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VOLUME 17                                              CONTENTS                                              2017

VOLUME 17, Number 1                                                                                                                     MARCH 2017

 

INFORMATION ABOUT JOURNAL

 

Gengqian Zhang, Jinding Liu, Jiaqi Wang, Xiaojia Zhang, Xudong Wang, Junyi Shen and Deqing Chen • Evaluation of the Full-sibling Kinship Regarding Attendance of Multiple Full-siblings

1-10

DOI:10.31901/24566330.2017/17.01.01

[Abstract] [Full Text – PDF]

 

Bibhas Kar, S. Sivamani, J. Shajeev and K. Sivakumar • Unusual Hand Malformation with Cardiac Defect:  A Rare Presentation

11-14

DOI:10.31901/24566330.2017/17.01.02

[Abstract] [Full Text – PDF]

 

Jyot Amrita, Mridula Mahajan, A.J.S. Bhanwer, Gurinder Mohan and Kawaljit Matharoo • Peroxisome Proliferator Activated Receptor Gamma (PPARg) Pro12Ala Gene Polymorphism and Oxidative Stress in Menopausal Women with Cardiovascular Disease from North Indian Population of Punjab

15-25

DOI:10.31901/24566330.2017/17.01.03

[Abstract] [Full Text – PDF]

 

Sule Menziletoglu Yildiz, Gulizar Atli, Ersel Gulec, Birol Guvenc and Dilek Ozcengiz • Major Histocompatibility Complex Class I-related Chain  A and B Gene Expression in Sepsis Patient

26-30

DOI:10.31901/24566330.2017/17.01.04

[Abstract] [Full Text – PDF]

 

Amrin Shaikh and Divya Chandel • Biomonitoring Study on Workers Occupationally Exposed to Automobile Fuels

31-37

DOI:10.31901/24566330.2017/17.01.05

[Abstract] [Full Text – PDF]

 

J. Sumitha, T. Devi and D. Ravi • Comparative Study on Gene Expression for Detecting Diseases Using Optimized Algorithm

38-42

DOI:10.31901/24566330.2017/17.01.06

[Abstract] [Full Text – PDF]

 

Guide to Contributors

43-47

 

List of Members of the Editorial Board

48-50

 

VOLUME 17, Number 2                                                                                                                             JUNE 2017

 

Sibel Demir Ozturk, Atac Celik, Ayse Feyda Nursal, Akin Tekcan, Aydin Rustemoglu, Nevin Karakus and Serbulent Yigit • Importance of NPC1 Gene 644 A→G Mutation in Coronary Artery Disease

51-55

DOI:10.31901/24566330.2017/17.02.01

[Abstract] [Full Text – PDF]

 

Gayatri Kulkarni and Suvidya Ranade • Molecular Analysis of Hotspot Regions of ARX and MECP2 Genes in Intellectual Disability and Cornelia De Lange Syndrome

56-63

DOI:10.31901/24566330.2017/17.02.02

[Abstract] [Full Text – PDF]

 

E. G. Karahan, A. G. Tomatir, I. Acikbas, A. B. Er, F. Evyapan, B. Akdag and P. E. Arslan • Determination of Genotoxic Damage by Comet Assay in Smokers

64-71

DOI:10.31901/24566330.2017/17.02.03

[Abstract] [Full Text – PDF]

 

Parth S. Shah, Nidhi D. Shah, Hari Shankar P. Ray, Nikunj B. Khatri, Ketan K. Vaghasia, Sandip C. Shah and Mandava V. Rao • Compound Heterozygosity of  β-Thalassemia Traits of HBB Gene in a Family: A Case Report

72-75

DOI:10.31901/24566330.2017/17.02.04

[Abstract] [Full Text – PDF]

 

Sehra Birgόl Batmaz, Tugba Arikoglu, Nisa Uyar, Ibrahim Φmer Barlas and Semanur Kuyucu • The Effect of Vitamin D Pathway Genes on Asthma Susceptibility, Asthma Control and Vitamin D Levels in Turkish Asthmatic Children

76-85

DOI:10.31901/24566330.2017/17.02.05

[Abstract] [Full Text – PDF]

 

Fadime Mutlu Icduygu, Mujgan Ozdemir Erdogan, Sevinc Sarinc Ulasli, Handan Gonenli Yildiz, Zeynep Sonmez Celik, Mehmet Unlu and Mustafa Solak • Is There an Association Between NOD2 Gene Polymorphisms and Chronic Obstructive Pulmonary Disease Progression?

