Author Correction: Novel genetic association of the Furin gene polymorphism rs1981458 with COVID-19 severity among Indian populations
Pandey, Rudra Kumar, Srivastava, Anshika, Mishra, Rahul Kumar, Singh, Prajjval Pratap, Chaubey, Gyaneshwer
Published in Scientific reports (25.04.2024)
Published in Scientific reports (25.04.2024)
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Journal Article
Atomistic nonlinear carrier dynamics in Ge
Srivastava, Anshika, Srivastava, Pankaj, Srivastava, Anchal, Saxena, P K
Published in Scientific reports (06.04.2023)
Published in Scientific reports (06.04.2023)
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Journal Article
Homozygous p.(Glu87Lys) variant in ISCA1 is associated with a multiple mitochondrial dysfunctions syndrome
Shukla, Anju, Hebbar, Malavika, Srivastava, Anshika, Kadavigere, Rajagopal, Upadhyai, Priyanka, Kanthi, Anil, Brandau, Oliver, Bielas, Stephanie, Girisha, Katta M
Published in Journal of human genetics (01.07.2017)
Published in Journal of human genetics (01.07.2017)
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Journal Article
Genetic Association of ACE2 rs2285666 Polymorphism With COVID-19 Spatial Distribution in India
Srivastava, Anshika, Bandopadhyay, Audditiya, Das, Debashurti, Pandey, Rudra Kumar, Singh, Vanya, Khanam, Nargis, Srivastava, Nikhil, Singh, Prajjval Pratap, Dubey, Pavan Kumar, Pathak, Abhishek, Gupta, Pranav, Rai, Niraj, Sultana, Gazi Nurun Nahar, Chaubey, Gyaneshwer
Published in Frontiers in genetics (25.09.2020)
Published in Frontiers in genetics (25.09.2020)
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Journal Article
The major genetic risk factor for severe COVID-19 does not show any association among South Asian populations
Singh, Prajjval Pratap, Srivastava, Anshika, Sultana, Gazi Nurun Nahar, Khanam, Nargis, Pathak, Abhishek, Suravajhala, Prashanth, Singh, Royana, Shrivastava, Pankaj, van Driem, George, Thangaraj, Kumarasamy, Chaubey, Gyaneshwer
Published in Scientific reports (11.06.2021)
Published in Scientific reports (11.06.2021)
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Journal Article
Most frequent South Asian haplotypes of ACE2 share identity by descent with East Eurasian populations
Srivastava, Anshika, Pandey, Rudra Kumar, Singh, Prajjval Pratap, Kumar, Pramod, Rasalkar, Avinash Arvind, Tamang, Rakesh, van Driem, George, Shrivastava, Pankaj, Chaubey, Gyaneshwer
Published in PloS one (16.09.2020)
Published in PloS one (16.09.2020)
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Journal Article
Publisher Correction: The major genetic risk factor for severe COVID‑19 does not show any association among South Asian populations
Singh, Prajjval Pratap, Srivastava, Anshika, Sultana, Gazi Nurun Nahar, Khanam, Nargis, Pathak, Abhishek, Suravajhala, Prashanth, Singh, Royana, Shrivastava, Pankaj, van Driem, George, Thangaraj, Kumarasamy, Chaubey, Gyaneshwer
Published in Scientific reports (05.08.2021)
Published in Scientific reports (05.08.2021)
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Journal Article
In Silico Characterization of RNASEH2A Pathogenic Variants and Identification of Novel Splice Site Donor Variant c.549+1G>T in Indian Population
Nanjundagowda, Vykuntaraju K, Paikaraya, Swabhiman, Srinivasan, Varunvenkat M, Srivastava, Anshika
Published in Curēus (Palo Alto, CA) (13.06.2023)
Published in Curēus (Palo Alto, CA) (13.06.2023)
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Journal Article
Matrix Metalloproteinases in Coronary Artery Disease
Mittal, Balraj, Mishra, Avshesh, Srivastava, Anshika, Kumar, Surendra, Garg, Naveen
Published in Advances in Clinical Chemistry (2014)
Published in Advances in Clinical Chemistry (2014)
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Book Chapter
Journal Article
TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome
Werren, Elizabeth A, LaForce, Geneva R, Srivastava, Anshika, Perillo, Delia R, Li, Shaokun, Johnson, Katherine, Baris, Safa, Berger, Brandon, Regan, Samantha L, Pfennig, Christian D, de Munnik, Sonja, Pfundt, Rolph, Hebbar, Malavika, Jimenez-Heredia, Raúl, Karakoc-Aydiner, Elif, Ozen, Ahmet, Dmytrus, Jasmin, Krolo, Ana, Corning, Ken, Prijoles, E J, Louie, Raymond J, Lebel, Robert Roger, Le, Thuy-Linh, Amiel, Jeanne, Gordon, Christopher T, Boztug, Kaan, Girisha, Katta M, Shukla, Anju, Bielas, Stephanie L, Schaffer, Ashleigh E
Published in Nature communications (22.02.2024)
Published in Nature communications (22.02.2024)
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Journal Article
An innovative technique for electronic transport model of group-III nitrides
Srivastava, Anshika, Saxena, Anshu, Saxena, Praveen K., Gupta, F. K., Shakya, Priyanka, Srivastava, Pankaj, Dixit, Manish, Gambhir, S., Shukla, R. K., Srivastava, A.
