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K

Kiran Polavarapu

Children's Hospital of Eastern Ontario
H指数:22
被引数:1,447

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Systematic reanalysis of next-generation sequencing data in 101 neuromuscular disorder families enhances diagnostic yield, reveals intronic variants, and identifies a novel disease gene

对101个神经肌肉疾病家系下一代测序数据的系统性再分析提高了诊断率，揭示了内含子变异，并鉴定出一个新的疾病基因

Journal of Neurology
IF4.6
2026-07-200
PRE
Sivasankar Malaichamy; Kiran Polavarapu; Rachel Thompson; Romane Idoux; Sally Spendiff; Veronika Karcagi; Agnes Herczegfalvi; Momen Almomen; Rosana Herminia Scola; Paulo José Lorenzoni; Edmar Zanoteli; Antonio Alberto Zambon; Clara Gontijo Camelo; Eduardo de Paula Estephan; Thenral S. Geetha; Vedam L. Ramprasad; Seena Vengalil; Saraswati Nashi; Muddassu Keerthipriya; Dipti Baskar; Veeramani Preethish-Kumar; Ananthapadmanabha Kotambail; David Muhmann; Ulrike Schara-Schmidt; Steven Laurie; Leslie Matalonga; Sergi Beltran; Andreas Roos; Ivo Barić; Atchayaram Nalini; Hanns Lochmüller
Unveiling MYH2-related myopathy: Histological-genetic insights from a case series and systematic review

揭示MYH2相关肌病：来自病例系列和系统综述的组织学-遗传学见解

Journal of Neuromuscular Diseases
IF3.4
2025-11-180
OA
Beatrice Labella; Guy Brochier; Maud Beuvin; Emmanuelle Lacene; Anais Chanut; Angeline Madelaine; Clemence Labasse; Aurelie Méneret; Andreas Roos; Heike Kölbel; Adrian Levine; Grace Yoon; Juliette Svahn; Francoise Bouhour; Natalie Streichenberger; Aleksandra Nadaj-Pakleza; Edoardo Malfatti; Guillaume Bassez; Anthony Behin; Pascal Laforet; Rocio Nur Villar-Quiles; Sarah Leonard-Louis; Thierry Maisonobe; Tanya Stojkovic; Bruno Eymard; Norma Beatriz Romero; Alessandro Padovani; Massimiliano Filosto; Denise Cassandrini; Valerie Biancalana; John Rendu; Kiran Polavarapu; Corinne Métay; Teresinha Evangelista
Acute-onset axonal neuropathy following infection in children with biallelic RCC1 variants: a case series

儿童中biallelic RCC1变异者在感染后出现的急性起病轴索神经病：一个病例系列

lancet neurology
IF0
2025-07-160
OAAI
J Robert Harkness; John H McDermott; Shea Marsden; Peter Jamieson; Kay A Metcalfe; Naz Khan; William L Macken; Robert D S Pitceathly; Christopher J Record; Reza Maroofian; Kleopas Kleopa; Kyproula Christodoulou; Ataf Sabir; Lily Islam; Saikat Santra; Enise Avci Durmusalioglu; Tahir Atik; Esra Isik; Ozgur Cogulu; Jill E Urquhart; Glenda M Beaman; Leigh A Demain; Adam Jackson; Alexander J M Blakes; Helen J Byers; Hayley Bennett; Wei-Hsiang Lin; Antony Adamson; Sanjai Patel; Wyatt W Yue; Robert W Taylor; Janine Reunert; Thorsten Marquardt; Rebecca Buchert; Tobias Haack; Heike Losch; Lukas Ryba; Petra Lassuthova; Radka Valkovičová; Jana Haberlová; Barbora Lauerová; Eva Trúsiková; Kiran Polavarapu; Ozge Aksel Kilicarslan; Hanns Lochmüller; Mina Zamani; Niloofar Chamanrou; Gholamreza Shariati; Saeid Sadeghian; Reza Azizimalamiri; Sateesh Maddirevula; Muhammad AlMuhaizea; Fowzan S Alkuraya; Rita Horvath; Serdal Gungor; Adnan Manzur; Pinki Munot; Rachael Matthews; Siddharth Banka; Mary M Reilly; Daimark Bennett; Raymond T O’Keefe; William G Newman
Dominant rhabdomyolysis linked to a recurrent ATP2A2 variant reducing SERCA2 function in muscle

