Maria M Alves

ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 6

Top Venues

PLoS genetics

Human mutation

EMBO reports

Human molecular genetics

Erasmus Medical Center

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Erasmus Medical Center Mar 01 2012

Netherlands

Senior Scientist :: Clinical Genetics

Publications

Jonathan D Windster, Andrea Sacchetti, Gerben J Schaaf, Eric M J Bindels, Robert Mw Hofstra, Rene Mh Wijnen, Cornelius Ej Sloots, Maria M Alves
A combinatorial panel for flow cytometry-based isolation of enteric nervous system cells from human intestine. EMBO reports (2023)
Almira Zada, Yuying Zhao, Danny Halim, Jonathan Windster, Herma C van der Linde, Jackleen Glodener, Sander Overkleeft, Bianca M de Graaf, Robert M Verdijk, Alice S Brooks, Iain Shepherd, Ya Gao, Alan J Burns, Robert M W Hofstra, Maria M Alves
The long Filamin-a isoform is required for intestinal development and motility: implications for chronic intestinal pseudo-obstruction. Human molecular genetics (2022)
Nathalie Vaes, Musa Idris, Werend Boesmans, Maria M Alves, Veerle Melotte
Nerves in gastrointestinal cancer: from mechanism to modulations. Nature reviews. Gastroenterology & hepatology 19 (12) (2022)
Laura E Kuil, Katherine C MacKenzie, Clara Sze Man Tang, Jonathan D Windster, Thuy Linh Le, Anwarul Karim, Bianca M de Graaf, Robert van der Helm, Yolande van Bever, Cornelius E J Sloots, Conny Meeussen, Dick Tibboel, Annelies de Klein, René M H Wijnen, Jeanne Amiel, Stanislas Lyonnet, Maria-Mercè Garcia-Barcelo, Paul K H Tam, Maria M Alves, Alice S Brooks, Robert M W Hofstra, Erwin Brosens
Size matters: Large copy number losses in Hirschsprung disease patients reveal genes involved in enteric nervous system development. PLoS genetics 17 (8) (2021)
Katherine C MacKenzie, Rhiana Garritsen, Rajendra K Chauhan, Yunia Sribudiani, Bianca M de Graaf, Tim Rugenbrink, Rutger Brouwer, Wilfred F J van Ijcken, Ivo de Blaauw, Alice S Brooks, Cornelius E J Sloots, Conny J H M Meeuwsen, René M Wijnen, Donald F Newgreen, Alan J Burns, Robert M W Hofstra, Maria M Alves, Erwin Brosens
The Somatic Mutation Paradigm in Congenital Malformations: Hirschsprung Disease as a Model. International journal of molecular sciences 22 (22) (2021)
Katherine C MacKenzie, Bianca M de Graaf, Andreas Syrimis, Yuying Zhao, Erwin Brosens, Grazia M S Mancini, Rachel Schot, Dicky Halley, Martina Wilke, Arve Vøllo, Frances Flinter, Andrew Green, Sahar Mansour, Jacek Pilch, Zornitza Stark, Eleni Zamba-Papanicolaou, Violetta Christophidou-Anastasiadou, Robert M W Hofstra, Jan D H Jongbloed, Nayia Nicolaou, George A Tanteles, Alice S Brooks, Maria M Alves
Goldberg-Shprintzen syndrome is determined by the absence, or reduced expression levels, of KIFBP. Human mutation 41 (11) (2020)

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Publication Activity (10 Years)

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Maria M Alves