Published in Scientific reports (30.10.2020)
Published in Scientific reports (30.10.2020)
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Journal Article
Studying C-reactive protein and D-dimer levels in blood may prevent severe complications: A study in Bangladeshi COVID-19 patients
Sultana, Gazi Nurun Nahar, Srivastava, Anshika, Akhtaar, Khalida, Singh, Prajjval Pratap, Islam, Md Anarul, Mishra, Rahul Kumar, Chaubey, Gyaneshwer
Published in Frontiers in genetics (09.12.2022)
Published in Frontiers in genetics (09.12.2022)
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Journal Article
Dysregulation of cotranscriptional alternative splicing underlies CHARGE syndrome
Bélanger, Catherine, Bérubé-Simard, Félix-Antoine, Leduc, Elizabeth, Bernas, Guillaume, Campeau, Philippe M., Lalani, Seema R., Martin, Donna M., Bielas, Stephanie, Moccia, Amanda, Srivastava, Anshika, Silversides, David W., Pilon, Nicolas
Published in Proceedings of the National Academy of Sciences - PNAS (23.01.2018)
Published in Proceedings of the National Academy of Sciences - PNAS (23.01.2018)
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Journal Article
Report of four novel variants in ASNS causing asparagine synthetase deficiency and review of literature
Galada, Chelna, Hebbar, Malavika, Lewis, Leslie, Soans, Santosh, Kadavigere, Rajagopal, Srivastava, Anshika, Bielas, Stephanie, Girisha, Katta M., Shukla, Anju
Published in Congenital anomalies (01.09.2018)
Published in Congenital anomalies (01.09.2018)
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Journal Article
The peopling of Lakshadweep Archipelago
Mustak, Mohammed S, Rai, Niraj, Naveen, Mohan Rao, Prakash, Satya, Carlus, S Justin, Pasupuleti, Nagarjuna, Srivastava, Anshika, Singh, Prajjval Pratap, Babu, Idrees, Dubey, Pavan Kumar, Chaubey, Gyaneshwer, Thangaraj, Kumarasamy
Published in Scientific reports (06.05.2019)
Published in Scientific reports (06.05.2019)
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Journal Article
Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations
Werren, Elizabeth A, Peirent, Emily R, Jantti, Henna, Guxholli, Alba, Srivastava, Kinshuk Raj, Orenstein, Naama, Narayanan, Vinodh, Wiszniewski, Wojciech, Dawidziuk, Mateusz, Gawlinski, Pawel, Umair, Muhammad, Khan, Amjad, Khan, Shahid Niaz, Geneviève, David, Lehalle, Daphné, van Gassen, K L I, Giltay, Jacques C, Oegema, Renske, van Jaarsveld, Richard H, Rafiullah, Rafiullah, Rappold, Gudrun A, Rabin, Rachel, Pappas, John G, Wheeler, Marsha M, Bamshad, Michael J, Tsan, Yao-Chang, Johnson, Matthew B, Keegan, Catherine E, Srivastava, Anshika, Bielas, Stephanie L
Published in Cell death & disease (30.05.2024)
Published in Cell death & disease (30.05.2024)
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Journal Article