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List will be updated on 14th and 28th of Every Month
LIST OF PAPERS – PRESENT STATUS
REFERENCE
NO. IJHG- 501 - 600
REF. NO. IJHG-530
PAPER UNDER PRO
A Case-Control Association Study of Single Nucleotide Polymorphism C1858T of the PTPN22 Gene with Type-1 Diabetes in North Indian Population
Badaruddoza and Ishpreet Kaur Biji
Department of Human Genetics, Guru Nanak Dev University, Amritsar 143 005, Punjab, India
REF. NO. IJHG-533
PAPER UNDER PRO
Complex Mutation in methyl CpG Binding Protein 2 (MECP2) Gene in an Indian Patient with Rett Syndrome
Dhanjit Kumar Dasa, c, Vikas Ghattargia, Bhakti Mehtaa and Vrajesh Udanib,
aGenetic Research Centre, National Institute for Research in Reproductive Health (ICMR), Jahangir Merwanji Street, Parel, Mumbai 400 012, Maharashtra, India
bDepartment of Pediatric Neurology, Hinduja National Hospital and Research Centre, Mahim, Mumbai 400 016, Maharashtra, India
REF. NO. IJHG-535
PAPER UNDER PRO
Perrault Syndrome: Indication of Progressive Mutations Causing Ovarian Dysgenesis and Sensorineural Hearing Loss
Shivang Parikh and Hitesh Mehta
Department of Medical Biotechnology, Shree P. M. Patel Institute of Integrated M.Sc. in Biotechnology, Anand 388 001, Gujarat, India
REF. NO. IJHG-552
PAPER UNDER PROCESSING
Effect of the TNF Α-308 Polymorphism on Birth Outcomes among South African Women
Poovendhree Reddy1, Rajen N Naidoo2, Anil Chuturgoon3, Kareshma Asharam2, Alisa Phulukdaree3 and Shivona Gounden3
1Department of Community Health Studies, Durban University of Technology, Durban, South Africa
2Discipline of Occupational and Environmental Health, School of Nursing and Public Health, 3Discipline of Medical Biochemistry, School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Durban, South Africa
REF. NO. IJHG-562
PAPER UNDER PROCESSING
The G 1462A and G 1473A in the 12S Rrna Mitochondrial DNA in Congenital Non-Syndromic Sensorineural
Sutji Pratiwi Rahardjo
Department of Ear, Nose and Throat, Medical Faculty of Hasanuddin University, Makassar, South Sulawesi-Indonesia 90133
REF. NO. IJHG-566
PAPER UNDER PROCESSING
Oro-Facio-Digital Syndrome Type IX With Polydactyly and Multiple Intraocular Findings
N. E. Gaboon1,3 and J. Y. Al-Aama1,2
1,2Department of Genetic Medicine, Faculty of Medicine, 2Princess Al-Jawhara Al-Brahim Center of Excellence in Research of Hereditary Disorders, King Abdulaziz University Hospital, Jeddah, Kingdom of Saudi Arabia
3Medical Genetic Center, faculty of medicine, AinShams University, Cairo, Egypt
REF. NO. IJHG-570
PAPER FOR REVISION WITH AUTHOR
The Association of Sport Performance with Alpha Actinin 3 Gene R577X Polymorphism
Bade Yamak1 Melek Yuce2 Hasan Bagci2 and Osman Imamoglu1
1 Ondokuz Mayis University Yasar Dogu Faculty of Sport Sciences
2Ondokuz Mayis University Department of Medical Biology
REF. NO. IJHG-571
PAPER UNDER PROCESSING
Alu Insertion/Deletion Polymorphism in the Tribes of South India
A. Krishnaveni* and K. Prabhakaran
PG & Research Department of Zoology, Periyar E V R College (Autonomous), Tiruchirappalli 620 023, Tamil Nadu, India
REF. NO. IJHG-573
PAPER FOR REVISION WITH AUTHOR
Mthfr and IL-4 Gene Polymorphisms are not Associated with Primary Dysmenorrhea in Young Adults
Asker Zeki Ozsoy1, Bulent Cakmak1, Mehmet Can Nacar1, Ali Cetin2, Fazlı Demirturk1, Hatice Yılmaz Dogru1, Nevin Karakus3 and Serbulent Yigit3
1Departments of Obstetrics and Gynecology and 3Medical Biology, Gaziosmanpasa University Faculty of Medicine, Tokat; 2Department of Obstetrics and Gynecology, Cumhuriyet University Faculty of Medicine, Sivas, Turkey
REF. NO. IJHG-575
PAPER FOR REVISION WITH AUTHOR
Prevalence of Some Genetic Polymorphisms among Cardiovascular Patients Residing at High Altitude and Sea Level
Mohammed S. Al Saeed1, 2, Nabil S. Awad1,3,4* and Adel E. El-Tarras1,3,5
1High Altitude Research Center (HARC), Taif University, Saudi Arabia
2Department of Surgery, College of Medicine, Taif University, Saudi Arabia
3Biotechnology and Genetic Engineering Unit, Scientific Research Deanship, Taif University, Saudi Arabia
4Ain Shams University Center for Genetic Engineering and Biotechnology (ACGEB), Ain Shams University, Cairo, Egypt.
