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Novel genetic association of the Furin gene polymorphism rs1981458 with COVID-19 severity among Indian populations
Novel genetic association of the Furin gene polymorphism rs1981458 with COVID-19 severity among Indian populations
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Novel genetic association of the Furin gene polymorphism rs1981458 with COVID-19 severity among Indian populations

Scientific reports, 2024-04, Vol.14 (1), p.7822-7822 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. corrected publication 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2024 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-024-54607-7 ;PMID: 38570613

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2
Atomistic nonlinear carrier dynamics in Ge
Atomistic nonlinear carrier dynamics in Ge
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Atomistic nonlinear carrier dynamics in Ge

Scientific reports, 2023-04, Vol.13 (1), p.5630-5630, Article 5630 [Peer Reviewed Journal]

2023. The Author(s). ;The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2023 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-023-32732-z ;PMID: 37024661

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3
Homozygous p.(Glu87Lys) variant in ISCA1 is associated with a multiple mitochondrial dysfunctions syndrome
Homozygous p.(Glu87Lys) variant in ISCA1 is associated with a multiple mitochondrial dysfunctions syndrome
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Homozygous p.(Glu87Lys) variant in ISCA1 is associated with a multiple mitochondrial dysfunctions syndrome

Journal of human genetics, 2017-07, Vol.62 (7), p.723-727 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jul 2017 ;The Japan Society of Human Genetics 2017. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2017.35 ;PMID: 28356563

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4
Genetic Association of ACE2 rs2285666 Polymorphism With COVID-19 Spatial Distribution in India
Genetic Association of ACE2 rs2285666 Polymorphism With COVID-19 Spatial Distribution in India
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Genetic Association of ACE2 rs2285666 Polymorphism With COVID-19 Spatial Distribution in India

Frontiers in genetics, 2020-09, Vol.11, p.564741-564741 [Peer Reviewed Journal]

Copyright © 2020 Srivastava, Bandopadhyay, Das, Pandey, Singh, Khanam, Srivastava, Singh, Dubey, Pathak, Gupta, Rai, Sultana and Chaubey. ;Copyright © 2020 Srivastava, Bandopadhyay, Das, Pandey, Singh, Khanam, Srivastava, Singh, Dubey, Pathak, Gupta, Rai, Sultana and Chaubey. 2020 Srivastava, Bandopadhyay, Das, Pandey, Singh, Khanam, Srivastava, Singh, Dubey, Pathak, Gupta, Rai, Sultana and Chaubey ;ISSN: 1664-8021 ;EISSN: 1664-8021 ;DOI: 10.3389/fgene.2020.564741 ;PMID: 33101387

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5
The major genetic risk factor for severe COVID-19 does not show any association among South Asian populations
The major genetic risk factor for severe COVID-19 does not show any association among South Asian populations
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The major genetic risk factor for severe COVID-19 does not show any association among South Asian populations

Scientific reports, 2021-06, Vol.11 (1), p.12346-12346, Article 12346 [Peer Reviewed Journal]

The Author(s) 2021. corrected publication 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021, corrected publication 2021 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-91711-4 ;PMID: 34117310

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6
Most frequent South Asian haplotypes of ACE2 share identity by descent with East Eurasian populations
Most frequent South Asian haplotypes of ACE2 share identity by descent with East Eurasian populations
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Most frequent South Asian haplotypes of ACE2 share identity by descent with East Eurasian populations

PloS one, 2020-09, Vol.15 (9), p.e0238255-e0238255 [Peer Reviewed Journal]

COPYRIGHT 2020 Public Library of Science ;COPYRIGHT 2020 Public Library of Science ;2020 Srivastava et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2020 Srivastava et al 2020 Srivastava et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0238255 ;PMID: 32936832

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7
Publisher Correction: The major genetic risk factor for severe COVID‑19 does not show any association among South Asian populations
Publisher Correction: The major genetic risk factor for severe COVID‑19 does not show any association among South Asian populations
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Publisher Correction: The major genetic risk factor for severe COVID‑19 does not show any association among South Asian populations

