Global analysis of lysine acetylation suggests the involvement of protein acetylation in diverse biological processes in rice (Oryza sativa)
Nallamilli, Babi Ramesh Reddy, Edelmann, Mariola J, Zhong, Xiaoxian, Tan, Feng, Mujahid, Hana, Zhang, Jian, Nanduri, Bindu, Peng, Zhaohua
Published in PloS one (20.02.2014)
Published in PloS one (20.02.2014)
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Journal Article
Polycomb group gene OsFIE2 regulates rice (Oryza sativa) seed development and grain filling via a mechanism distinct from Arabidopsis
Nallamilli, Babi Ramesh Reddy, Zhang, Jian, Mujahid, Hana, Malone, Brandon M, Bridges, Susan M, Peng, Zhaohua
Published in PLoS genetics (01.03.2013)
Published in PLoS genetics (01.03.2013)
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Journal Article
Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patients
Nallamilli, Babi Ramesh Reddy, Chakravorty, Samya, Kesari, Akanchha, Tanner, Alice, Ankala, Arunkanth, Schneider, Thomas, da Silva, Cristina, Beadling, Randall, Alexander, John J., Askree, Syed Hussain, Whitt, Zachary, Bean, Lora, Collins, Christin, Khadilkar, Satish, Gaitonde, Pradnya, Dastur, Rashna, Wicklund, Matthew, Mozaffar, Tahseen, Harms, Matthew, Rufibach, Laura, Mittal, Plavi, Hegde, Madhuri
Published in Annals of clinical and translational neurology (01.12.2018)
Published in Annals of clinical and translational neurology (01.12.2018)
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Journal Article
Clinical and Genomic Evaluation of 207 Genetic Myopathies in the Indian Subcontinent
Chakravorty, Samya, Nallamilli, Babi Ramesh Reddy, Khadilkar, Satish Vasant, Singla, Madhu Bala, Bhutada, Ashish, Dastur, Rashna, Gaitonde, Pradnya Satish, Rufibach, Laura E, Gloster, Logan, Hegde, Madhuri
Published in Frontiers in neurology (05.11.2020)
Published in Frontiers in neurology (05.11.2020)
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Journal Article
Clinical utility of RNA sequencing to resolve unusual GNE myopathy with a novel promoter deletion
Chakravorty, Samya, Berger, Kiera, Arafat, Dalia, Nallamilli, Babi Ramesh Reddy, Subramanian, Hari Prasanna, Joseph, Soumya, Anderson, Mary E., Campbell, Kevin P., Glass, Jonathan, Gibson, Greg, Hegde, Madhuri
Published in Muscle & nerve (01.07.2019)
Published in Muscle & nerve (01.07.2019)
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Journal Article
P599: Beyond single nucleotide variants and copy number variations: Spinal muscular atrophy and repeat expansion disorders screening by whole genome sequencing
Liu, Ruby, Reddy Nallamilli, Babi Ramesh, Collins, Christin, Bean, Lora, Hegde, Madhuri
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Journal Article
Reply: Autosomal dominant segregation of CAPN3 c.598_612del15 associated with a mild form of calpainopathy
Nallamilli, Babi Ramesh Reddy, Chakravorty, Samya, Kesari, Akanchha, Bean, Lora, Hegde, Madhuri
Published in Annals of clinical and translational neurology (01.12.2020)
Published in Annals of clinical and translational neurology (01.12.2020)
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Journal Article
P638: Genomic breakpoint analysis facilitates identification of complex rearrangements and re-classification of non-tandem duplications in the DMD gene
Guruju, Naga, Jump, Vanessa, Liu, Ruby, Reddy Nallamilli, Babi Ramesh, Steigerwalt, Jill, Collins, Christin, Bean, Lora, Hegde, Madhuri
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Journal Article
P643: Unveiling noncoding DMD variants: Synergizing RNA sequencing and DNA sequencing for enhanced molecular diagnosis
Pan, Yinghong, Guo, Fen, Ma, Zeqiang, Reddy Nallamilli, Babi Ramesh, Liu, Ruby, Quirin, Kayla, Martin, Ann, Hegde, Madhuri
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Journal Article
P502: How does multiomics help variant reclassification?
