RajiP.GrewalMD

PubMed

• Demyelinating Peripheral Neuropathy Caused by the p.R160H Mutation in theGene.
  Leema Reddy Peddareddygari, Raji P Grewal> ;Journal of Community Hospital Internal Medicine Perspectives. 2023 Jan 1
• 8 citations
  Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke.
  Jaworek, T., Xu, H., Gaynor, B., Cole, J., Rannikmae, K., Stanne, T., Tomppo, L., Abedi, V., Amouyel, P., Armstrong, N., Attia, J., Bell, S., Benavente, O., Boncoragli...> ;Neurology. 2022 Oct 17
• 1 citations
  Novel Titin Gene Mutation Causing Autosomal Dominant Limb-Girdle Muscular Dystrophy.
  Leema Reddy Peddareddygari, Kinsi Oberoi, Raji P Grewal> ;Cureus. 2022 Oct 1
• 1 citations
  Clinical and Genetic Analysis of a Patient with CMT4J.
  Leema Reddy Peddareddygari, Raji P Grewal> ;Neurology International. 2022 Feb 10
• 71 citations
  Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies.
  Matthew Traylor, Elodie Persyn, Liisa Tomppo, Sofia Klasson, Vida Abedi, Mark K Bakker, Nuria Torres, Linxin Li, Steven Bell, Loes Rutten-Jacobs, D Tozer, Christoph J....> ;The Lancet. Neurology. 2021 May 1
• 1 citations
  Genotype phenotype analysis in a family carrying truncating mutations in the titin gene.
  Leema Reddy Peddareddygari, Ada Baisre-de Leon, Raji P. Grewal> ;Acta Myologica. 2021 Mar 31
• 2 citations
  Intrafamilial Phenotypic Variability Associated with the I1739V Mutation in the SCN9A Gene.
  Leema Reddy Peddareddygari, Raji P Grewal> ;Case Reports in Neurology. 2021 Feb 25
• 20 citations
  Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations with Stroke
  Keith L. Keene, Hyacinth I. Hyacinth, Joshua C. Bis, Steven J. Kittner, Braxton D. Mitchell, Yu-Ching Cheng, Guillaume Paré, Michael Chong, Martin O'Donnell, James F. ...> ;Stroke. 2020 Jul 22
• 23 citations
  POGLUT1 biallelic mutations cause myopathy with reduced satellite cells, α-dystroglycan hypoglycosylation and a distinctive radiological pattern
  Emilia Servián-Morilla, Macarena Cabrera-Serrano, Katherine Johnson, Ashutosh Pandey, Atsuko Ito, Eloy Rivas, Teodora Chamova, Nuria Muelas, Tiziana Mongini, Shahriar ...> ;Acta Neuropathologica. 2020 Jan 3
• 5 citations
  Genetic Analysis of a Large Family with Migraine, Vertigo, and Motion Sickness.
  Leema Reddy Peddareddygari, Phillip D. Kramer, Philip A. Hanna, Mark A Levenstien, Raji P. Grewal> ;The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 2019 Jul 1
• 8 citations
  Subtype Specificity of Genetic Loci Associated With Stroke in 16 664 Cases and 32 792 Controls.
  Matthew Traylor, Christopher D. Anderson, Loes Rutten-Jacobs, Guido J. Falcone, Mary E. Comeau, Hakan Ay, Cathie Sudlow, Huichun Xu, Braxton D. Mitchell, John W. Cole,...> ;Circulation. Genomic and Precision Medicine. 2019 Jul 1
• 3 citations
  Adult Diagnosis of Type 1 Fiber Predominance Myopathy Caused by Novel Mutations in the RYR1 Gene.
  Leema Reddy Peddareddygari, Kinsi Oberoi, Leroy R. Sharer, Raji P. Grewal> ;Journal of Clinical Neuromuscular Disease. 2019 Jun 1
• 22 citations
  Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting
  Ganesh Chauhan, Adams Hhh., Claudia L. Satizabal, J. C. Bis, A. Teumer, Muralidharan Sargurupremraj, Edith Hofer, S. Trompet, Saima Hilal, Albert V. Smith, Xueqiu Jian...> ;Neurology. 2019 Jan 29
• 7 citations
  Limb Girdle Muscular Dystrophy due to Digenic Inheritance of DES and CAPN3 Mutations.