Scientific reports, 2021-08, Vol.11 (1), p.16296-16296, Article 16296 [Peer Reviewed Journal]

The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-94864-4 ;PMID: 34354116

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8
In Silico Characterization of RNASEH2A Pathogenic Variants and Identification of Novel Splice Site Donor Variant c.549+1G>T in Indian Population
In Silico Characterization of RNASEH2A Pathogenic Variants and Identification of Novel Splice Site Donor Variant c.549+1G>T in Indian Population
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In Silico Characterization of RNASEH2A Pathogenic Variants and Identification of Novel Splice Site Donor Variant c.549+1G>T in Indian Population

Curēus (Palo Alto, CA), 2023-06, Vol.15 (6), p.e40366-e40366 [Peer Reviewed Journal]

Copyright © 2023, Nanjundagowda et al. ;Copyright © 2023, Nanjundagowda et al. This work is published under https://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Copyright © 2023, Nanjundagowda et al. 2023 Nanjundagowda et al. ;ISSN: 2168-8184 ;EISSN: 2168-8184 ;DOI: 10.7759/cureus.40366 ;PMID: 37456470

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9
Matrix Metalloproteinases in Coronary Artery Disease
Matrix Metalloproteinases in Coronary Artery Disease
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Matrix Metalloproteinases in Coronary Artery Disease

Advances in Clinical Chemistry, 2014, Vol.64, p.1-72 [Peer Reviewed Journal]

2014 Elsevier Inc. ;ISSN: 0065-2423 ;ISBN: 9780128002636 ;ISBN: 0128002638 ;EISSN: 2162-9471 ;DOI: 10.1016/B978-0-12-800263-6.00001-X

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10
An Innovative Model for Electronic Band Structure Analysis of Doped and Un-Doped ZnO
An Innovative Model for Electronic Band Structure Analysis of Doped and Un-Doped ZnO
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An Innovative Model for Electronic Band Structure Analysis of Doped and Un-Doped ZnO

Journal of electronic materials, 2021-04, Vol.50 (4), p.2417-2424 [Peer Reviewed Journal]

The Minerals, Metals & Materials Society 2021 ;The Minerals, Metals & Materials Society 2021. ;ISSN: 0361-5235 ;EISSN: 1543-186X ;DOI: 10.1007/s11664-021-08756-4

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11
TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome
TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome
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TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome

Nature communications, 2024-02, Vol.15 (1), p.1640-1640 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-024-45948-y ;PMID: 38388531

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12
An innovative technique for electronic transport model of group-III nitrides
An innovative technique for electronic transport model of group-III nitrides
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An innovative technique for electronic transport model of group-III nitrides

Scientific reports, 2020-10, Vol.10 (1), p.18706-18706, Article 18706 [Peer Reviewed Journal]

The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-75588-3 ;PMID: 33127982

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13
Dysregulation of cotranscriptional alternative splicing underlies CHARGE syndrome
Dysregulation of cotranscriptional alternative splicing underlies CHARGE syndrome
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Dysregulation of cotranscriptional alternative splicing underlies CHARGE syndrome

Proceedings of the National Academy of Sciences - PNAS, 2018-01, Vol.115 (4), p.E620-E629 [Peer Reviewed Journal]

Volumes 1–89 and 106–114, copyright as a collective work only; author(s) retains copyright to individual articles ;Copyright National Academy of Sciences Jan 23, 2018 ;2018 ;ISSN: 0027-8424 ;EISSN: 1091-6490 ;DOI: 10.1073/pnas.1715378115 ;PMID: 29311329

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14
Studying C-reactive protein and D-dimer levels in blood may prevent severe complications: A study in Bangladeshi COVID-19 patients
Studying C-reactive protein and D-dimer levels in blood may prevent severe complications: A study in Bangladeshi COVID-19 patients
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Studying C-reactive protein and D-dimer levels in blood may prevent severe complications: A study in Bangladeshi COVID-19 patients

