Maarten P.G. Massink

Author

Also Known As

Bernabeu, Carmelo, Jane A Hurst, M. M. G. MASSINK, Maarten Massink, Maarten P G Massink, Maarten P. G. Massink, Maarten P.G. Massink, Maarten PG Massink, Maarten Pieter Gerrit Massink, Maarten P.G. Massink

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

University Medical Center Utrecht Amsterdam UMC Location Vrije Universiteit Amsterdam Amsterdam UMC Location University of Amsterdam Utrecht University Erasmus MC

About

Maarten P.G. Massink is an author at University Medical Center Utrecht specializing in medicine, cell biology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	360
2	Cell Biology	3	3	213
3	Engineering	1	1	32
4	Anatomy	1	1	32
5	Biomedical Engineering	1	1	32

Maarten P.G. Massink

Publications

954

Citations

H-Index

Page 1

	Year	Citations
Intestinal Failure and Aberrant Lipid Metabolism in Patients With DGAT1 Deficiency Jorik M. van Rijn, Rico Chandra Ardy, Zarife Kuloğlu, Gastroenterology	2018	116
Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia Maarten P.G. Massink, Marijn Créton, Francesca Spanevello, The American Journal of Human Genetics Signal TransductionDevelopmental BiologyGenetic DisorderGeneticsReceptor (Biochemistry)	2015	115
Somatic genomic alterations in retinoblastoma beyond RB1 are rare and limited to copy number changes Irsan Kooi, Berber M. Mol, Maarten P.G. Massink, Scientific Reports GeneticsPathologyMolecular GeneticsSomatic Genomic AlterationsTumor Biology	2016	111
Genetic obesity: next-generation sequencing results of 1230 patients with obesity Lotte Kleinendorst, Maarten P.G. Massink, Mellody I. Cooiman, Journal of Medical Genetics	2018	104
Genomic profiling of CHEK2*1100delC-mutated breast carcinomas Maarten P.G. Massink, Irsan Kooi, John W.M. Martens, BMC Cancer	2015	75
Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome Anneke J.A. Kievit, Federico Tessadori, Hannie Douben, European Journal of Human Genetics Signal TransductionCadherin–catenin ComplexPathologyDegenerative DiseaseNeuropathology	2018	69
Clonality, Antigen Recognition, and Suppression of CD8+ T Cells Differentially Affect Prognosis of Breast Cancer Subtypes Dora Hammerl, Maarten P.G. Massink, Marcel Smid, Clinical Cancer Research	2019	49
<scp> <i>HNRNPH1</i> </scp> ‐related syndromic intellectual disability: Seven additional cases suggestive of a distinct syndromic neurodevelopmental syndrome Sara L. Reichert, Rachel Li, Scott A. Turner, Clinical Genetics	2020	43
ABCC9-related Intellectual disability Myopathy Syndrome is a KATP channelopathy with loss-of-function mutations in ABCC9 Marie Falkenberg Smeland, Conor McClenaghan, Helen I. Roessler, Nature Communications	2019	40
Comparative analysis of the natriuretic peptide precursor gene cluster in vertebrates reveals loss of ANF and retention of CNP‐3 in chicken Arjan C. Houweling, Semir Somi, Maarten P.G. Massink, Developmental Dynamics	2005	34

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