5Genetics Dep., Faculty of Agriculture, Cairo University, Cairo, Egypt.
REF. NO.
IJHG-576
PAPER UNDER PROCESSING
Decreased Hdac1 Gene Expression in Patients with Alzheimer’s Disease
Ali Bayram1, Feridun AKKAFA2, Ahmet OZER2, Remzi Yiğiter3
1Fırat University, Elazig High School of Health Sciences, Elazığ, Turkey
2Harran University Faculty of Medicine, Department of Medical Biology, Urfa, Turkey 3Gaziantep University Faculty of Medicine, Department of Neurology, Gaziantep, Turkey
REF. NO.
IJHG-577
PAPER UNDER PROCESSING
Risk Assessment of Occupational Exposure to Pesticides among Pesticide Distributors of Punjab (India) Using Single Cell Gel Electrophoresis
PrabhaSyall and PoojaChadha*
Dept of Zoology, Guru Nanak Dev University, Amritsar
REF.
NO. IJHG-578
PAPER UNDER PROCESSING
Adducin and Plasminogen Activator İnhibitor 1 Gene Polymorphisms in for a Coronary Artery By-Pass Surgery
Sefa Şenol1, Kürşat Kargün2, Ali Bayram2, Özlem Seçen1 and Berrin Ayaz Tüylü3
1Department of Cardiovascular Surgery, Educational and Resarch Hospital, Elazığ, Turkey
2Fırat University, Elazig High School of Health Sciences, Elazığ, Turkey
3Anadolu University, Department of Molecular Biology, Eskisehir, Turkey
REF. NO.
IJHG-579
PAPER UNDER PROCESSING
Endothelin-1 Gene Polymorphism in Preoperative Myocardial Infarction
Sefa Şenol2, İlker Akar3, Kürşat Kargün4, Ali Bayram4, Murat Kara5, Özlem Seçen2
2Department of Cardiovascular Surgery, Educational and Resarch Hospital, Elazığ, Turkey
3Gaziosmanpaşa University, School of Medicine, Department of Cardiovascular Surgery, Tokat, Turkey
4Fırat University, Elazig High School of Health Sciences, Elazığ, Turkey
5Mugla Sıtkı Koçman University, School of Medicine, Department of Genetic Medicine, Muğla, Turkey
REF. NO.
IJHG-580
PAPER UNDER PROCESSING
MRNA Expression of Nuclear Factor-Κb1 in Parkinson's Disease Patients
Ali Bayram2, Burak Uz3 and Remzi Yiğiter4
2Fırat University, Elazig High School of Health Sciences, Elazığ, Turkey
3Fırat University Faculty of Medicine, Department of Hematology, Elazığ, Turkey
4Gaziantep University Faculty of Medicine, Department of Neurology, Gaziantep, Turkey
REF. NO.
IJHG-581
PAPER UNDER PROCESSING
Case Report: Y Chromosome Microdeletion in a Infertile Patient with Mosaic Klinefelter Syndrome (46,XY/47,XXY)
Mehmet Cetinkaya1, Mehmet Kaba2, Esin Sakalli Cetin3 and Sukru Candan4
1Department of Urology, Faculty of Medicine, Mugla Sitki Kocman University, Mugla,Turkey, 48000
2Department of Urology, Faculty of Medicine, Yuzuncu Yil University, Van, Turkey 65080
3Department of Medical Biology, Faculty of Medicine, Mugla Sitki Kocman University, Mugla, Turkey, 48000
4Department of Medical Genetics, Atatürk State Hospital, Balıkesir, Turkey, 10100
REF. NO.
IJHG-582
PAPER UNDER PROCESSING
Knowledge, Awareness and Participation of Medical and Non Medical Students in the Malaysia National Thalassemia Prevention Programme
Vasudeva Murthy.C.R1.1,Muhammad ZarifAsraf Bin Zulkeflle2, Sunil Pazhayanur Venkateswaran3 and Ankur Barua4
1,3Department of Pathology, 4Department of Community Medicine, International Medical University, Kuala Lumpur, Malaysia
2Biomedical science graduate, Management and Science University, Shah Alam, Malaysia
REF. NO. IJHG-583
PAPER UNDER PROCESSING
Mutations Analysis of the Growth Differentiation Factor 9 Gene in Syrian Women with Ovarian Failure
Rana Al-Ajoury1, Essam Kassem1, Bassel Al-Halabi2, Faten Moassess2, Hossam Murad2 and Walid Al-Achkar2
1Department of Biology, Faculty of Science, Damascus University, Syria
2Department of Molecular Biology and Biotechnology, Division of Human Genetics, Atomic Energy Commission of Syria, Damascus, Syria
REF. NO. IJHG-584
PAPER FOR REVISION WITH AUTHOR
Significance of Cytogenetic and Molecular Analysis in Primary Amenorrhea
Merin M. Thomas & Rema Devi
St. John’s Medical College, Division of Human Genetics, Department of Anatomy, Bangalore – 34 Karnataka
REF. NO.
