1× 2.3k 3.0× 415 0.8× 577 1.2× 349 0.8× 163 6.7k
Lies H. Hoefsloot Netherlands 45 3.7k 1.1× 1.7k 2.3× 772 1.5× 532 1.1× 1.1k 2.5× 136 6.6k
Nicholas Lench United Kingdom 36 2.7k 0.9× 1.3k 1.8× 866 1.7× 259 0.5× 204 0.4× 107 5.5k
Ricardo Pardal Spain 28 4.2k 1.3× 1.0k 1.3× 1.0k 2.0× 342 0.7× 1.1k 2.4× 61 7.6k
Hannie Kremer Netherlands 44 5.1k 1.6× 1.2k 1.5× 654 1.3× 836 1.7× 243 0.5× 188 8.0k
Gudrun Nürnberg Germany 44 2.9k 0.9× 1.6k 2.1× 272 0.5× 524 1.1× 280 0.6× 93 5.1k
Corrinne G. Lobe Canada 31 3.4k 1.1× 871 1.1× 731 1.4× 689 1.4× 331 0.7× 48 5.3k

Countries citing papers authored by M. Albert Basson

Since Specialization
Citations

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

Fields of papers citing papers by M. Albert Basson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Albert Basson

This figure shows the co-authorship network connecting the top 25 collaborators of M. Albert Basson. A scholar is included among the top collaborators of M. Albert Basson 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 M. Albert Basson. M. Albert Basson 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.
Bhatt, S., Talia Gileadi, Enikö A. Kramár, et al.. (2024). The Intellectual Disability Risk GeneKdm5bRegulates Long-Term Memory Consolidation in the Hippocampus. Journal of Neuroscience. 44(19). e1544232024–e1544232024.
2.
Donovan, Alex P. A., Jacob Ellegood, Yushi Redhead, et al.. (2023). Pervasive cortical and white matter anomalies in a mouse model for CHARGE syndrome. Journal of Anatomy. 243(1). 51–65. 2 indexed citations
3.
Xiao, Wenfeng, Muralidhara Rao Maradana, Yajing Gao, et al.. (2023). Aryl hydrocarbon receptor utilises cellular zinc signals to maintain the gut epithelial barrier. Nature Communications. 14(1). 5431–5431. 27 indexed citations
4.
Badodi, Sara, Nicola Pomella, Xinyu Zhang, et al.. (2021). Inositol treatment inhibits medulloblastoma through suppression of epigenetic-driven metabolic adaptation. Nature Communications. 12(1). 2148–2148. 19 indexed citations
5.
Zerbi, Valerio, Marco Pagani, Marija Markicevic, et al.. (2021). Brain mapping across 16 autism mouse models reveals a spectrum of functional connectivity subtypes. Molecular Psychiatry. 26(12). 7610–7620. 57 indexed citations
6.
Ramaswamy, Vijay, Marcel Kool, Brigitta Stockinger, et al.. (2020). The AHR pathway represses TGFβ-SMAD3 signalling and has a potent tumour suppressive role in SHH medulloblastoma. Scientific Reports. 10(1). 148–148. 20 indexed citations
7.
Basson, M. Albert, et al.. (2018). Autism‐linked CHD gene expression patterns during development predict multi‐organ disease phenotypes. Journal of Anatomy. 233(6). 755–769. 11 indexed citations
8.
Donovan, Alex P. A., Jacob Ellegood, Holger A. Volk, et al.. (2017). Distinct cerebellar foliation anomalies in a CHD7 haploinsufficient mouse model of CHARGE syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 175(4). 18 indexed citations
9.
Howe, Kathy, David J. Price, John O. Mason, et al.. (2014). Heparan Sulfotransferases Hs6st1 and Hs2st Keep Erk in Check for Mouse Corpus Callosum Development. Journal of Neuroscience. 34(6). 2389–2401. 26 indexed citations
10.
Basson, M. Albert, et al.. (2012). Sprouty Is a Negative Regulator of Transforming Growth Factor β-Induced Epithelial-to-Mesenchymal Transition and Cataract. Molecular Medicine. 18(5). 861–873. 45 indexed citations
11.
Magnani, Dario, Kerstin Hasenpusch‐Theil, Carine Benadiba, et al.. (2012). Gli3 Controls Corpus Callosum Formation by Positioning Midline Guideposts During Telencephalic Patterning. Cerebral Cortex. 24(1). 186–198. 28 indexed citations
12.
Mao, Yaopan, Joanna F. Mulvaney, Sana Zakaria, et al.. (2011). Characterization of a Dchs1 mutant mouse reveals requirements for Dchs1-Fat4 signaling during mammalian development. Development. 138(5). 947–957. 164 indexed citations
13.
Macià, Anna, Marı́a Santacana, Agnieszka Maliszewska, et al.. (2011). Sprouty1 is a candidate tumor-suppressor gene in medullary thyroid carcinoma. Oncogene. 31(35). 3961–3972. 30 indexed citations
14.
Yaguchi, Yuichiro, Tian Yu, Mohi Ahmed, et al.. (2009). Fibroblast growth factor (FGF) gene expression in the developing cerebellum suggests multiple roles for FGF signaling during cerebellar morphogenesis and development. Developmental Dynamics. 238(8). 2058–2072. 38 indexed citations
15.
McCue, Karen, Catherine Roberts, Vanessa Kyriakopoulou, et al.. (2009). Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice. Journal of Clinical Investigation. 119(11). 3301–10. 111 indexed citations
16.
Basson, M. Albert, T. Wilson, Giuseppe Legname, et al.. (2000). Early Growth Response (Egr)-1 Gene Induction in the Thymus in Response to TCR Ligation During Early Steps in Positive Selection Is Not Required for CD8 Lineage Commitment. The Journal of Immunology. 165(5). 2444–2450. 22 indexed citations
17.
Basson, M. Albert & Rose Zamoyska. (2000). The CD4/CD8 lineage decision: integration of signalling pathways. Immunology Today. 21(10). 509–514. 35 indexed citations
18.
Mee, P. Joseph, Martin Turner, M. Albert Basson, et al.. (1999). Greatly reduced efficiency of both positive and negative selection of thymocytes in CD45 tyrosine phosphatase-deficient mice. European Journal of Immunology. 29(9). 2923–2933. 60 indexed citations
19.
Bommhardt, Ursula, et al.. (1999). Activation of the Extracellular Signal-Related Kinase/Mitogen-Activated Protein Kinase Pathway Discriminates CD4 Versus CD8 Lineage Commitment in the Thymus. The Journal of Immunology. 163(2). 715–722. 75 indexed citations
20.
Basson, M. Albert, Ursula Bommhardt, Michael S. Cole, J. Yun Tso, & Rose Zamoyska. (1998). CD3 Ligation on Immature Thymocytes Generates Antagonist-like Signals Appropriate for CD8 Lineage Commitment, Independently of  T Cell Receptor Specificity. The Journal of Experimental Medicine. 187(8). 1249–1260. 54 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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