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B. Nallamilli · SciRah

Researcher profile · Semantic Scholar

B. Nallamilli

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B. Nallamilli — researcher profile on SciRah

h-index: 19
Works: 46
Citations: 1,134

Most-cited papers

Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patients
B. Nallamilli, Samya Chakravorty, A. Kesari, Alice K. Tanner +18 more
2018Annals of Clinical and Translational Neurology166 citations Open access
Semantic Scholar
Global Analysis of Lysine Acetylation Suggests the Involvement of Protein Acetylation in Diverse Biological Processes in Rice (Oryza sativa)
B. Nallamilli, Mariola J. Edelmann, Xiao-Xia Zhong, F. Tan +4 more
2014PLoS ONE109 citations Open access
Semantic Scholar
Polycomb Group Gene OsFIE2 Regulates Rice (Oryza sativa) Seed Development and Grain Filling via a Mechanism Distinct from Arabidopsis
B. Nallamilli, Jian Zhang, Hana Mujahid, Brandon M. Malone +2 more
2013PLoS Genetics103 citations Open access
Semantic Scholar
OsMADS6 plays an essential role in endosperm nutrient accumulation and is subject to epigenetic regulation in rice (Oryza sativa).
Jian Zhang, B. Nallamilli, Hana Mujahid, Zhao-Hua Peng
2010The Plant Journal93 citations Open access
Semantic Scholar
Plant Long ncRNAs: A New Frontier for Gene Regulatory Control
Jian Zhang, Hana Mujahid, Yuxuan Hou, B. Nallamilli +1 more
201358 citations Open access
Semantic Scholar
A comprehensive quantitative phosphoproteome analysis of rice in response to bacterial blight
Yuxuan Hou, Jiehua Qiu, Xiao-Hong Tong, Xiangjin Wei +4 more
2015BMC Plant Biology52 citations Open access
Semantic Scholar
Low Pass-Genome Sequencing: Validation and diagnostic utility from 409 clinical cases of low-pass genome sequencing for the detection of copy number variants (CNVs) to replace constitutional microarray.
A. Chaubey, S. Shenoy, A. Mathur, Zeqiang Ma +6 more
2020Journal of Molecular Diagnostics50 citations Open access
Semantic Scholar
Removal of high‐abundance proteins for nuclear subproteome studies in rice (Oryza sativa) endosperm
Guosheng Li, B. Nallamilli, F. Tan, Zhao-Hua Peng
2008Electrophoresis47 citations
Semantic Scholar
Clinical and Genomic Evaluation of 207 Genetic Myopathies in the Indian Subcontinent
Samya Chakravorty, B. Nallamilli, S. Khadilkar, M. Singla +6 more
2020Frontiers in Neurology45 citations Open access
Semantic Scholar
A single NGS‐based assay covering the entire genomic sequence of the DMD gene facilitates diagnostic and newborn screening confirmatory testing
B. Nallamilli, A. Chaubey, C. Valencia, L. Stansberry +10 more
2021Human Mutation44 citations Open access
Semantic Scholar
Quantitative phosphoproteomic analysis of early seed development in rice (Oryza sativa L.)
Jiehua Qiu, Yuxuan Hou, Xiao-Hong Tong, Yi-Feng Wang +6 more
2015Plant Molecular Biology41 citations
Semantic Scholar
Molecular Diagnosis of Duchenne Muscular Dystrophy
B. Nallamilli, Arunkanth Ankala, M. Hegde
2014Current Protocols in Human Genetics37 citations
Semantic Scholar
Evidence from 2100 index cases supports genome sequencing as a first-tier genetic test.
Fen Guo, Ruby Liu, Ying-Hong Pan, Christin D. Collins +11 more
2023Genetics in Medicine29 citations Open access
Semantic Scholar
A novel dysferlin mutant pseudoexon bypassed with antisense oligonucleotides
J. Dominov, Özgün Uyan, P. Sapp, D. McKenna-Yasek +3 more
2014Annals of Clinical and Translational Neurology25 citations Open access
Semantic Scholar
Correction of pseudoexon splicing caused by a novel intronic dysferlin mutation
J. Dominov, Özgün Uyan, D. McKenna-Yasek, B. Nallamilli +10 more
2019Annals of Clinical and Translational Neurology23 citations Open access
Semantic Scholar
