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Chromatin is a Dynamic Structure

Resonance, 2022-06, Vol.27 (6), p.983-1002

Raman, Rajiva

2022

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What Makes an Individual a Male or a Female?

Resonance, 2020-02, Vol.25 (2), p.233-247

Raman, Rajiva

2020

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TGFβ3, MSX1, and MMP3 as Candidates for NSCL±P in an Indian Population

The Cleft palate-craniofacial journal, 2019-03, Vol.56 (3), p.363-372

2019

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Low birthweight (LBW) and neonatal hyperbilirubinemia (NNH) in an Indian cohort: association of homocysteine, its metabolic pathway genes and micronutrients as risk factors

PloS one, 2013-08, Vol.8 (8), p.e71587-e71587

2013

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Meiotic Cell Division–Why and How?: A Genetic Perspective

Resonance, 2023-06, Vol.28 (6), p.859-876

Raman, Rajiva

2023

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Meiotic Cell Division–Why and How?

Resonance, 2023-01, Vol.28 (6), p.859-876

Raman Rajiva

2023

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Heme oxygenase-1 gene variants and hyperbilirubinemia risk in North Indian newborns

European journal of pediatrics, 2013-12, Vol.172 (12), p.1627-1632

2013

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Dosage Compensation: A Mechanism to Equalize X-linked Gene Products Between the Sexes

Resonance, 2021-05, Vol.26 (5), p.649-669

Raman, Rajiva

2021

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Dosage Compensation

Resonance, 2021-01, Vol.26 (5), p.649-669

Raman Rajiva

2021

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Hereditary prosopagnosia (HPA): the first report outside the Caucasian population

Journal of human genetics, 2007-03, Vol.52 (3), p.230-236

2007

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SPECIAL SECTION: Dosage compensation, epigenetic mechanisms, and mapping disease loci: Foreword

Journal of genetics, 2018-06, Vol.97 (2), p.355-356

2018

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Correction: Low Birthweight (LBW) and Neonatal Hyperbilirubinemia (NNH) in an Indian Cohort: Association of Homocysteine, Its Metabolic Pathway Genes and Micronutrients as Risk Factors

PloS one, 2013-09, Vol.8 (9)

2013

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MTHFR C677T and A1298C polymorphisms are risk factors for Down's syndrome in Indian mothers

Journal of human genetics, 2006-04, Vol.51 (4), p.278-283

2006

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A novel non-coding RNA within an intron of CDH2 and association of its SNP with non-syndromic cleft lip and palate

Gene, 2018-06, Vol.658, p.123-128

2018

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Nutritional Modulation of Gene Function in Disease Susceptibility: Homocysteine-Folate Metabolism Pathway

Proceedings of the Indian National Science Academy, Part A: Physical sciences, 2016-12, Vol.82

Raman, Rajiva

2016

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In Remembrance: Mary Frances Lyon

Journal of genetics, 2015-12, Vol.94 (4), p.559-562

Raman, Rajiva

2015

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Molecular diagnosis of 46,XY DSD and identification of a novel 8 nucleotide deletion in exon 1 of the SRD5A2 gene

Journal of Pediatric Endocrinology and Metabolism, 2010-04, Vol.23 (4), p.379-385

2010

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Diversity of sickle cell trait in Jharkhand state in India: Is it the zone of contact between two geographically and ethnically distinct populations in India?

Journal of biosciences, 2015-09, Vol.40 (3), p.539-547

2015

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A386G polymorphism of the DAZL gene is not associated with idiopathic male infertility in North India

Journal of human reproductive sciences, 2009-07, Vol.2 (2), p.54-56

2009

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Conservation of Ovary-Specific Genes, Foxl2, Aromatase, and Rspo1, in the Common Indian Garden Lizard, Calotes versicolor, That Lacks Chromosomal or Temperature-Dependent Sex Determination

Sexual development, 2018-01, Vol.12 (6), p.295-307

2018

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Genotype–phenotype correlation and report of novel mutations in β-globin gene in thalassemia patients

Blood cells, molecules, & diseases, 2015-06, Vol.55 (1), p.10-14

2015

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Use of Animals in Scientific Research and Education

Proceedings of the Indian National Science Academy, Part A: Physical sciences, 2014-06, Vol.80 (2), p.497

Raman, Rajiva

2014

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Haemoglobinopathies in eastern Indian states: a demographic evaluation

Journal of community genetics, 2015-01, Vol.6 (1), p.1-8

2015

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Unmethylated/hypomethylated status of developmentally important genes in brain tissue of mammals

South Asian journal of experimental biology, 2015-01, Vol.4 (5), p.226-231

2015

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Heme oxygenase-1 gene variants and hyperbilirubinemia risk in North Indian newborns

European journal of pediatrics, 2013-12, Vol.172 (12), p.1627-1632

2013

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Chromatin is a Dynamic Structure

What Makes an Individual a Male or a Female?

TGFβ3, MSX1, and MMP3 as Candidates for NSCL±P in an Indian Population

Low birthweight (LBW) and neonatal hyperbilirubinemia (NNH) in an Indian cohort: association of homocysteine, its metabolic pathway genes and micronutrients as risk factors

Meiotic Cell Division–Why and How?: A Genetic Perspective

Meiotic Cell Division–Why and How?

Heme oxygenase-1 gene variants and hyperbilirubinemia risk in North Indian newborns

Dosage Compensation: A Mechanism to Equalize X-linked Gene Products Between the Sexes

Dosage Compensation

Hereditary prosopagnosia (HPA): the first report outside the Caucasian population

SPECIAL SECTION: Dosage compensation, epigenetic mechanisms, and mapping disease loci: Foreword

Correction: Low Birthweight (LBW) and Neonatal Hyperbilirubinemia (NNH) in an Indian Cohort: Association of Homocysteine, Its Metabolic Pathway Genes and Micronutrients as Risk Factors

MTHFR C677T and A1298C polymorphisms are risk factors for Down's syndrome in Indian mothers

A novel non-coding RNA within an intron of CDH2 and association of its SNP with non-syndromic cleft lip and palate

Nutritional Modulation of Gene Function in Disease Susceptibility: Homocysteine-Folate Metabolism Pathway

In Remembrance: Mary Frances Lyon

Molecular diagnosis of 46,XY DSD and identification of a novel 8 nucleotide deletion in exon 1 of the SRD5A2 gene

Diversity of sickle cell trait in Jharkhand state in India: Is it the zone of contact between two geographically and ethnically distinct populations in India?

A386G polymorphism of the DAZL gene is not associated with idiopathic male infertility in North India

Conservation of Ovary-Specific Genes, Foxl2, Aromatase, and Rspo1, in the Common Indian Garden Lizard, Calotes versicolor, That Lacks Chromosomal or Temperature-Dependent Sex Determination

Genotype–phenotype correlation and report of novel mutations in β-globin gene in thalassemia patients

Use of Animals in Scientific Research and Education

Haemoglobinopathies in eastern Indian states: a demographic evaluation

Unmethylated/hypomethylated status of developmentally important genes in brain tissue of mammals

Heme oxygenase-1 gene variants and hyperbilirubinemia risk in North Indian newborns

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