Liu, Ruby, Guo, Fen, Reddy Nallamilli, Babi Ramesh, Collins, Christin, Bean, Lora, Guruju, Naga, Hegde, Madhuri
Published in Genetics in Medicine Open (2023)
Published in Genetics in Medicine Open (2023)
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Journal Article
P679: Ultrarapid whole genome sequencing facilitates early definitive diagnosis of rare genetic disorders
Nallamilli, Babi Ramesh Reddy, Lakshmanan, Jagannathan, Ramachander, Vinish, Dhillon, Supan, Liu, Ruby, Pan, Yinghong, Guruju, Naga, Collins, Christin, Bean, Lora, Hegde, Madhuri
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Journal Article
P714: Genome screening of newborns: Sequencing is easy, assessing the clinical utility of genomic findings uncovered in asymptomatic children is challenging
Balciuniene, Jorune, Liu, Ruby, Bean, Lora, Reddy Nallamilli, Babi Ramesh, Guruju, Naga, Chen-Deutsch, Xiangwen, Yousaf, Rizwan, Fura, Kristina, Chin, Eprem, Mathur, Abhinav, Ma, Zeqiang, Carmichael, Jonathan, Collins, Christin, da Silva, Cristina, Kirmse, Brian, Bleyl, Steven, Hegde, Madhuri
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Journal Article
P389: Real-world evidence demonstrating why genome sequencing should be recommended as the first-tier genetic test
Guo, Fen, Liu, Ruby, Pan, Yinghong, Collins, Christin D., Bean, Lora, Reddy Nallamilli, Babi Ramesh, Guruju, Naga, Chen-Deutsch, Xiangwen, Yousaf, Rizwan, Chin, Ephrem, da Silva, Cristina, Mathur, Abhinav, Ma, Zeqiang, Balciuniene, Jorune, Hegde, Madhuri
Published in Genetics in Medicine Open (2023)
Published in Genetics in Medicine Open (2023)
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Journal Article
P425: Unparalleled power of genome sequencing in screening ostensibly healthy newborns and children: Findings from the first real-world dataset
Balciuniene, Jorune, Liu, Ruby, Collins, Christin, Bean, Lora, Guo, Fen, Reddy Nallamilli, Babi Ramesh, Guruju, Naga, Chen-Deutsch, Xiangwen, Yousaf, Rizwan, Fura, Kristina, Chin, Ephrem, da Silva, Cristina, Mathur, Abhinav, Ma, Zeqiang, Hegde, Madhuri
Published in Genetics in Medicine Open (2023)
Published in Genetics in Medicine Open (2023)
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Journal Article
P426: Recognizing the promise and potential pitfalls of genomic medicine through routine rapid whole genome sequencing
Bean, Lora, Collins, Christin, Guo, Fen, Balciuniene, Jorune, Chen-Deutsch, Xiangwen, Reddy Nallamilli, Babi Ramesh, Guruju, Naga, Yousaf, Rizwan, Fura, Kristina, Woodman, Amber, Liu, Ruby, Zhang, Jenny, Liebmann, Kate, Gerow, Julia, Chin, Ephrem, Hegde, Madhuri
Published in Genetics in Medicine Open (2023)
Published in Genetics in Medicine Open (2023)
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Journal Article
Molecular diagnosis of Duchenne muscular dystrophy
Nallamilli, Babi Ramesh Reddy, Ankala, Arunkanth, Hegde, Madhuri
Published in Current protocols in human genetics (01.10.2014)
Published in Current protocols in human genetics (01.10.2014)
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Journal Article
Correction of pseudoexon splicing caused by a novel intronic dysferlin mutation
Dominov, Janice A., Uyan, Özgün, McKenna‐Yasek, Diane, Nallamilli, Babi Ramesh Reddy, Kergourlay, Virginie, Bartoli, Marc, Levy, Nicolas, Hudson, Judith, Evangelista, Teresinha, Lochmuller, Hanns, Krahn, Martin, Rufibach, Laura, Hegde, Madhuri, Brown, Robert H.
Published in Annals of clinical and translational neurology (01.04.2019)
Published in Annals of clinical and translational neurology (01.04.2019)
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Journal Article
Comparative Proteomic Analysis of Cotton Fiber Development and Protein Extraction Method Comparison in Late Stage Fibers
Mujahid, Hana, Pendarvis, Ken, Reddy, Joseph S, Nallamilli, Babi Ramesh Reddy, Reddy, K R, Nanduri, Bindu, Peng, Zhaohua
Published in Proteomes (03.02.2016)
Published in Proteomes (03.02.2016)
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Journal Article
Reply to comment on: A novel dysferlin mutant pseudoexon bypassed with antisense oligonucleotides
Dominov, Janice A., Uyan, Özgün, Sapp, Peter C., McKenna‐Yasek, Diane, Nallamilli, Babi Ramesh Reddy, Hegde, Madhuri, Brown, Robert H.
Published in Annals of clinical and translational neurology (01.07.2015)
Published in Annals of clinical and translational neurology (01.07.2015)
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Journal Article
eP356: Exome sequencing expands the sensitivity and specificity of identification of sequence variants and CNVs in phenotypic females with DSD
Guruju, Naga, Nallamilli, Babi Ramesh Reddy, Jump, Vanessa, Collins, Christin, Hegde, Madhuri
Published in Genetics in medicine (01.03.2022)
Published in Genetics in medicine (01.03.2022)
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Journal Article