Ministry of Education
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Dr Shivaram Shastri

vidwan id: 234461
Male

Scientist, Department of Pediatrics
All India Institute of Medical Sciences (AIIMS), Delhi

Orchid Icon 0000-0003-1733-4579 Google Scholar Icon 7004455094 Researcher Icon D-5092-2011 Google Scholar Icon T-t8w6oAAAAJ

Expertise

  • Genetics and Heredity

Publications

Total Articles 37
Books 0
Proceedings 0

Publications

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Scopus

Citations 697
h-index 15

CrossRef

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Citations 252
h-index 10
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Professional Recognition

2004

Young Scientist

ISHG

Community & Membership

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Bio

Cftr Gene Mutations In Indian Patients With Cystic Fibrosis

Personal Details

  • Male
  • Scientist , All India Institute of Medical Sciences (AIIMS), Delhi
  • Department of Pediatrics, All India Institute of Medical Sciences, New Delhi
Ph.D.
All India Institute of Medical Sciences 2004
Scientist Nov 2012 – Present
All India Institute of Medical Sciences (AIIMS), Delhi | Department of Pediatrics

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Co-Authors (9)

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Prof Anuranjan Anand

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Dr Anil Kumar

G D Goenka University, Gurgaon

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Dr Joseph Mathew

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Scholarly Work

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Scholarly Publications

Glutaric acidemia type 1-clinico-molecular profile and novel mutations in gcdh gene in Indian patients

Open Access
Book Chapter
JIMD Reports. Year: 2015. Volume: 21 , Pages: 45-55 .
Authors: Gupta N.;Singh P.K.;Kumar M.;Shastri S.;Gulati S.;Kumar A.;Agarwala A.;Kapoor S.;Nair M.;Sapra S.;Dubey S.;Singh A.;Kaur P.;Kabra M.
DOI 10.1007/8904_2014_377
19 27

Clinical and mutation profile of children with cystic fibrosis in Jammu and Kashmir

Open Access
Article
Indian Pediatrics. Year: 2014. Volume: 51 , Issue: 3 , Pages: 185-189 .
Authors: Kawoosa M.;Bhat M.;Ali S.;Hafeez I.;Shastri S.
DOI 10.1007/s13312-014-0381-4
14 12

TMC1 may be a common gene for nonsyndromic hereditary hearing loss in Indian population

Open Access
article
Molecular Cytogenetics. Year: 2014. Volume: 7 , Pages: P70 .
Authors: Pawan Kumar Singh ., Shipra Sharma ., Manju Ghosh ., Shivaram S Shastri ., Neerja Gupta ., Madhumita Roy Chowdhury ., Madhulika Kabra .,
DOI 10.1186/1755-8166-7-s1-p70

Erratum to: Glutaric Acidemia Type 1-Clinico-Molecular Profile and Novel Mutations in GCDH Gene in Indian Patients

Open Access
incollection
Year: 2014. Pages: 129--129 .
Authors: Gupta, Neerja and Singh, Pawan Kumar and Kumar, Manoj and Shastri, Shivaram and Gulati, Sheffali and Kumar, Atin and Agarwala, Anuja and Kapoor, Seema and Nair, Mohandas and Sapra, Savita and others

Norrie disease: First mutation report and prenatal diagnosis in an indian family

Open Access
Article
Year: 2012. Volume: 79 , Issue: 11 , Pages: 1529-1531 .
Authors: Ghosh M.;Sharma S.;Shastri S.;Arora S.;Shukla R.;Gupta N.;Deka D.;Kabra M.
DOI 10.1007/s12098-012-0788-7
3 4

Association of angiotensin-converting enzyme insertion(I)/deletion (D) genotype in alzheimer's disease patients of north indian population

Open Access
Article
International Journal of Neuroscience. Year: 2011. Volume: 121 , Issue: 10 , Pages: 557-561 .
Authors: Nirmal S.;Tripathi M.;Shastri S.S.;Sagar R.;Vivekanandhan S.
DOI 10.3109/00207454.2011.591513
10 11

Idiopathic chronic pancreatitis in India: Phenotypic characterisation and strong genetic susceptibility due to SPINK1 and CFTR gene mutations

Open Access
Article
Year: 2010. Volume: 59 , Issue: 6 , Pages: 800-807 .
Authors: Midha S.;Khajuria R.;Shastri S.;Kabra M.;Garg P.
DOI 10.1136/gut.2009.191239
110

Long-term daily high and low doses of azithromycin in children with cystic fibrosis: A randomized controlled trial

Open Access
Article
Journal of Cystic Fibrosis. Year: 2010. Volume: 9 , Issue: 1 , Pages: 17-23 .
Authors: Kabra S.K.;Pawaiya R.;Lodha R.;Kapil A.;Kabra M.;Vani A.S.;Agarwal G.;Shastri S.S.
DOI 10.1016/j.jcf.2009.09.001
28 32