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Dr Saadi Abdul Vahab

vidwan id: 55154
Male

Associate Professor, Department of Biotechnology
Manipal Academy of Higher Education, Manipal

Expertise

  • Genetics and Heredity

Publications

Total Articles 24
Books 0
Proceedings 0

Publications

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Scopus

Citations 392
h-index 9

CrossRef

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Citations 385
h-index 9
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Professional Recognition

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Community & Membership

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Society Of Biological Chemists, India

Life Member

Society for Mitochondrial Research and Medicine, India

Life Member

International Society for Heart Research (ISHR)

Life Member

Bio

Molecular Diagnostic Research and Molecular Genetics of Human Diseases

Personal Details

  • Male
  • Associate Professor , Manipal Academy of Higher Education, Manipal
  • Department of Biotechnology, Manipal Academy of Higher Education
Post Doctorate
Other Institute 2003
Ph.D.
Other Institute 2000
Associate Professor Aug 2005 – Present
Manipal Academy of Higher Education, Manipal | Department of Biotechnology

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Co-Authors (11)

ARSHIA

Dr ARSHIA ANGURAL

JSS Academy of Higher Education & Research

Himanshu

Dr Himanshu Gupta

GLA University, Mathura

Krishnamurthy

Dr Krishnamurthy Bhat

Manipal College of Pharmaceutical Sciences, Manipal

K

Prof K Satyamoorthy

Shri Dharmasthala Manjunatheshwara University

Banerjee

Dr Banerjee Moinak

Rajiv Gandhi Centre for Biotechnology

Shama Prasada

Prof Shama Prasada Kabekkodu

Manipal Academy of Higher Education, Manipal

T G

Dr T G Vasudevan

Shri Dharmasthala Manjunatheshwara University

Kumarasamy

Dr Kumarasamy Thangaraj

CSIR-Centre for Cellular and Molecular Biology

Vasudeva

Dr Vasudeva Guddattu

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Scholarly Work

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Scholarly Publications

Analysis of cosegregation of intragenic DNA sequence variations as markers of maternal cell contamination in prenatal diagnosis of β-thalassemia

Open Access
Article

Allele, genotype, and composite genotype effects of IL-1A +4845 and IL-1B +3954 polymorphisms for chronic periodontitis in an Indian population

Open Access
Article
Authors: Gayathri R.;Saadi A.V.;Mahalinga Bhat K.;Bhat S.G.;Satyamoorthy K.

Hypoplasia/aplasia of pelvis, femora, fibulae, ulna, digits and nails: Fuhrmann syndrome without WNT7A mutations

Open Access
Article
Authors: Girisha K.;Vasudevan T.;Saadi A.;Shah H.;Gopinath P.;Satyamoorthy K.

Thiopurine S-methyltransferase alleles, TPMT*2, *3B, and *3C, and genotype frequencies in an indian population

Open Access
Article
Authors: Murugesan R.;Saadi A.;Patra S.;Rao R.;Rao J.;Rai P.;Gopinath P.;Satyamoorthy K.

Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis

Open Access
Letter
Authors: Girisha K.;Vahab S.;Dalal A.;Gopinath P.;Satyamoorthy K.

Quantitative fluorescence polymerase chain reaction (QF-PCR) for prenatal diagnosis of chromosomal aneuploidies

Open Access
Article

Analysis of genotype and haplotype effects of ABCB1 (MDR1) polymorphisms in the risk of medically refractory epilepsy in an indian population

Open Access
Article
Authors: Vahab S.A.;Sen S.;Ravindran N.;Mony S.;Mathew A.;Vuayan N.;Nayak G.;Bhaskaranand N.;Banerjee M.;Satyamoorthy K.

Novel deletions in MYH7 and MYBPC3 identified in Indian families with familial hypertrophic cardiomyopathy

Open Access
Article