| Sequential strategy to identify a susceptibility gene for schizophrenia: Report of potential linkage on chromosome 22q12‐q13. 1: Part 1 AE Pulver, M Karayiorgou, PS Wolyniec, VK Lasseter, L Kasch, G Nestadt, ... American journal of medical genetics 54 (1), 36-43, 1994 | 422 | 1994 |
| LRRK2 Gly2019Ser penetrance in Arab–Berber patients from Tunisia: a case-control genetic study MM Hulihan, L Ishihara-Paul, J Kachergus, L Warren, R Amouri, R Elango, ... The Lancet Neurology 7 (7), 591-594, 2008 | 185 | 2008 |
| Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families L Ishihara, RA Gibson, L Warren, R Amouri, K Lyons, C Wielinski, ... Movement Disorders 22 (1), 55-61, 2007 | 92 | 2007 |
| Genetic mapping of a pulmonary adenoma resistance locus (Par1) in mouse G Manenti, M Gariboldi, R Elango, A Fiorino, LD Gregorio, FS Falvella, ... Nature genetics 12 (4), 455-457, 1996 | 92 | 1996 |
| PINK1 mutations and parkinsonism L Ishihara-Paul, MM Hulihan, J Kachergus, R Upmanyu, L Warren, ... Neurology 71 (12), 896-902, 2008 | 78 | 2008 |
| Induced pluripotent stem cell modelling of HLHS underlines the contribution of dysfunctional NOTCH signalling to impaired cardiogenesis C Yang, Y Xu, M Yu, D Lee, S Alharti, N Hellen, N Ahmad Shaik, ... Human molecular genetics 26 (16), 3031-3045, 2017 | 68 | 2017 |
| Cytogenetic studies in Down syndrome. IC Verma, S Mathew, R Elango, A Shukla Indian pediatrics 28 (9), 991-996, 1991 | 47 | 1991 |
| Multilevel systems biology analysis of lung transcriptomics data identifies key miRNAs and potential miRNA target genes for SARS-CoV-2 infection B Banaganapalli, N Al-Rayes, ZA Awan, FA Alsulaimany, AS Alamri, ... Computers in Biology and Medicine 135, 104570, 2021 | 41 | 2021 |
| A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease L Warren, R Gibson, L Ishihara, R Elango, Z Xue, A Akkari, L Ragone, ... Parkinsonism & related disorders 14 (1), 77-80, 2008 | 40 | 2008 |
| A computational protein phenotype prediction approach to analyze the deleterious mutations of human MED12 gene B Banaganapalli, K Mohammed, IA Khan, JY Al‐Aama, R Elango, ... Journal of cellular biochemistry 117 (9), 2023-2035, 2016 | 35 | 2016 |
| iPSC modeling of severe aplastic anemia reveals impaired differentiation and telomere shortening in blood progenitors D Melguizo-Sanchis, Y Xu, D Taheem, M Yu, K Tilgner, T Barta, ... Cell death & disease 9 (2), 128, 2018 | 34 | 2018 |
| 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 … M Karayiorgou, L Kasch, VK Lasseter, J Hwang, R Elango, DJ Bernardini, ... American journal of medical genetics 54 (4), 345-353, 1994 | 34 | 1994 |
| Divergent genetic and epigenetic post‐zygotic isolation mechanisms in Mus and Peromyscus U Zechner, W Shi, M Hemberger, H Himmelbauer, S Otto, A Orth, ... Journal of Evolutionary Biology 17 (2), 453-460, 2004 | 32 | 2004 |
| Fine mapping of Ath6, a quantitative trait locus for atherosclerosis in mice MK Purcell, JL Mu, DC Higgins, R Elango, H Whitmore, S Harris, B Paigen Mammalian genome 12, 495-500, 2001 | 32 | 2001 |
| In-Silico Analysis of Inflammatory Bowel Disease (IBD) GWAS Loci to Novel Connections M Mesbah-Uddin, R Elango, B Banaganapalli, NA Shaik, FA Al-Abbasi PLoS One 10 (3), e0119420, 2015 | 31 | 2015 |
| Efficient high-resolution genetic mapping of mouse interspersed repetitive sequence PCR products, toward integrated genetic and physical mapping of the mouse genome. L McCarthy, K Hunter, L Schalkwyk, L Riba, S Anson, R Mott, W Newell, ... Proceedings of the National Academy of Sciences 92 (12), 5302-5306, 1995 | 28 | 1995 |
| Dissecting the role of NF-κb protein family and its regulators in rheumatoid arthritis using weighted gene co-expression network JSM Sabir, A El Omri, B Banaganapalli, MA Al-Shaeri, NA Alkenani, ... Frontiers in genetics 10, 1163, 2019 | 25 | 2019 |
| Whole exome sequencing of a consanguineous family identifies the possible modifying effect of a globally rare AK5 allelic variant in celiac disease development … JY Al-Aama, NA Shaik, B Banaganapalli, MA Salama, O Rashidi, ... PloS one 12 (5), e0176664, 2017 | 25 | 2017 |
| Exploring celiac disease candidate pathways by global gene expression profiling and gene network cluster analysis B Banaganapalli, H Mansour, A Mohammed, AM Alharthi, NM Aljuaid, ... Scientific reports 10 (1), 16290, 2020 | 24 | 2020 |
| Molecular modelling and dynamics of CA2 missense mutations causative to carbonic anhydrase 2 deficiency syndrome NA Shaik, HA Bokhari, TA Masoodi, PJ Shetty, GMA Ajabnoor, R Elango, ... Journal of Biomolecular Structure and Dynamics 38 (14), 4067-4080, 2020 | 24 | 2020 |
Noor Ahmad ShaikKing Abdulaziz UniversityVerifierad e-postadress på kau.edu.sa