  Leema Reddy Peddareddygari, Kinsi Oberoi, Raji P. Grewal> ;Case Reports in Neurology. 2018 Sep 18
• 432 citations
  Multi-Ethnic Genome-wide Association Study for Atrial Fibrillation
  Carolina Roselli, Mark Chaffin, Lu-Chen Weng, Stefanie Aeschbacher, Gustav Ahlberg, Christine M. Albert, Peter Almgren, Alvaro Alonso, Christopher D. Anderson, Krishna...> ;Nature Genetics. 2018 Jun 11
• 2 citations
  Novel Mutation in Anoctamin 5 Gene Causing Limb-Girdle Muscular Dystrophy 2L.
  Leema Reddy Peddareddygari, Kinsi Oberoi, Ada Baisre-de Leon, Raji P. Grewal> ;Journal of Clinical Neuromuscular Disease. 2018 Jun 1
• 1 citations
  Clinical and Genetic Analysis of an Asian Indian Family with Charcot-Marie-Tooth Disease Type 4C.
  Raji P. Grewal, Kinsi Oberoi, Leema Reddy Peddareddygari> ;Case Reports in Neurology. 2018 Jan 1
• 3 citations
  Lance-Adams syndrome associated with cerebellar pathology.
  Adam Waddell, Ahmed Dirweesh, Fausto M. Ordonez, Charles Kososky, Leema Reddy Peddareddygari, Raji P. Grewal> ;Journal of Community Hospital Internal Medicine Perspectives. 2017 Jul 13
• 59 citations
  Genetic Variation at 16q24.2 is associated with small vessel stroke
  Matthew Traylor, Rainer Malik, Mike A. Nalls, Ioana Cotlarciuc, Farid Radmanesh, Gudmar Thorleifsson, Ken B. Hanscombe, Carl D. Langefeld, Danish Saleheen, Natalia S. ...> ;Annals of Neurology. 2017 Mar 1
• Positive Germline Selection in Pedigrees With Multiple Endocrine Neoplasia Type 2 Carrying V804M Mutation in the RET Gene.
  Leema Reddy Peddareddygari, Angela Musial Fay, Alexander L. Shifrin, Raji P. Grewal> ;World Journal of Oncology. 2016 Dec 23
• 2 citations
  Role of Therapeutic Plasma Exchange in Treatment of Tumefactive Multiple Sclerosis-Associated Low CD4 and CD8 Levels
  Kristen Lew, Nishith Mewada, Sahana Ramanujam, Bahareh Hassanzadeh, John E. Donahue, Leema Reddy Peddareddygari, Robert Moser, Charles Kososky, Raji P. Grewal> ;Case Reports in Neurology. 2016 Aug 31
• 6 citations
  Focal seizures in a patient with myotonic disorder type 2 co-segregating with a chloride voltage-gated channel 1 gene mutation: a case report.
  Leema Reddy Peddareddygari, Arman Singh Grewal, Raji P. Grewal> ;Journal of Medical Case Reports. 2016 Jun 7
• 2 citations
  Factors Affecting Phenotype Variability in a Family with CMT2B: Gender and LRSAM1 Genotype.
  Leema Reddy Peddareddygari, Kinsi Oberoi, Jaasrini Reddy Vellore, Raji P. Grewal> ;Case Reports in Neurology. 2016 Jun 6
• 100 citations
  Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies
  Ganesh Chauhan, Corey R. Arnold, Audrey Y. Chu, Myriam Fornage, Azadeh Reyahi, Joshua C. Bis, Aki S. Havulinna, Muralidharan Sargurupremraj, Albert V. Smith, Hieab H.H...> ;The Lancet. Neurology. 2016 Jun 1
• Autosomal dominant hereditary spastic paraplegia with axonal sensory motor polyneuropathy maps to chromosome 21q 22.3.
  Leema Reddy Peddareddygari, Philip A. Hanna, Robert P. Igo, Yuqun A. Luo, Sungho Won, Michio Hirano, Raji P. Grewal> ;The International Journal of Neuroscience. 2015 May 22
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