Frontiers in genetics, 2022-12, Vol.13, p.966595-966595 [Peer Reviewed Journal]

Copyright © 2022 Sultana, Srivastava, Akhtaar, Singh, Islam, Mishra and Chaubey. ;Copyright © 2022 Sultana, Srivastava, Akhtaar, Singh, Islam, Mishra and Chaubey. 2022 Sultana, Srivastava, Akhtaar, Singh, Islam, Mishra and Chaubey ;ISSN: 1664-8021 ;EISSN: 1664-8021 ;DOI: 10.3389/fgene.2022.966595 ;PMID: 36568370

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15
Author Correction: Novel genetic association of the Furin gene polymorphism rs1981458 with COVID-19 severity among Indian populations
Author Correction: Novel genetic association of the Furin gene polymorphism rs1981458 with COVID-19 severity among Indian populations
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Author Correction: Novel genetic association of the Furin gene polymorphism rs1981458 with COVID-19 severity among Indian populations

Scientific reports, 2024-04, Vol.14 (1), p.9523-9523 [Peer Reviewed Journal]

The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-024-60182-8 ;PMID: 38664564

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16
Significant role of estrogen and progesterone receptor sequence variants in gallbladder cancer predisposition: a multi-analytical strategy
Significant role of estrogen and progesterone receptor sequence variants in gallbladder cancer predisposition: a multi-analytical strategy
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Significant role of estrogen and progesterone receptor sequence variants in gallbladder cancer predisposition: a multi-analytical strategy

PloS one, 2012-07, Vol.7 (7), p.e40162-e40162 [Peer Reviewed Journal]

COPYRIGHT 2012 Public Library of Science ;COPYRIGHT 2012 Public Library of Science ;2012 Srivastava et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Srivastava et al. 2012 ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0040162 ;PMID: 22808109

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17
The peopling of Lakshadweep Archipelago
The peopling of Lakshadweep Archipelago
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The peopling of Lakshadweep Archipelago

Scientific reports, 2019-05, Vol.9 (1), p.6968-6968, Article 6968 [Peer Reviewed Journal]

The Author(s) 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2019 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-019-43384-3 ;PMID: 31061397

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18
Genetic and linguistic non-correspondence suggests evidence for collective social climbing in the Kol tribe of South Asia
Genetic and linguistic non-correspondence suggests evidence for collective social climbing in the Kol tribe of South Asia
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Genetic and linguistic non-correspondence suggests evidence for collective social climbing in the Kol tribe of South Asia

Scientific reports, 2020-03, Vol.10 (1), p.5593-5593, Article 5593 [Peer Reviewed Journal]

The Author(s) 2020 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-020-61941-z ;PMID: 32221319

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19
A study of the alteration in hematological parameters and liver function test with respect to the severity of dengue fever
A study of the alteration in hematological parameters and liver function test with respect to the severity of dengue fever
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A study of the alteration in hematological parameters and liver function test with respect to the severity of dengue fever

Asian Journal of Medical Sciences, 2021-03, Vol.12 (3), p.93-97 [Peer Reviewed Journal]

ISSN: 2467-9100 ;EISSN: 2091-0576 ;DOI: 10.3126/ajms.v12i3.33027

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20
PERFORMANCE INVESTIGATION OF FULLY VERTICAL ORGANIC MATERIAL BASED MULTI-LAYER OLEDs
PERFORMANCE INVESTIGATION OF FULLY VERTICAL ORGANIC MATERIAL BASED MULTI-LAYER OLEDs
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PERFORMANCE INVESTIGATION OF FULLY VERTICAL ORGANIC MATERIAL BASED MULTI-LAYER OLEDs

I-Manager's Journal on Material Science, 2018, Vol.5 (4), p.23

2018 i-manager publications. All rights reserved. ;ISSN: 2347-2235 ;EISSN: 2347-615X ;DOI: 10.26634/jms.5.4.13969

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