显性肌溶解症与复发ATP2A2变异相关，该变异降低了肌肉中SERCA2的功能

BRAIN
IF11.7
2025-05-010
OAAI
Malaichamy, Sivasankar; Idoux, Romane; Polavarapu, Kiran; Sikic, Katarina; Holla, Elisa; Thompson, Rachel; Spendiff, Sally; Schaenzer, Anne; Kuesters, Benno; Freeman, Emily; Hentschel, Andreas; O'Neil, Daniel; Carmona-Martinez, Ricardo; Dobelmann, Vera; Tucht, Calvin; Schouten, Meyke; Ruck, Tobias; Schara-Schmidt, Ulrike; Kamsteeg, Erik-Jan; Ramadza, Danijela Petkovic; Jakovcevic, Antonia; Zigman, Tamara; Cavka, Mislav; Karcagi, Veronika; Herczegfalvi, Agnes; Laurie, Steven; Matalonga, Leslie; Beltran, Sergi; Horvath, Rita; Voermans, Nicol; Roos, Andreas; Baric, Ivo; Lochmueller, Hanns
Phenotype-driven genomics enhance diagnosis in children with unresolved neuromuscular diseases (27 Sept, 10.1038/s41431-024-01699-4, 2024)
EUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
2024-12-100
PRE
Estevez-Arias, Berta; Matalonga, Leslie; Yubero, Delia; Polavarapu, Kiran; Codina, Anna; Ortez, Carlos; Carrera-Garcia, Laura; Exposito-Escudero, Jesica; Jou, Cristina; Meyer, Stefanie; Kilicarslan, Ozge Aksel; Aleman, Alberto; Thompson, Rachel; Luknarova, Rebeka; Esteve-Codina, Anna; Gut, Marta; Laurie, Steven; Demidov, German; Yepez, Vicente A.; Beltran, Sergi; Gagneur, Julien; Topf, Ana; Lochmueller, Hanns; Nascimento, Andres; Hoenicka, Janet; Palau, Francesc; Benito, Daniel Natera-de
Diagnosing missed cases of spinal muscular atrophy in genome, exome, and panel sequencing data sets

在基因组、外显子组和基因 panel 测序数据集中诊断脊髓性肌萎缩症漏诊病例

GENETICS IN MEDICINE
IF6.2
2024-12-011
PRE
Weisburd, Ben; Sharma, Rakshya; Pata, Villem; Reimand, Tiia; Ganesh, Vijay S.; Austin-Tse, Christina; Osei-Owusu, Ikeoluwa; O'Heir, Emily; O'Leary, Melanie; Pais, Lynn; Stafki, Seth A.; Daugherty, Audrey L.; Folland, Chiara; Peric, Stojan; Fahmy, Nagia; Udd, Bjarne; Horakova, Magda; Lusakowska, Anna; Manoj, Rajanna; Nalini, Atchayaram; Karcagi, Veronika; Polavarapu, Kiran; Lochmuller, Hanns; Horvath, Rita; Bonnemann, Carsten G.; Donkervoort, Sandra; Haliloglu, Goknur; Herguner, Ozlem; Kang, Peter B.; Scott, Hamish S.; Topf, Ana; Straub, Volker; Pajusalu, Sander; Ounap, Katrin; Tiao, Grace; Rehm, Heidi L.; O'Donnell-Luria, Anne
Current insights in ultra-rare adenylosuccinate synthetase 1 myopathy - meeting report on the First Clinical and Scientific Conference. 3 June 2024, National Centre for Advancing Translational Science, Rockville, Maryland, the United States of America
ORPHANET JOURNAL OF RARE DISEASES
IF3.5
2024-11-261
OAAI
Rybalka, Emma; Park, Hyung Jun; Nalini, Atchayaram; Baskar, Dipti; Polavarapu, Kiran; Durmus, Hacer; Xia, Yang; Wan, Linlin; Shieh, Perry B.; Moghadaszadeh, Behzad; Beggs, Alan H.; Mack, David L.; Smith, Alec S. T.; Hanna-Rose, Wendy; Jinnah, Hyder A.; Timpani, Cara A.; Shen, Min; Upadhyay, Jaymin; Brault, Jeffrey J.; Hall, Matthew D.; Baweja, Naveen; Kakkar, Priyanka
MICU1 related myopathy - a rare report from India

