Page 122 - Annual report 2021-22
P. 122

Annual Report 2021-22 |


                                                                                                     6.922
                   105.       Genetic  risk  prediction  of  COVID-19  susceptibility  and  severity  in  the  Indian
                       population. Prakrithi P, Lakra P, Sundar D, Kapoor M, Mukerji M, Gupta I, The Indian Genome
                       Variation Consortium. FRONTIERS IN GENETICS;2021;12;714185 [Journal Article]
                                                                                                     4.274
                   106.       Transthyretin and Receptor for advanced glycation end product's differential levels    105

                       associated  with  the  pathogenesis  of  rheumatoid  Arthritis.  Monu  ,  Agnihotri  P,  Saquib  M,
                       Sarkar  A,  Chakraborty  D,  Kumar  U, Biswas  S*.  J  INFLAMM  RES  28;14:5581-5596  [Journal
                       Article]
                                                                                                      6.92
                   107.       Cilostazol  attenuated  prenatal  valproic  acid-induced  behavioural  and  biochemical
                       deficits in a rat model of autism spectrum disorder. Luhach K, Kulkarni GT, Singh VP, Sharma
                       B. THE JOURNAL OF PHARMACY AND PHARMACOLOGY;2021 OCT 7;11;73;1460-1469 [Journal
                       Article]
                                                                                                     3.765
                   108.       Cortical and subcortical brain area atrophy in SCA1 and SCA2 patients in India: The
                       structural  MRI  underpinnings  and  correlative  insight  among  the  atrophy  and  disease
                       attributes. Tamuli D, Kaur M, Sethi T, Singh A, Faruq M, Jaryal AK, Srivastava AK, Kumaran SS,
                       Deepak KK. NEUROLOGY INDIA;2021 SEP-OCT;5;69;1318-1325 [Journal Article]
                                                                                                     2.117
                   109.       A founder mutation in the GMPPB gene [c.1000G > A (p.Asp334Asn)] causes a mild
                       form  of  limb-girdle  muscular  dystrophy/congenital  myasthenic  syndrome  (LGMD/CMS)  in
                       South Indian patients. Polavarapu K, Mathur A, Joshi A, Nashi S, Preethish-Kumar V, Bardhan
                       M,  Sharma  P,  Parveen  S,  Seth  M,  Vengalil  S,  Chawla  T,  Shingavi  L,  Shamim  U,  Nayak  S,
                       Vivekanand A, Töpf A, Roos A, Horvath R, Lochmüller H, Nandeesh B, Arunachal G, Nalini A,
                       Faruq M. NEUROGENETICS;2021 OCT;4;22;271-285 [Journal Article]
                                                                                                      2.75
                   110.       Global, regional, and national mortality among young people aged 10-24 years, 1950-

                       2019:  a  systematic  analysis  for  the  Global  Burden  of  Disease  Study  2019.    GBD  2019
                       Adolescent Mortality Collaborators (Ward JL, … Agarwal A, … Patton GC, Vine RM. LANCET
                       2021 Oct 30; 398(10311): 1593–1618 [JOURNAL ARTICLE]
                                                                                                     202.7
                   111.       Therapeutic Role of sirtuins targeting unfolded protein response, coagulation, and
                       inflammation in hypoxia-induced thrombosis. Sadia K, Ashraf MZ, Mishra A. FRONTIERS IN
                       PHYSIOLOGY;2021;12;733453 [Review]
                                                                                                     4.566
                   112.       A  multifactorial  assessment  of  the  SRP  pathway  constituent  FtsY  as  a  vital
                       mycobacterial  constituent.  Shivangi,  Meena  LS.  BIOTECHNOLOGY  AND  APPLIED
                       BIOCHEMISTRY;2021 NOV 27; [Journal Article]
                                                                                                     2.431
                   113.       Mass  spectrometry-based  lipidomic  analysis  reveals  altered  lipid  profile  in  brain
                       tissues resected from patients with focal cortical dysplasia (FCD). Kumar K, Yadav N, Banerjee
                       J,  Tripathi  M,  Sharma  MC,  Lalwani  S,  Siraj  F,  Chandra  PS,  Sengupta  S,  Dixit  AB.  EPILEPSY
                       RESEARCH;2021 NOV;177;106773 [Journal Article]
                                                                                                     3.045
   117   118   119   120   121   122   123   124   125   126   127