Nader Chalhoub - Concepedia

Author

Nader Chalhoub

Weill Cornell Medical College in Qatar

Also Known As

Chalhoub, Nader, N Chalhoub, N. Chalhoub, Nader Chalhoub

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

Weill Cornell Medical College in Qatar Hamad Medical Corporation Cornell University St. Jude Children's Research Hospital MIND Research Institute

About

Nader Chalhoub is an author at Weill Cornell Medical College in Qatar specializing in medicine, cell biology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	536
2	Cell Biology	4	4	233
3	Social Sciences	2	2	96
4	Molecular Genetics	1	1	83
5	Neurology	1	1	74

Nader Chalhoub

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Novel mutations target distinct subgroups of medulloblastoma Giles Robinson, Matthew Parker, Tanya A. Kranenburg, Nature	2012	845
Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human Nader Chalhoub, Nadia Benachenhou, Venkatesh Rajapurohitam, Nature Medicine Bone DiseaseSclerostinDevelopmental BiologyBone Morphogenic ProteinGenetic Disorder	2003	265
Mutation in noncoding <scp>RNA RNU12</scp> causes early onset cerebellar ataxia Mahmoud F. Elsaid, Nader Chalhoub, Tawfeg Ben‐Omran, Annals of Neurology	2016	89
Recurrent genomic alterations characterize medulloblastoma arising from DNA double-strand break repair deficiency Pierre‐Olivier Frappart, Youngsoo Lee, H. R. Russell, Proceedings of the National Academy of Sciences Recurrent Genomic AlterationsGeneticsPathologyMolecular GeneticsDisease Gene Identification	2009	83
Cell type specificity of PI3K signaling in Pdk1- and Pten-deficient brains Nader Chalhoub, Guo Zhu, Xiaoyan Zhu, Genes & Development Cell DeathPten-deficient BrainsSocial SciencesCell AutophagySignaling Pathway	2009	74
The mouse osteopetrotic grey-lethal mutation induces a defect in osteoclast maturation/function Venkatesh Rajapurohitam, Nader Chalhoub, Nadia Benachenhou, Bone Developmental BiologyBone Morphogenic ProteinGeneticsMorphogenesisOsteogenesis	2001	54
Severe Malignant Osteopetrosis Caused by a <i>GL</i> Gene Mutation Paola Quarello, Marco Forni, Laura Barberis, Journal of Bone and Mineral Research	2004	54
Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients’ cohort from Qatar. A population specific founder variant Alice Abdel Aleem, Mahmoud F. Elsaid, Nader Chalhoub, Neuromuscular Disorders Rare DiseasesPatients ’ CohortGenetic DisorderGeneticsGenetic Epidemiology	2020	38
S6k1 is not required for Pten-deficient neuronal hypertrophy Nader Chalhoub, Sara C. Kozma, Suzanne J. Baker Brain Research Pten-deficient Neuronal HypertrophyMolecular PhysiologyMolecular NeuroscienceNeuroscienceMolecular Neurobiology	2006	22
Evaluation of SNP calling using single and multiple-sample calling algorithms by validation against array base genotyping and Mendelian inheritance Pankaj Kumar, Mashael Al‐Shafai, Wadha Ahmed Al Muftah, BMC Research Notes	2014	20

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