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Ramu Elango
Observed names:
E Ramu,
Elango Ramu,
Elango, R,
Elango, R.,
Elango, Ramu,
R Elango,
R. Elango,
Ramu ELANGO
show all 8
Institution:
King Abdulaziz University
Observed institutions:
Mayo Clinic,
Johns Hopkins University,
King Abdulaziz University,
GlaxoSmithKline (United Kingdom),
GlaxoSmithKline Research & Development Limited (United Kingdom),
All India Institute of Medical Sciences,
Massachusetts Institute of Technology
show all 7
ORCID:
0000-0003-4264-2135
Observed ORCID:
0000-0003-4264-2135
OpenAlex ID:
A5049268048
Sequential strategy to identify a susceptibility gene for schizophrenia: Report of potential linkage on chromosome 22q12‐q13.1: Part 1
1994
·
Ann E. Pulver
, Maria Karayiorgou
, et al.
·
American Journal of Medical Genetics
·
380
PDF
LRRK2 Gly2019Ser penetrance in Arab–Berber patients from Tunisia: a case-control genetic study
2008
·
Mary M Hulihan
, Lianna Ishihara-Paul
, et al.
·
The Lancet Neurology
·
191
Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families
2006
·
Lianna Ishihara
, Rachel A. Gibson
, et al.
·
Movement Disorders
·
93
Induced pluripotent stem cell modelling of HLHS underlines the contribution of dysfunctional NOTCH signalling to impaired cardiogenesis
2017
·
Chunbo Yang
, Yaobo Xu
, et al.
·
Human Molecular Genetics
·
67
PDF
Genetic mapping of a pulmonary adenoma resistance locus (Par1) in mouse
1996
·
Giacomo Manenti
, Manuela Gariboldi
, et al.
·
Nature Genetics
·
66
PINK1 mutations and parkinsonism
2008
·
L. Ishihara-Paul
, M. M. Hulihan
, et al.
·
Neurology
·
64
PDF
Multilevel systems biology analysis of lung transcriptomics data identifies key miRNAs and potential miRNA target genes for SARS-CoV-2 infection
2021
·
Babajan Banaganapalli
, Nuha Al-Rayes
, et al.
·
Computers in Biology and Medicine
·
44
A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease
2007
·
L. Warren
, R. Gibson
, et al.
·
Parkinsonism & Related Disorders
·
42
Paget’s disease: a review of the epidemiology, etiology, genetics, and treatment
2023
·
Babajan Banaganapalli
, Ibrahim Fallatah
, et al.
·
Frontiers in Genetics
·
41
PDF
iPSC modeling of severe aplastic anemia reveals impaired differentiation and telomere shortening in blood progenitors
2018
·
Dario Melguizo-Sanchis
, Yaobo Xu
, et al.
·
Cell Death and Disease
·
36
PDF
Nationwide survey on awareness of consanguinity and genetic diseases in Saudi Arabia: challenges and potential solutions to reduce the national healthcare burden
2024
·
Nura A. Yousef
, Ashraf A. ElHarouni
, et al.
·
Human Genomics
·
34
PDF
Identification of key regulatory genes connected to NF-κB family of proteins in visceral adipose tissues using gene expression and weighted protein interaction network
2019
·
Jamal S. M. Sabir
, Abdelfatteh El Omri
, et al.
·
PLoS ONE
·
29
PDF
In-Silico Analysis of Inflammatory Bowel Disease (IBD) GWAS Loci to Novel Connections
2015
·
Md. Mesbah-Uddin
, Ramu Elango
, et al.
·
PLoS ONE
·
29
PDF
Exploring celiac disease candidate pathways by global gene expression profiling and gene network cluster analysis
2020
·
Babajan Banaganapalli
, Haifa Mansour
, et al.
·
Scientific Reports
·
28
PDF
Divergent genetic and epigenetic post-zygotic isolation mechanisms in Mus and Peromyscus
2004
·
U. Zechner
, W. Shi
, et al.
·
Journal of Evolutionary Biology
·
28
Efficient high-resolution genetic mapping of mouse interspersed repetitive sequence PCR products, toward integrated genetic and physical mapping of the mouse genome.
1995
·
L McCarthy
, K Hunter
, et al.
·
Proceedings of the National Academy of Sciences
·
28
Cytogenetic studies in Down syndrome.
1991
·
I C Verma
, S Mathew
, et al.
·
PubMed
·
28
A Computational Protein Phenotype Prediction Approach to Analyze the Deleterious Mutations of Human MED12 Gene
2016
·
Babajan Banaganapalli
, Kaleemuddin Mohammed
, et al.
·
Journal of Cellular Biochemistry
·
27
Dissecting the Role of NF-κb Protein Family and Its Regulators in Rheumatoid Arthritis Using Weighted Gene Co-Expression Network
2019
·
Jamal S. M. Sabir
, Abdelfatteh El Omri
, et al.
·
Frontiers in Genetics
·
26
PDF
Report from the Maryland epidemiology schizophrenia linkage study: No evidence for linkage between schizophrenia and a number of candidate and other genomic regions using a complex dominant model
1994
·
Maria Karayiorgou
, Laura Kasch
, et al.
·
American Journal of Medical Genetics
·
26
Molecular modelling and dynamics of CA2 missense mutations causative to carbonic anhydrase 2 deficiency syndrome
2019
·
Noor A. Shaik
, Hifaa A. Bokhari
, et al.
·
Journal of Biomolecular Structure and Dynamics
·
25
Fine mapping of Ath6, a quantitative trait locus for atherosclerosis in mice
2001
·
Maureen K. Purcell
, Jian-Long Mu
, et al.
·
Mammalian Genome
·
25
Expanded Somatic Mutation Spectrum of MED12 Gene in Uterine Leiomyomas of Saudi Arabian Women
2018
·
Ghada M. A. Ajabnoor
, Nesma Amin Mohammed
, et al.
·
Frontiers in Genetics
·
24
PDF
Myocardial infarction biomarker discovery with integrated gene expression, pathways and biological networks analysis
2020
·
Abdulrahman Mujalli
, Babajan Banaganapalli
, et al.
·
Genomics
·
21
PDF
Integrative system biology and mathematical modeling of genetic networks identifies shared biomarkers for obesity and diabetes
2022
·
Abdulhadi Ibrahim H. Bima
, Ayman Zaky Elsamanoudy
, et al.
·
Mathematical Biosciences & Engineering
·
20
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Works count:
105
Citation count:
1,955
H-index:
23
I10-index:
55
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