Indian Journal of Human Genetics
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ORIGINAL COMMUNICATIONS
Genetic damage in mobile phone users: some preliminary findings
Gursatej Gandhi, Anita
May-August 2005, 11(2):99-104
DOI:10.4103/0971-6866.16810  
  39 70,962 732
ORIGINAL ARTICLES
Frequency of β-thalassemia trait and other hemoglobinopathies in northern and western India
Nishi Madan, Satendra Sharma, SK Sood, Roshan Colah, HM Bhatia
January-April 2010, 16(1):16-25
DOI:10.4103/0971-6866.64941  PMID:20838487
  29 7,396 485
ORIGINAL COMMUNICATIONS
Prevalence of congenital heart diseases in Mysore
R Smitha, SC Karat, D Narayanappa, B Krishnamurthy, SN Prasanth, NB Ramachandra
January-April 2006, 12(1):11-16
DOI:10.4103/0971-6866.25296  
  17 10,364 434
ORIGINAL ARTICLES
Frequency of fokI and taqI polymorphism of vitamin D receptor gene in Indian population and its association with 25-hydroxyvitamin D levels
Aparna A Bhanushali, Namrata Lajpal, Smita S Kulkarni, Sandeep S Chavan, Sarita S Bagadi, Bibhu R Das
September-December 2009, 15(3):108-113
DOI:10.4103/0971-6866.60186  PMID:21088715
  16 3,821 131
ORIGINAL COMMUNICATIONS
Cytogenetic causes for recurrent spontaneous abortions - An experience of 742 couples (1484 cases)
S Dubey, MR Chowdhury, B Prahlad, V Kumar, R Mathur, S Hamilton, M Kabra, P SN Menon, IC Verma
May-August 2005, 11(2):94-98
DOI:10.4103/0971-6866.16809  
  15 7,270 372
BRIEF REPORT
Congenital malformations at birth in Central India: A rural medical college hospital based data
Amar Taksande, Krishna Vilhekar, Pushpa Chaturvedi, Manish Jain
September-December 2010, 16(3):159-163
DOI:10.4103/0971-6866.73412  PMID:21206705
  13 5,068 161
ORIGINAL ARTICLES
Genetic variation in nucleotide excision repair pathway genes influence prostate and bladder cancer susceptibility in North Indian population
Rama D Mittal, Raju K Mandal
January-April 2012, 18(1):47-55
DOI:10.4103/0971-6866.96648  
  13 2,328 64
ORIGINAL COMMUNICATIONS
Y chromosome microdeletions in Turkish infertile men
Ayse Gul Zamani, Ruhusen Kutlu, H Gul Durakbasi-Dursun, Huseyin Gorkemli, Aynur Acar
May-August 2006, 12(2):66-71
DOI:10.4103/0971-6866.27788  
  13 5,768 271
Pericentric inversion of chromosome 9[inv(9)(p12q13)]: Its association with genetic diseases
Babu V Rao, Lily Kerketta, Seema Korgaonkar, Kanjaksha Ghosh
September-December 2006, 12(3):129-132
DOI:10.4103/0971-6866.29856  
  13 23,763 714
ORIGINAL ARTICLES
MTHFR Gene variants C677T, A1298C and association with Down syndrome: A case-control study from South India
Cyrus Cyril, Padmalatha Rai, N Chandra, PM Gopinath, K Satyamoorthy
May-August 2009, 15(2):60-64
DOI:10.4103/0971-6866.55217  PMID:20680153
  12 4,425 363
Risk conferred by FokI polymorphism of vitamin D receptor (VDR) gene for essential hypertension
N Swapna, U Mohana Vamsi, G Usha, T Padma
September-December 2011, 17(3):201-206
DOI:10.4103/0971-6866.92104  PMID:22345993
  12 3,608 56
REVIEW ARTICLE
The impact of consanguinity on the Indian population
AH Bittles
July-December 2002, 8(2):45-51
  12 8,565 465
ORIGINAL ARTICLES
The CTLA4 -819 C/T and +49 A/G dimorphisms are associated with Type 1 diabetes in Egyptian children