86-96

DOI:10.31901/24566330.2017/17.02.06

[Abstract] [Full Text – PDF]

 

VOLUME 17, Number 3                                                                                                                    SEPTEMBER 2017

 

Wittaya Jomoui • Novel Tag SNPs of Beta-Globin Gene Cluster in Chinese Han Population: Biological Marker for Genetic Backgrounds and Clinical Studies

97-102

DOI:10.31901/24566330.2017/17.03.01

[Abstract] [Full Text – PDF]

 

R. Nageshwari, M. Dhivakar, K. Balakrishnan, Sivan Arul Selvan and V. Kumaravel • Common CYP21A2 Gene Mutations in South Indian Congenital Adrenal Hyperplasia Patients

103-108

DOI:10.31901/24566330.2017/17.03.02

[Abstract] [Full Text – PDF]

 

Patricia Fenton-Navarro, Eduardo Pιrez-Campos, Marνa del Socorro Pina-Canseco and Bertha Fenton-Navarro • Gaucher’s Disease and Hurler’s Syndrome in Two First Cousins

109-117

DOI:10.31901/24566330.2017/17.03.03

[Abstract] [Full Text – PDF]

 

M. K. Dwivedi and Deepak Sinha • Role of MTHFR 677 C>T Polymorphism on Blood Homocysteine and Susceptibility to Hypertension

118-125

DOI:10.31901/24566330.2017/17.03.04

[Abstract] [Full Text – PDF]

 

A. Meyyazhagan, N. M. Raman, M. Easwaran, B. Balasubramanian, K. Alagamuthu, H. Kuchi Bhotla2, S. Shanmugam, K. Inbaraj  M. Ramesh Kumar, P. Kumar, L. Thangamani, S. Piramanayagam, V. Anand, Y. Mohd, S. Park, O. Teijido, J.C. Carril, P. Cacabelos, S. Keshavarao and R. Cacabelos • Biochemistry, Cytogenetics and DMD Gene Mutations in South Indian Patients with Duchenne Muscular Dystrophy

126-134

DOI:10.31901/24566330.2017/17.03.05

[Abstract] [Full Text – PDF]

 

Brief Communication

 

Warda Fatima, Saqib Mahmood, Shahida Hasnain, Nusrat Habib Rana, Nasar Sayeed Khan, Farooq Naeem and Muhammad Ayub • Parental Consanguineous Marriages are Associated with Early Age of Onset of Schizophrenia in a Pakistani Cohort

135-139

DOI:10.31901/24566330.2017/17.03.06

[Abstract] [Full Text – PDF]

 

Vipin Gupta and Gagandeep Kaur Walia • Genomics of Type 2 Diabetes Mellitus and Glycemic Traits

140-144

DOI:10.31901/24566330.2017/17.03.07

[Abstract] [Full Text – PDF]

 

VOLUME 17, Number 4                                                                                                                    DECEMBER 2017

 

Payam Shahnazi Gerdehsang, Najmeh Ranji, Mojtaba Gorji, Safoura Pakizehkar, Ali Asghar Kiani and Saeed Veysi • New Mutations in APC gene Among Familial Adenomatous Polyposis (FAP) Patients in Iran

145-150

DOI:10.31901/24566330.2017/17.04.01

[Abstract] [Full Text – PDF]

 

Bhuvnesh Yadav, Ajay Balayan, T. D. Dogra and Anupuma Raina • Genetic Ancestry of Delhi Population Inferred from Autosomal Short Tandem Repeats: Genetic Diversity Analysis

151-157

DOI:10.31901/24566330.2017/17.04.02

[Abstract] [Full Text – PDF]

 

Pranami Bhaumik, Priyanka Ghosh, Atanu Biswas, Sujoy Ghosh, Sandip Pal, Biswanath Sarkar and Subrata Kumar Dey  • Rare Intronic Variations in TP73 Gene Found in Patients  with Alzheimer’s Disease

158-168

DOI:10.31901/24566330.2017/17.04.03

[Abstract] [Full Text – PDF]

 

Vijayashree Priyadharsini Jayaseelan, Karthikeyan Muthusamy, Shridevi Venkatramani, Paramasivam Arumugam, Jayaraman Gopalswamy and Santhiya Sathiyavedu Thiagarajan • Gender-specific Association of ATP2B1 (rs2681472) Gene Polymorphism with Essential Hypertension in South Indian Population

169-176

DOI:10.31901/24566330.2017/17.04.04

[Abstract] [Full Text – PDF]

 

Soundarya Priya Alexandar, Indhumathi Dhinakaran, Vidhya Ravi, Nandhini Parthasarathy, Somasundari Ganesan, Muthumeenakshi Bhaskaran and Ganesh Prasad Arun Kumar • Meta-Analysis of Association of Mitochondrial DNA Mutations  with Type 2 Diabetes and Gestational Diabetes Mellitus

177-190

DOI:10.31901/24566330.2017/17.04.05

[Abstract] [Full Text – PDF]

 

Index

191-193

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