Martin Becker

1.2k total citations
15 papers, 823 citations indexed

About

Martin Becker is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Martin Becker has authored 15 papers receiving a total of 823 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Martin Becker's work include Genetic factors in colorectal cancer (3 papers), Autism Spectrum Disorder Research (3 papers) and Genomics and Rare Diseases (2 papers). Martin Becker is often cited by papers focused on Genetic factors in colorectal cancer (3 papers), Autism Spectrum Disorder Research (3 papers) and Genomics and Rare Diseases (2 papers). Martin Becker collaborates with scholars based in Sweden, United States and Australia. Martin Becker's co-authors include Martin Fishbein, Pico Caroni, Richard P. Barth, Simon J. Leedham, Hayley L. Belnoue-Davis, Ian Tomlinson, Annabelle Lewis, Emma Jaeger, James E. East and Huw Thomas and has published in prestigious journals such as Nature Genetics, Journal of Neuroscience and Gastroenterology.

In The Last Decade

Martin Becker

15 papers receiving 782 citations

Peers

Countries citing papers authored by Martin Becker

Since Specialization

Citations

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

Fields of papers citing papers by Martin Becker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Becker

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Screening autism-associated environmental factors in differentiating human neural progenitors with fractional factorial design-based transcriptomics 2023 ·Scientific Reports ·(unknown), Martin Becker, (unknown), (unknown), Danyang Li, Francesca Mastropasqua, Michelle Watts, Manish Arora, Anna Falk, (unknown), Ingela Lanekoff, Kristiina Tammimies	3
2	Spermatogonia Loss Correlates with LAMA 1 Expression in Human Prepubertal Testes Stored for Fertility Preservation 2021 ·Cells ·(unknown), Elisabet Åkesson, Masahito Yoshihara, Elizabeth Oliver, Yanhua Cui, Martin Becker, João Pedro Alves-Lopes, Ragnar Bjarnason, Patrik Romerius, Mikael Sundin, (unknown), Cecilia Langenskiöld, Hartmut Vogt, Lars Henningsohn, Cecilia Petersen, Olle Söder, Jingtao Guo, Rod T. Mitchell, Kirsi Jahnukainen, Jan‐Bernd Stukenborg	22
3	Rare variants in the outcome of social skills group training for autism 2021 ·Autism Research ·Danyang Li, Nora Choque Olsson, Martin Becker, (unknown), Hong Jiao, (unknown), Ulf Jönsson, Sven Bölte, Kristiina Tammimies	6
4	Presynaptic dysfunction in CASK-related neurodevelopmental disorders 2020 ·Translational Psychiatry ·Martin Becker, Francesca Mastropasqua, (unknown), Simon Maier, Mai‐Lan Ho, (unknown), Danyang Li, Janina Neufeld, (unknown), (unknown), (unknown), (unknown), Josephine Wincent, Charlotte Willfors, Rouslan Sitnikov, Eric Herlenius, Britt‐Marie Anderlid, Anna Falk, Sven Bölte, Kristiina Tammimies	22
5	Association between Copy Number Variation and Response to Social Skills Training in Autism Spectrum Disorder 2019 ·Scientific Reports ·Kristiina Tammimies, Danyang Li, (unknown), (unknown), Martin Becker, (unknown), Steve Berggren, Christina Coco, Torbjörn Falkmer, Ulf Jönsson, Nora Choque Olsson, Sven Bölte	11
6	Mapping of Human FOXP2 Enhancers Reveals Complex Regulation 2018 ·Frontiers in Molecular Neuroscience ·Martin Becker, Paolo Devanna, Simon E. Fisher, Sonja C. Vernes	19
7	Enrichment of rare copy number variation in children with developmental language disorder 2018 ·Clinical Genetics ·(unknown), (unknown), Myriam Peyrard‐Janvid, (unknown), Martin Becker, Torkel Klingberg, Juha Kere, Hans Forssberg, Kristiina Tammimies	17
8	Early developmental gene enhancers affect subcortical volumes in the adult human brain 2016 ·Human Brain Mapping ·Martin Becker, Tulio Guadalupe, Barbara Franke, Derrek P. Hibar, Miguel E. Rentería, Jason L. Stein, Paul M. Thompson, Clyde Francks, Sonja C. Vernes, Simon E. Fisher	4
9	A chromosomal rearrangement in a child with severe speech and language disorder separates FOXP2 from a functional enhancer 2015 ·Molecular Cytogenetics ·Martin Becker, Paolo Devanna, Simon E. Fisher, Sonja C. Vernes	9
10	A Polymorphic Enhancer near GREM1 Influences Bowel Cancer Risk through Differential CDX2 and TCF7L2 Binding 2014 ·Cell Reports ·Annabelle Lewis, Luke Freeman-Mills, Elisa de la Calle‐Mustienes, Rosa M. Giráldez‐Pérez, Hayley L. Belnoue-Davis, Emma Jaeger, Martin Becker, Nina C. Hubner, Luan N. Nguyen, Jorge Zerón-Medina, (unknown), Hendrik G. Stunnenberg, Jaime J. Carvajal, José Luis Gómez-Skármeta, Simon J. Leedham, Ian Tomlinson	34
11	Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP antagonist GREM1 2012 ·Nature Genetics ·Emma Jaeger, Simon J. Leedham, Annabelle Lewis, Stefania Segditsas, Martin Becker, (unknown), Hayley L. Belnoue-Davis, Kulvinder Kaur, Karl Heinimann, Kimberley Howarth, James E. East, Jenny C. Taylor, Huw Thomas, Ian Tomlinson	160
12	551 Hereditary Mixed Polyposis Syndrome is Caused by a 40kb Upstream Duplication That Leads to Increased and Ectopic Expression of the BMP Antagonist Grem1 2012 ·Gastroenterology ·Simon J. Leedham, (unknown), Annabelle Lewis, Stefania Segditsas, Martin Becker, James E. East, Jenny C. Taylor, Huw Thomas, Ian Tomlinson	4
13	Factors influencing behavior and behavior change. 2000 ·Martin Fishbein, (unknown), (unknown), Martin Becker, (unknown)	377
14	Power through choices: the development of a sexuality education curriculum for youths in out-of-home care. 2000 ·PubMed ·Martin Becker, Richard P. Barth	37
15	The downregulation of growth-associated proteins in motoneurons at the onset of synapse elimination is controlled by muscle activity and IGF1 1992 ·Journal of Neuroscience ·Pico Caroni, Martin Becker	98

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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