Hatem Mohamed Saleh, Nestor Rohowsky, Michael Leski
September-December 2008, 14(3):92-98
DOI:10.4103/0971-6866.45001  PMID:20300303
  11 3,138 130
Methionine synthase polymorphisms (MTR 2756 A>G and MTR 2758 C>G) frequencies and distribution in the Jordanian population and their correlation with neural tube defects in the population of the northern part of Jordan
Helmi Yousif Al Farra
September-December 2010, 16(3):138-143
DOI:10.4103/0971-6866.73405  PMID:21206701
  11 2,700 69
REVIEW ARTICLE
Application of diagnostic methods and molecular diagnosis of hemoglobin disorders in Khuzestan province of Iran
Rahim Fakher, Kaeikhaei Bijan, Akbari Mohammad Taghi
January-April 2007, 13(1):5-15
DOI:10.4103/0971-6866.32028  PMID:21957335
  11 9,003 763
REVIEW ARTICLES
Challenges and recommendations for conducting epidemiological studies in the field of epilepsy pharmacogenetics
Sandeep Grover, Meenal Gupta, Ritushree Kukreti
May 2011, 17(4):4-11
DOI:10.4103/0971-6866.80351  PMID:21747586
  11 2,334 95
DR. SANDHYA GHOSH MEMORIAL ORATION
The case for dedicated sickle cell centres
Graham R Serjeant
September-December 2006, 12(3):148-151
DOI:10.4103/0971-6866.29861  
  10 5,688 190
ORIGINAL ARTICLE
Impact of pericentric inversion of Chromosome 9 [inv (9) (p11q12)] on infertility
Hossein Mozdarani, Anahita Mohseni Meybodi, Hamideh Karimi
January-April 2007, 13(1):26-29
DOI:10.4103/0971-6866.32031  PMID:21957338
  10 17,810 564
ORIGINAL ARTICLES
Frequency of twinning in southwest Nigeria
A Akinboro, MA Azeez, AA Bakare
May-August 2008, 14(2):41-47
DOI:10.4103/0971-6866.44104  PMID:20300293
  10 3,732 146
Allelic variants of DYX1C1 are not associated with dyslexia in India
Pushpa Saviour, Satish Kumar, U Kiran, Rajasekhara Reddy Ravuri, VR Rao, Nallur Basappa Ramachandra
September-December 2008, 14(3):99-102
DOI:10.4103/0971-6866.45002  PMID:20300304
  10 2,632 156
Large-scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,797 individuals
Khalil Hamzi, Amal Tazzite, Sellama Nadifi
September-December 2011, 17(3):212-217
DOI:10.4103/0971-6866.92105  PMID:22345995
  10 2,550 80
SHORT ARTICLE
Physical growth of children with sickle cell disease
Malay B Mukherjee, RR Gangakhedkar
July-December 2004, 10(2):70-72
  10 6,652 214
ORIGINAL ARTICLES
Can novel Apo A-I polymorphisms be responsible for low HDL in South Asian immigrants?
Sunita Dodani, Yanbin Dong, Haidong Zhu, Varghese George
January-April 2008, 14(1):9-15
DOI:10.4103/0971-6866.42321  PMID:20300285
  9 5,827 215
Apolipoprotein E gene polymorphism and dyslipidaemia in adult Asian Indians: A population based study from calcutta, India
Mithun Das, Susil Pal, Arnab Ghosh
September-December 2008, 14(3):87-91
DOI:10.4103/0971-6866.45000  PMID:20300302
  9 3,232 218
Association of polymorphisms in leptin receptor gene with obesity and type 2 diabetes in the local population of Coimbatore
Devi Murugesan, Thirunavukkarasu Arunachalam, Viraragavan Ramamurthy, Selvi Subramanian
May-August 2010, 16(2):72-77
DOI:10.4103/0971-6866.69350  PMID:21031055
  8 4,079 216
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