IJHG-585
PAPER UNDER PROCESSING
Evaluation of Galectin-3 Genetic Variants and Its Serum Levels in Rheumatoid Arthritis in North India
Tarnjeet Kaur1, Annie Sodhi1, Jatinder Singh2, Sumeet Arora3, Sukhdev Singh Kamboj2 and Manpreet Kaur1*
1Department of Human Genetics, Guru Nanak Dev University, Amritsar-143005 (Punjab), India
2Department of Molecular Biology and Biochemistry, Guru Nanak Dev University, Amritsar-143005 (Punjab), India
3Medical & Arthritis Care Centre, Amritsar-143001 (Punjab), India
REF. NO. IJHG-586
PAPER FOR REVISION WITH AUTHOR
Forensic Identification by Using Insertion- Deletion Polymorphisms
Lim Fuey Jia1, Vasudeva Murthy2, Vijaya Paul Samuel3 and Kumaraswamy Kademane4
1Biomedical Science Programme, 2,4Department of Pathology, 3Department of Human Biology, International Medical University, Malaysia
REF. NO. IJHG-587
PAPER UNDER PROCESSING
The Relationship between Single Nucleotide Polymorphisms of the Filaggrin Gene and Atopic Dermatitis-Associated Minor Features
Myungshin Kim1,2, Joonhong Park1,2, Jiyeon Kim2, Yonggoo Kim1,2, Mi Sun Park3, Eujin Cho4, Kyung Eun Jung4, Hei Sung Kim4 and Young Min Park4
1Department of Laboratory Medicine, College of Medicine, the Catholic University of Korea, Seoul, Korea
2Catholic Genetic Laboratory Center, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea
3Department of Biostatistics, Clinical Research Coordinating Center, the Catholic University of Korea, Republic of Korea, Seoul, Korea
4Department of Dermatology, College of Medicine, the Catholic University of Korea, Seoul, Korea
REF. NO. IJHG-590
PAPER UNDER PROCESSING
Congenital Heart Defects and Chromosomal Abnormality
Sayee Rajangam1, Preetha Tilak2 and Sonia Dhawan3
Division of Human Genetics, Department of Anatomy, St John’s Medical College, Bangalore 560034
REF. NO. IJHG-591
PAPER UNDER PROCESSING
Two Independent Origins of Β+-Thalassemia Due To -31 A to G Mutation
Worrawalan Lerttham1,2, Goonnapa Fucharoen2, Supawadee Yamsri2 and Supan Fucharoen2
1Medical Science Program, Graduate School, Khon Kaen University, Thailand
2Centre for Research and Development of Medical Diagnostic Laboratories, Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, Thailand
REF. NO. IJHG-592
PAPER UNDER PROCESSING
Evaluation of SNPs in the Mitochondrial DNA Using Nano Chip Microarray in Turkish Population
Melahat Kurtuluş-Ülküer1, Uner Ulkuer2 and Ibrahim Baris3
1Department of Pharmaceutical Microbiology, Faculty of Pharmacy, University of Gazi, Ankara, Turkey
2General Directorate of Security, Ankara, Turkey
3Department of Molecular Biology and Genetics, University of Koc, Istanbul, Turkey
REF. NO. IJHG-593
PAPER UNDER PROCESSING
Angiotensin-Converting Enzyme Gene Insersion/Deletion Polymorphism in Patients with Pulmonary Thromboembolism
Selma Yeşilkaya1, Mutlu Karkucak2, Hikmet Çoban3*, Ahmet Ursavaş4, Mehmet Türe5 and Tahsin Yakut5
1Department of Pulmonary Medicine, Samsun Hospital for Pulmonary Diseases, Samsun, Turkey
2Department of Medical Genetics, Sakarya University Training and Research Hospital, Sakarya, Turkey
3Department of Pulmonary Medicine, Sakarya University Training and Research Hospital, Sakarya, Turkey
4Department of Pulmonary Medicine, Uludağ University, Medical Faculty, Bursa, Turkey
5Department of Medical Genetics, Uludağ University, Medical Faculty, Bursa, Turkey
REF. NO. IJHG-594
PAPER UNDER PROCESSING
Oxidative DNA Damage, Oxidative Stress and Genetic Susceptibility- Prognostic Scores in ‘Missing’ COPD Cases
Gursatej Gandhi and Gurpreet Kaur*
Department of Human Genetics, Guru Nanak Dev University, Amritsar, India 143001
Address correspondence to
The present status of the paper is available on our website and it has been
categoriSed as follow
PAPER UNDER PROCESSING
1. PAPER For Review
- Paper has been submitted to the Referees for Review
2. PAPER For REVISION
– Acceptable After Substantial Revision. Needs to be re-referred
3. PAPER ACCEPTABLE AFTER REVISION
- Acceptable After Minor Revision or Acceptable After Moderate Revision. No need to referee again
4. PAPER ACCEPTED
-The galley proof of the paper will be sent for final corrections in due course of time
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-When all the formalities have been completed