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Ashraf ul Mannan

Observed names: A. Mannan, A. U. Mannan, A.U. Mannan, AU Mannan, Ashraf Mannan, Ashraf U Mannan, Ashraf U. Mannan, Ashraf-ul Mannan, AshrafU Mannan, Mannan, A.U., Mannan, Ashraf, Mannan, Ashraf U., Mannan, Ashraf-ul
Observed institutions: Strand Life Sciences (India), University of Agricultural Sciences, Bangalore, Universitätsmedizin Göttingen, Nanoscale Microscopy and Molecular Physiology of the Brain Cluster of Excellence 171 — DFG Research Center 103, Healthcare Global Enterprises, University of Göttingen, Deutsche Forschungsgemeinschaft
OpenAlex ID: A5112896786
ZFYVE27 (SPG33), a Novel Spastin-Binding Protein, Is Mutated in Hereditary Spastic Paraplegia
2006 · Ashraf U. Mannan, Philip Krawen, et al. · The American Journal of Human Genetics · 144
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Screening of over 1000 Indian patients with breast and/or ovarian cancer with a multi-gene panel: prevalence of BRCA1/2 and non-BRCA mutations
2018 · Jaya Singh, Nishita Thota, et al. · Breast Cancer Research and Treatment · 98
Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia
2008 · Moneef Shoukier, Juergen Neesen, et al. · European Journal of Human Genetics · 94
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Detection of high frequency of mutations in a breast and/or ovarian cancer cohort: implications of embracing a multi-gene panel in molecular diagnosis in India
2016 · Ashraf U Mannan, Jaya Singh, et al. · Journal of Human Genetics · 74
Sall1, Sall2, and Sall4 Are Required for Neural Tube Closure in Mice
2008 · Johann Böhm, Anja Buck, et al. · American Journal Of Pathology · 64
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Spastin, the most commonly mutated protein in hereditary spastic paraplegia interacts with Reticulon 1 an endoplasmic reticulum protein
2006 · Ashraf U. Mannan, Johann Boehm, et al. · Neurogenetics · 57
Functional evaluation of paraplegin mutations by a yeast complementation assay
2010 · Florian Bonn, Krishna Pantakani, et al. · Human Mutation · 49
Mild Overexpression of Mecp2 in Mice Causes a Higher Susceptibility toward Seizures
2013 · Chiranjeevi Bodda, Martesa Tantra, et al. · American Journal Of Pathology · 44
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Mutation in the gene encoding lysosomal acid phosphatase (Acp2) causes cerebellum and skin malformation in mouse
2004 · Ashraf U. Mannan, Elena Roussa, et al. · Neurogenetics · 43
Mutation Spectrum of GNE Myopathy in the Indian Sub-Continent
2018 · Sudha Bhattacharya, Satish V. Khadilkar, et al. · Journal of Neuromuscular Diseases · 41
Multi-gene testing in neurological disorders showed an improved diagnostic yield: data from over 1000 Indian patients
2019 · Aparna Ganapathy, Avshesh Mishra, et al. · Journal of Neurology · 40
Genotype-phenotype correlates of infantile-onset developmental & epileptic encephalopathy syndromes in South India: A single centre experience
2020 · Nandini Mitta, Ramshekhar N Menon, et al. · Epilepsy Research · 38
Purkinje Cell Compartmentation in the Cerebellum of the Lysosomal Acid Phosphatase 2 Mutant Mouse (Nax - Naked-Ataxia Mutant Mouse)
2014 · Karen Bailey, Maryam Rahimi Balaei, et al. · PLoS ONE · 30
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Mild expression differences of MECP2 influencing aggressive social behavior
2014 · Martesa Tantra, Christian Hammer, et al. · EMBO Molecular Medicine · 28
Spastin oligomerizes into a hexamer and the mutant spastin (E442Q) redistribute the wild‐type spastin into filamentous microtubule
2008 · D. V. Krishna Pantakani, Lakshmipuram S. Swapna, et al. · Journal of Neurochemistry · 27
Chronic Mucocutaneous Candidiasis in an Adolescent Boy Due to a Novel Mutation in TRAF3IP2
2019 · Sagar Bhattad, Chitra Dinakar, et al. · Journal of Clinical Immunology · 25
Genetic Counseling, Testing, and Management of HBOC in India: An Expert Consensus Document from Indian Society of Medical and Pediatric Oncology
2020 · Hemant Malhotra, Pradnya Kowtal, et al. · JCO Global Oncology · 24
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Oligomerization of ZFYVE27 (Protrudin) Is Necessary to Promote Neurite Extension
2011 · D. V. Krishna Pantakani, Marta M. Czyzewska, et al. · PLoS ONE · 24
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Next-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort.
2016 · Jaya Singh, Avshesh Mishra, et al. · PubMed Central · 23
Male Mice Lacking the Theg (Testicular Haploid Expressed Gene) Protein Undergo Normal Spermatogenesis and Are Fertile1
2003 · Ashraf U. Mannan, Karim Nayernia, et al. · Biology of Reproduction · 22
Targeted sequencing of the DMD locus
2019 · Sankaramoorthy Aravind, Berty Ashley, et al. · The Indian Journal of Medical Research · 19
MeCP2270 Mutant Protein Is Expressed in Astrocytes as well as in Neurons and Localizes in the Nucleus
2010 · L.A. Kifayathullah, J.P. Arunachalam, et al. · Cytogenetic and Genome Research · 19
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Assessing germline mutational profile and its clinicopathological associations in Triple Negative Breast Cancer
2025 · Jisha John, Ashwini Bapat, et al. · Cancer Genetics · 17
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Lipoprotein Lipase Deficiency
2020 · Shwetha Kuthiroly, Dhanya Yesodharan, et al. · The Indian Journal of Pediatrics · 15
Compound heterozygosity in the SPG4 gene causes hereditary spastic paraplegia
2008 · DVK Pantakani, U Zechner, et al. · Clinical Genetics · 15
Works count: 63
Citation count: 1,182
H-index: 20
I10-index: 29
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