(Q36245306)

13 August 2017

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title

The Indian Genome Variation database (IGVdb): a project overview (English)

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Indian Genome Variation Consortium

13 August 2017

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series ordinal

1

object named as

Indian Genome Variation Consortium

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13 August 2017

language of work or name

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25 August 2005

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13 August 2017

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13 August 2017

volume

118

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13 August 2017

issue

1

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13 August 2017

page(s)

1-11

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CAG repeat instability at SCA2 locus: anchoring CAA interruptions and linked single nucleotide polymorphisms

13 August 2017

cites work

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12 December 2020

MLC1 gene is associated with schizophrenia and bipolar disorder in Southern India

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12 December 2020

CCR5 Delta32 deletion and atopic asthma in India.

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12 December 2020

Mitochondrial DNA variation in ranked caste groups of Maharashtra (India) and its implication on genetic relationships and origins

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12 December 2020

Genomic structures and population histories of linguistically distinct tribal groups of India

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12 December 2020

CYP11B2 gene polymorphisms and hypertension in highlanders accustomed to high salt intake.

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12 December 2020

JSNP: a database of common gene variations in the Japanese population

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12 December 2020

Human-specific insertion/deletion polymorphisms in Indian populations and their possible evolutionary implications

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12 December 2020

Haplotyping in pedigrees via a genetic algorithm.

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12 December 2020

Molecular pathology of haemophilia B: identification of five novel mutations including a LINE 1 insertion in Indian patients.

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12 December 2020

Association of IL4 gene polymorphisms with asthma in North Indians

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12 December 2020

Identification of polymorphic motifs using probabilistic search algorithms

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12 December 2020

Molecular characterization of hemophilia B in North Indian families: identification of novel and recurrent molecular events in the factor IX gene.

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12 December 2020

Demographic history of India and mtDNA-sequence diversity.

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12 December 2020

The costs of human inbreeding and their implications for variations at the DNA level

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12 December 2020

Founder haplotype for Machado-Joseph disease in the Indian population: novel insights from history and polymorphism studies

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12 December 2020

dbSNP: the NCBI database of genetic variation

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12 December 2020

Ethnic India: A Genomic View, With Special Reference to Peopling and Structure

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12 December 2020

eNOS allelic variants at the same locus associate with HAPE and adaptation.

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12 December 2020

The genetic heritage of the earliest settlers persists both in Indian tribal and caste populations

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12 December 2020

Y-chromosome and mitochondrial DNA polymorphisms in Indian populations

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12 December 2020

Association of IFNG gene polymorphism with asthma in the Indian population

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12 December 2020

Prehistoric human colonization of India

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12 December 2020

Endogamy, consanguinity and community genetics

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12 December 2020

High-resolution analysis of Y-chromosomal polymorphisms reveals signatures of population movements from Central Asia and West Asia into India

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12 December 2020

Study of the single nucleotide polymorphism (SNP) at the palindromic sequence of hypersensitive site (HS)4 of the human beta-globin locus control region (LCR) in Indian population

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12 December 2020

Genetic evidence on the origins of Indian caste populations

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12 December 2020

A nonsense mutation in the synaptogyrin 1 gene in a family with schizophrenia

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12 December 2020

Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation

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12 December 2020

Negligible male gene flow across ethnic boundaries in India, revealed by analysis of Y-chromosomal DNA polymorphisms

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12 December 2020

Signal transducer and activator of transcription 6 haplotypes and asthma in the Indian population

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12 December 2020

Expanding colonies and expanding repeats

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12 December 2020

Association of an intragenic microsatellite marker in the CC16 gene with asthma in the Indian population

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12 December 2020

Y-chromosome SNP haplotypes suggest evidence of gene flow among caste, tribe, and the migrant Siddi populations of Andhra Pradesh, South India

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12 December 2020

Molecular analysis of Huntington's disease and linked polymorphisms in the Indian population.

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12 December 2020

CAG repeat expansion in the androgen receptor gene is not associated with male infertility in Indian populations.

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12 December 2020

Apolipoprotein E and presenilin-1 allelic variation and Alzheimer's disease in India.

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12 December 2020

HGVbase: a curated resource describing human DNA variation and phenotype relationships

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12 December 2020

DNA sequence variation and haplotype structure of the ICAM1 and TNF genes in 12 ethnic groups of India reveal patterns of importance in designing association studies

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12 December 2020

Variations in angiotensin-converting enzyme gene insertion/deletion polymorphism in Indian populations of different ethnic origins

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12 December 2020

Ethnic populations of India as seen from an evolutionary perspective

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12 December 2020

Genetic clues to dispersal in human populations: retracing the past from the present

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12 December 2020

Ethnic differences in distributions of GSTM1 and GSTT1 homozygous "null" genotypes in India

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12 December 2020

The Celera Discovery System.

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12 December 2020

Analysis of CAG and CCG repeats in Huntingtin gene among HD patients and normal populations of India

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12 December 2020

Evidence of a common founder for SCA12 in the Indian population.

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12 December 2020

Identification of single-nucleotide and repeat polymorphisms in two candidate genes, interleukin 4 receptor (IL4RA) and signal transducer and activator of transcription protein 6 (STAT6), for Th2-mediated diseases

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12 December 2020

The International HapMap Project

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12 December 2020

Sickle cell gene haplotypes in Relli and Thurpu Kapu populations of Andhra Pradesh

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12 December 2020

A_16_C haplotype in the FcepsilonRIbeta gene confers a higher risk for atopic asthma in the Indian population

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12 December 2020

Female gene flow stratifies Hindu castes

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12 December 2020

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12 December 2020

10.1007/S00439-005-0009-9

Identifiers

DOI

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13 August 2017

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