Detecting APC Gene Mutations in Familial Adenomatous Polyposis (FAP)
B. Nallamilli, M. Hegde
2017Current Protocols in Human Genetics22 citations
Semantic Scholar
Nuclear proteome response to cell wall removal in rice (Oryza sativa)
Hana Mujahid, F. Tan, Jian Zhang, B. Nallamilli +2 more
2013Proteome Science22 citations Open access
Semantic Scholar
CLINICAL UTILITY OF RNA SEQUENCING TO RESOLVE UNUSUAL GNE MYOPATHY WITH A NOVEL PROMOTER DELETION
Samya Chakravorty, K. Berger, D. Arafat, B. Nallamilli +7 more
2019Muscle and Nerve21 citations Open access
Semantic Scholar
Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy in Patients Clinically Suspected of FSHD Using Optical Genome Mapping
Naga M. Guruju, Vanessa Jump, R. Lemmers, S. M. van der Maarel +8 more
2023Neurology: Genetics20 citations Open access
Semantic Scholar
Diagnostic overview of blood‐based dysferlin protein assay for dysferlinopathies
Arunkanth Ankala, B. Nallamilli, L. Rufibach, Esther Hwang +1 more
2014Muscle and Nerve19 citations
Semantic Scholar
At-Risk Genomic Findings for Pediatric-Onset Disorders From Genome Sequencing vs Medically Actionable Gene Panel in Proactive Screening of Newborns and Children
J. Balciuniene, Ruby Liu, Lora J. H. Bean, Fen Guo +12 more
2023JAMA Network Open18 citations Open access
Semantic Scholar
A report on GNE myopathy: Individuals of Rajasthan ancestry share the Roma gene.
S. Khadilkar, B. Nallamilli, Ashish G. Bhutada, M. Hegde +3 more
2017Journal of Neurological Sciences16 citations
Semantic Scholar
Comparative Proteomic Analysis of Cotton Fiber Development and Protein Extraction Method Comparison in Late Stage Fibers
Hana Mujahid, K. Pendarvis, J. Reddy, B. Nallamilli +3 more
2016Proteomes15 citations Open access
Semantic Scholar
Genetic Testing for Hereditary Nonpolyposis Colorectal Cancer (HNPCC)
B. Nallamilli, M. Hegde
2009Current Protocols in Human Genetics12 citations
Semantic Scholar
Detection of Dysferlin Gene Pathogenic Variants in the Indian Population in Patients Predicted to have a Dysferlinopathy Using a Blood-based Monocyte Assay and Clinical Algorithm: A Model for Accurate and Cost-effective Diagnosis
Rashna S. Dastur, P. Gaitonde, Munira Kachwala, B. Nallamilli +8 more
2017Annals of Indian Academy of Neurology11 citations Open access
Semantic Scholar
Pompe disease ascertained through The Lantern Project, 2018-2021: Next-generation sequencing and enzymatic testing to overcome obstacles to diagnosis.
Lisa Sniderman King, Ying-Hong Pan, B. Nallamilli, Madhuri R. Hegde +5 more
2023Molecular Genetics and Metabolism10 citations Open access
Semantic Scholar
Molecular Diagnosis of Duchenne Muscular Dystrophy Using Single NGS‐Based Assay
B. Nallamilli, Naga M. Guruju, Vanessa Jump, Ruby Liu +1 more
2023Current Protocols7 citations
Semantic Scholar
Combined sequence and copy number analysis improves diagnosis of limb girdle and other myopathies
B. Nallamilli, Ying-Hong Pan, Lisa Sniderman King, L. Jagannathan +5 more
2023Annals of Clinical and Translational Neurology6 citations Open access
Semantic Scholar
Limb girdle weakness responding to salbutamol: An Indian family with DOK7 mutation
S. Khadilkar, Ashish G. Bhutada, B. Nallamilli, Madhuri R. Hegde
2015Indian Pediatrics6 citations
Semantic Scholar
Enhancing Fabry disease screening and diagnostic efficiency: Integration of enzyme, biomarker, and next-generation sequencing testing.
Ying-Hong Pan, Lisa Sniderman King, Elizabeth Vengoechea, Ruby Liu +11 more
2025Molecular Genetics and Metabolism4 citations
Semantic Scholar
Focused Exome Sequencing Gives a High Diagnostic Yield in The Indian Sub-Continent.
A. Duraisamy, Ruby Liu, Shruti Sureshkumar, Rajiv Rose +20 more
2024Journal of Molecular Diagnostics2 citations
Semantic Scholar
