Muhammad Sajid Hussain

Author

Also Known As

Ghulam Rasool, Hussain, Muhammad Sajid, M Sajid Hussain, M. Hussain, M. S. Hussain, M.S. Hussain, Mr. Saddam Hussain, Muhammad S. Hussain, Muhammad Sajid Hussain, Muhammad. S. Hussain

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

University of Cologne National Institute for Biotechnology and Genetic Engineering Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases University Hospital Cologne Pakistan Institute of Engineering and Applied Sciences

About

Muhammad Sajid Hussain is an author at University of Cologne specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	13	999
2	Cell Biology	7	7	748
3	Molecular Genetics	7	7	510
4	Public Health	2	2	67
5	Genetic Medicine	1	1	15

Muhammad Sajid Hussain

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathy Carol-Anne Martin, Ilyas Ahmad, Anna Klingseisen, Nature Genetics Centriole BiogenesisOcular DiseaseDevelopmental BiologyCell RegulationOphthalmology	2014	178
A Truncating Mutation of CEP135 Causes Primary Microcephaly and Disturbed Centrosomal Function Muhammad Sajid Hussain, Shahid Mahmood Baig, Sascha Neumann, The American Journal of Human Genetics Developmental BiologyGenetic DisorderAutophagyPathologyCraniofacial Development	2012	171
Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome Daniela A. Braun, Svjetlana Lovric, David Schapiro, Journal of Clinical Investigation Glomerular DiseaseGeneticsRenal PathologySteroid-resistant Nephrotic SyndromeRenal Inflammation	2018	138
CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephaly Muhammad Sajid Hussain, Shahid Mahmood Baig, Sascha Neumann, Human Molecular Genetics Microtubule OrganizationCytogeneticsGeneticsPathologyMolecular Genetics	2013	120
Seeing clearly: the dominant and recessive nature of<i>FOXE3</i>in eye developmental anomalies Robert J. Osborne, Martin Farrall, Alexander W. Wyatt, Human Mutation Eye AnomaliesDevelopmental AnomalyOcular DiseaseDevelopmental BiologyOphthalmology	2009	88
Mutations of <i>KIF14</i> cause primary microcephaly by impairing cytokinesis Abubakar Moawia, Ranad Shaheen, Sajida Rasool, Annals of Neurology	2017	83
A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family Muzammil Ahmad Khan, Verena Rupp, Meritxell Orpinell, Human Molecular Genetics CytogeneticsGeneticsPathologyMolecular GeneticsCell Cycle	2014	68
RRP7A links primary microcephaly to dysfunction of ribosome biogenesis, resorption of primary cilia, and neurogenesis Muhammad Farooq, Louise Lindbæk, Nicolai Krogh, Nature Communications	2020	56
Genetic heterogeneity in Pakistani microcephaly families Muhammad Sajid Hussain, Syeda Marriam Bakhtiar, Muhammad Farooq, Clinical Genetics Mcph FamiliesMendelian DisorderGenetic DisorderMedicineGenetics	2012	52
Preaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis-regulatory element ZRS Muhammad Farooq, Jesper T. Troelsen, Mette Boyd, European Journal of Human Genetics Developmental BiologyGeneticsGenomic MechanismGene RegulationGene Structure	2010	49

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