Mohammad Mahdi Motazacker

Author

Amsterdam UMC Location University of Amsterdam

Also Known As

M. M. Motazacker, M. Mahdi Motazacker, M. Motazacker, M.M. Motazacker, M. Mahdi Motazacker, Mohammad M. Motazacker, Mohammad Mahdi Motazacker, Mohammad M. Motazacker, Motazacker, Mohammad Mahdi

Publications

1.9K

Citations

H-Index

Concepts

All Affiliations

Amsterdam UMC Location University of Amsterdam Max Planck Institute for Molecular Genetics University of Social Welfare and Rehabilitation Sciences University Medical Center Groningen University of Amsterdam

About

Mohammad Mahdi Motazacker is an author at Amsterdam UMC Location University of Amsterdam specializing in medicine, genetics, and atherosclerosis.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	963
2	Social Sciences	2	2	198
3	Health Sciences	1	1	86
4	Natural Sciences	1	1	49
5	Public Health	1	1	36

Mohammad Mahdi Motazacker

Publications

1.9K

Citations

H-Index

Page 1

	Year	Citations
Genetic Variant of the Scavenger Receptor BI in Humans Menno Vergeer, Suzanne J.A. Korporaal, Remco Franssen, New England Journal of Medicine	2011	305
Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability Lia Abbasi‐Moheb, Sara Mertel, Melanie Gonsior, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsFragile X SpectrumDisease Gene Identification	2012	269
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders Vincenzo Salpietro, Christine L. Dixon, Hui Guo, Nature Communications	2019	236
A Defect in the Ionotropic Glutamate Receptor 6 Gene (GRIK2) Is Associated with Autosomal Recessive Mental Retardation Mohammad Mahdi Motazacker, Benjamin R. Rost, Tim Hucho, The American Journal of Human Genetics NeuropsychologyMolecular NeurosciencePsychiatryGenetic DisorderGenetics	2007	158
Proteome of human plasma very low-density lipoprotein and low-density lipoprotein exhibits a link with coagulation and lipid metabolism Monireh Dashty, Mohammad Mahdi Motazacker, Johannes H.M. Levels, Thrombosis and Haemostasis	2014	109
Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci Hossein Najmabadi, Mohammad Mahdi Motazacker, Masoud Garshasbi, Human Genetics Identifies 8Mendelian DisorderGenetic DisorderMedicineGenetics	2006	103
Heterozygosity for a Loss-of-Function Mutation in GALNT2 Improves Plasma Triglyceride Clearance in Man Adriaan G. Holleboom, Helén Karlsson, Ruei-Shiuan Lin, Cell Metabolism Metabolic SyndromeLipid DisorderLoss-of-function MutationBiochemistryGenetics	2011	99
Advances in genetics show the need for extending screening strategies for autosomal dominant hypercholesterolaemia Mohammad Mahdi Motazacker, James P. Pirruccello, Roeland Huijgen, European Heart Journal	2012	87
Plasma levels of sphingosine-1-phosphate and apolipoprotein M in patients with monogenic disorders of HDL metabolism Ratna Karuna, Rebekka Park, Alaa Othman, Atherosclerosis Metabolic SyndromeLipid DisorderMetabolic DisorderPlasma LevelsLipid Disorders	2011	86
SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly Masoud Garshasbi, Mohammad Mahdi Motazacker, Kimia Kahrizi, Human Genetics Developmental BiologyMendelian DisorderBrain DevelopmentGenetic DisorderGenetics	2005	73

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