Unveiling non-coding DMD variants: synergising RNA sequencing and DNA sequencing for enhanced molecular diagnosis
Ying-Hong Pan, B. Nallamilli, Ruby Liu, Naga M. Guruju +8 more
2024Journal of Medical Genetics2 citations
Semantic Scholar
Genetic basis of oculopharyngeal muscular dystrophy: detection of alanine repeats in PABPN1 gene by next generation sequencing
B. Nallamilli, A. McCarty, A. Kesari, Yang Wang +6 more
20211 citations
Semantic Scholar
Reply: Autosomal dominant segregation of CAPN3 c.598_612del15 associated with a mild form of calpainopathy
B. Nallamilli, Samya Chakravorty, A. Kesari, Lora Bean +1 more
2020Annals of Clinical and Translational Neurology1 citations Open access
Semantic Scholar
A comprehensive quantitative phosphoproteome analysis of rice in response to bacterial blight
Yuxuan Hou, Jiehua Qiu, Xiao-Hong Tong, Xiangjin Wei +4 more
2015BMC Plant Biology1 citations Open access
Semantic Scholar
Nuclear proteome response to cell wall removal in rice (Oryza sativa)
Hana Mujahid, F. Tan, Jian Zhang, B. Nallamilli +2 more
2013Proteome Science1 citations Open access
Semantic Scholar
High Diagnosis Rate for Nonimmune Hydrops Fetalis With Prenatal Clinical Genome: Expanded Results From the Hydrops-Yielding Diagnostic Results of Prenatal Sequencing (HYDROPS) Study.
S. Rice, Mona M. Makhamreh, S. Wodoslawsky, Mariella Toro +7 more
2026American Journal of Medical Genetics. Part A0 citations Open access
Semantic Scholar
P679: Ultrarapid whole genome sequencing facilitates early definitive diagnosis of rare genetic disorders
B. Nallamilli, Jagannathan Lakshmanan, Vinish Ramachander, Supan Dhillon +6 more
2024Genetics in Medicine Open0 citations Open access
Semantic Scholar
P476: Identification and accurate sizing of D4Z4 repeat units in patients suspected of facioscapulohumeral muscular dystrophy (FSHD) using optical genome mapping*
Naga M. Guruju, Vanessa Jump, B. Nallamilli, Ruby Liu +2 more
2023Genetics in Medicine Open0 citations Open access
Semantic Scholar
P518: Limb-girdle muscular dystrophy and other myopathy patients diagnostic yield in large cohort of more than 6000 patients*
B. Nallamilli, Ying-Hong Pan, Jagannathan Lakshmanan, Vinish Ramachander +1 more
2023Genetics in Medicine Open0 citations Open access
Semantic Scholar
P519: Evidence of complex inheritance patterns in limb-girdle and other muscular dystrophies: Synergistic heterozygosity and multigenic inheritance
Madhuri R. Hegde, B. Nallamilli, Ying-Hong Pan, Jagannathan Lakshmanan +2 more
2023Genetics in Medicine Open0 citations Open access
Semantic Scholar
eP356: Exome sequencing expands the sensitivity and specificity of identification of sequence variants and CNVs in phenotypic females with DSD
Naga M. Guruju, B. Nallamilli, Vanessa Jump, Christin D. Collins +1 more
2022Genetics in Medicine0 citations Open access
Semantic Scholar
eP380: Sequencing of entire 2.2 MB DMD gene facilitates diagnostic testing and aids selection of patients for therapeutic intervention
B. Nallamilli, Naga M. Guruju, L. Jagannathan, Vinish Ramachander +2 more
2022Genetics in Medicine0 citations Open access
Semantic Scholar
Polycomb Gene Regulation in Rice Endosperm Development and Global Analysis of Protein Acetylation in Rice
B. Nallamilli
20200 citations
Semantic Scholar
Reply to comment on: A novel dysferlin mutant pseudoexon bypassed with antisense oligonucleotides
J. Dominov, Özgün Uyan, P. Sapp, D. McKenna-Yasek +3 more
2015Annals of Clinical and Translational Neurology0 citations Open access
Semantic Scholar
Breakpoint spanning PCR of the DMD gene to resolve discrepancy between MLPA and targeted aCGH results to confirm predicted effect on reading frame
E. Ulm, M. Hegde, B. Nallamilli, J. Alexander +1 more
20150 citations
Semantic Scholar

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