Indian Journal of Human Genetics
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ORIGINAL COMMUNICATIONS
Genetic damage in mobile phone users: some preliminary findings
Gursatej Gandhi, Anita
[ABSTRACT]  [FULL TEXT]  [PDF] [CITATIONS]
  61,182 412 9
Association of SP-D, MBL and I-NOS genetic variants with pulmonary tuberculosis
Mudit Vaid, Savneet Kaur, Madan Taruna, Hari Singh, Vijay K Gupta, KJR Murthy, Puranam U Sarma
[ABSTRACT]  [FULL TEXT]  [PDF]
  22,458 181 -
Pericentric inversion of chromosome 9[inv(9)(p12q13)]: Its association with genetic diseases
Babu V Rao, Lily Kerketta, Seema Korgaonkar, Kanjaksha Ghosh
[ABSTRACT]  [FULL TEXT]  [PDF] [CITATIONS]
  9,345 512 2
ORIGINAL ARTICLE
Impact of pericentric inversion of Chromosome 9 [inv (9) (p11q12)] on infertility
Hossein Mozdarani, Anahita Mohseni Meybodi, Hamideh Karimi
[ABSTRACT]  [FULL TEXT]  [PDF] [CITATIONS]
  8,189 437 1
REVIEW ARTICLE
Connexin 26 and autosomal recessive non-syndromic hearing loss
Monisha Mukherjee, SR Phadke, Balraj Mittal
[ABSTRACT]  [FULL TEXT]  [PDF]
  7,317 233 -
Contribution of genomics, proteomics, and single-nucleotide polymorphism in toxicology research and Indian scenario
S Patel, D Parmar, YK Gupta, MP Singh
[ABSTRACT]  [FULL TEXT]  [PDF] [CITATIONS]
  7,038 499 2
ORIGINAL ARTICLES
Identification of a rare blood group, "Bombay (Oh) phenotype," in Bhuyan tribe of Northwestern Orissa, India
RS Balgir
[ABSTRACT]  [FULL TEXT]  [PDF]
  6,915 254 -
ORIGINAL COMMUNICATIONS
Prevalence of congenital heart diseases in Mysore
R Smitha, SC Karat, D Narayanappa, B Krishnamurthy, SN Prasanth, NB Ramachandra
[ABSTRACT]  [FULL TEXT]  [PDF] [CITATIONS]
  6,826 254 2
CASE REPORTS
Facio-auricular vertebral syndrome-a case report
M V. V. Reddy, PP Reddy, P Usha Rani, L Hema Bindu
[ABSTRACT]  [FULL TEXT]  [PDF] [CITATIONS]
  6,756 178 2
ORIGINAL ARTICLE
Detection of Y STR markers of male fetal dna in maternal circulation
Seema P Nair, Sam Peter, VV Pillay, UM Remya, R Krishnaprasad, B Rajammal
[ABSTRACT]  [FULL TEXT]  [PDF]
  6,479 242 -
REVIEW ARTICLE
Stem cells: A new paradigm
Sachin Kumar, NP Singh
[ABSTRACT]  [FULL TEXT]  [PDF]
  6,051 582 -
BRIEF REPORT
Chromosome 12;15 rearrangements in patients with recurrent miscarriage
SB Nair, G Mukundan, BM Paul, L Ramachandran, KK Gopinathan, Sajayan Joseph
[ABSTRACT]  [FULL TEXT]  [PDF]
  6,182 258 -
ORIGINAL COMMUNICATIONS
Molecular characterization of mutations causing β -thalassemia in Faisalabad Pakistan using the amplification refractory mutation system (ARMS-PCR)
Shahid M Baig, F Rabbi, U Hameed, JA Qureshi, Z Mahmood, SH Bokhari, A Kiani, H Hassan, JM Baig, A Azhar, T Zaman
[ABSTRACT]  [FULL TEXT]  [PDF] [CITATIONS]
  5,618 374 3
HLA-A allele frequency and haplotype distribution in the dravidian tribal communities of south India
R Thomas, M Banerjee
[ABSTRACT]  [FULL TEXT]  [PDF] [CITATIONS]
  5,578 204 2
REVIEW ARTICLE
An understanding the genetic basis of congenital heart disease
Smitha Ramegowda, Nallur B Ramachandra
[ABSTRACT]  [FULL TEXT]  [PDF]
  5,264 364 -
Past, present and future perspectives of genetic therapy in gliomas
Tobias Alécio Mattei, Ricardo Ramina, Marcos Tatagiba, Paulo Henrique Aguiar
[ABSTRACT]  [FULL TEXT]  [PDF]
  5,434 169 -
Application of diagnostic methods and molecular diagnosis of hemoglobin disorders in Khuzestan province of Iran
Rahim Fakher, Kaeikhaei Bijan, Akbari Mohammad Taghi
[ABSTRACT]  [FULL TEXT]  [PDF] [CITATIONS]
  5,008 588 5
REVIEW ARTICLES
DNA profiling: Social, legal, or biological parentage
AK Sharma
[ABSTRACT]  [FULL TEXT]  [PDF]
  5,150 363 -
BRIEF REPORT
Role of intrauterine Rubella infection in the causation of congenital deafness
MVV Reddy, Hema L Bindu, PP Reddy, Usha P Rani
[ABSTRACT]  [FULL TEXT]  [PDF]
  4,996 160 -
ORIGINAL COMMUNICATIONS
Loss of sex chromosome in acute myeloid leukemia
Sonal R Bakshi, Purvi M Kakadia, Manisha M Brahmbhatt, Pina J Trivedi, Shwetal M Rawal, Samarth S Bhatt, Bharat J Parikh, Kirti M Patel, Shilin N Shukla, Pankaj M Shah
[ABSTRACT]  [FULL TEXT]  [PDF]
  4,931 161 -
REVIEW ARTICLE
Complement receptor 1 and the molecular pathogenesis of malaria
Monika Gandhi
[ABSTRACT]  [FULL TEXT]  [PDF]
  4,693 356 -
SHORT COMMUNICATION
Genetic heterogeneity of population structure in 15 major scheduled tribes in central-eastern India: A study of immuno-hematological disorders
RS Balgir
[ABSTRACT]  [FULL TEXT]  [PDF] [CITATIONS]
  4,801 216 2
ORIGINAL ARTICLES
Possible risk factors for Down syndrome and sex chromosomal aneuploidy in Mysore, South India
Suttur S Malini, Nallur B Ramachandra
[ABSTRACT]  [FULL TEXT]  [PDF]
  4,838 164 -
REVIEW ARTICLE
The impact of consanguinity on the Indian population
AH Bittles
[ABSTRACT]  [FULL TEXT]  [PDF] [CITATIONS]
  4,622 269 6
ORIGINAL COMMUNICATIONS
Menstrual history in women with down syndrome - A review
Priya Ranganath, Sayee Rajangam
[ABSTRACT]  [FULL TEXT]  [PDF]
  4,712 99 -
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