MICU1相关肌病——来自印度的罕见病例报告

JOURNAL OF NEUROMUSCULAR DISEASES
IF3.4
2024-10-290
OA
Baskar, Dipti; Ganji, Suma Reddy; Thomas, Aneesha; Polavarapu, Kiran; Nandeesh, Bevinahalli N.; Sanka, Sai Bhargava; Srivastava, Kosha; Kotambail, Ananthapadmanabha; Arunachal, Gautham; Boddu, Vijay Kumar; Nashi, Saraswati; Nalini, Atchayaram
Phenotype-driven genomics enhance diagnosis in children with unresolved neuromuscular diseases
EUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
2024-09-272
PRE
Estevez-Arias, Berta; Matalonga, Leslie; Yubero, Delia; Polavarapu, Kiran; Codina, Anna; Ortez, Carlos; Carrera-Garcia, Laura; Exposito-Escudero, Jesica; Jou, Cristina; Meyer, Stefanie; Kilicarslan, Ozge Aksel; Aleman, Alberto; Thompson, Rachel; Luknarova, Rebeka; Esteve-Codina, Anna; Gut, Marta; Laurie, Steven; Demidov, German; Yepez, Vicente A.; Beltran, Sergi; Gagneur, Julien; Topf, Ana; Lochmueller, Hanns; Nascimento, Andres; Hoenicka, Janet; Palau, Francesc; Natera-de Benito, Daniel
Advancing the Understanding of Vesicle-Associated Membrane Protein 1-Related Congenital Myasthenic Syndrome: Phenotypic Insights, Favorable Response to 3,4-Diaminopyridine, and Clinical Characterization of Five New Cases
PEDIATRIC NEUROLOGY
IF2.1
2024-08-010
PRE
Natera-deBenito, Daniel; Pugliese, Alessia; Polavarapu, Kiran; Guergueltcheva, Velina; Tournev, Ivailo; Todorova, Albena; Ribeiro, Joana Afonso; Fernandez-Mayoralas, Daniel M.; Ortez, Carlos; Martorell, Loreto; Estevez-Arias, Berta; Matalonga, Leslie; Laurie, Steven; Jou, Cristina; Lau, Jarred; Thompson, Rachel; Shen, Xinming; Engel, Andrew G.; Nascimento, Andres; Lochmuller, Hanns; Selcen, Duygu
Phenotype-Genotype Correlation of a Cohort of Patients with Congenital Myopathy: A Single Centre Experience from India
JOURNAL OF NEUROMUSCULAR DISEASES
IF3.4
2024-06-292
OAAI
Harikrishna, Ganaraja Valakunja; Padmanabha, Hansashree; Polavarapu, Kiran; Anjanappa, Ram Murthy; Preethish-Kumar, Veeramani; Nandeesh, Bevinahalli Nanjegowda; Vengalil, Seena; Nashi, Saraswati; Baskar, Dipti; Thomas, Aneesha; Bardhan, Mainak; Arunachal, Gautham; Menon, Deepak; Sanka, Sai Bhargava; Manjunath, Nisha; Nalini, Atchayaram

研究方向

暂未获取到该数据
A
Atchayaram Nalini
H 指数:35论文数:419被引数:4,790
S
Seena Vengalil
H 指数:20论文数:205被引数:1,433
S
Saraswati Nashi
H 指数:17论文数:164被引数:848
M
Mainak Bardhan
H 指数:38论文数:198被引数:2.8万
V
Veeramani Preethish‐Kumar
H 指数:21论文数:112被引数:1,184
G
Gautham Arunachal
H 指数:10论文数:113被引数:405
H
Hanns Lochmüller
H 指数:100论文数:1,567被引数:3.8万
D
Dipti Baskar
H 指数:6论文数:75被引数:145
A
Akshata Huddar
H 指数:7论文数:46被引数:159
V
Veeramani Preethish Kumar
H 指数:3论文数:30被引数:58