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The Neural Basis of Social Cognition in Typically Developing Children and Its Relationship to Social Functioning

Frontiers in psychology, 2021-12, Vol.12, p.714176-714176

2021

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G372(P) Can we do more to prevent picu admissions for children presenting with severe asthma? what are the modifiable factors

Archives of disease in childhood, 2019-05, Vol.104 (Suppl 2), p.A151

2019

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Novel mutations in typical and atypical genetic loci through exome sequencing in autosomal recessive cerebellar ataxia families

Clinical genetics, 2014-10, Vol.86 (4), p.335-341

2014

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ICTs and Development: A Study of Telecentres in Rural India

Mukerji, M

1, 2013

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Diverse facets of COMT: from a plausible predictive marker to a potential drug target for schizophrenia

Current molecular medicine, 2011-12, Vol.11 (9), p.732-743

2011

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Spinocerebellar ataxia 7 (sca7) in India: Genotype–/INS;phenotype correlation and insight into origin of mutation in a predisposed endogamous population

Journal of the neurological sciences, 2013-10, Vol.333, p.e107-e107

2013

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Genetic deconvolution of cerebellar ataxias in India through next generation sequencing: Novel mutations in atypical and typical genetic loci

Journal of the neurological sciences, 2013-10, Vol.333, p.e142-e142

2013

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Reduced penetrance alleles of TBP (SCA17) in Indian ataxia cohort: Homozygous mutation and ambiguity of 41–/INS;44 CAG/CAA for pathogenic association

Journal of the neurological sciences, 2013-10, Vol.333, p.e69-e69

2013

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3.080 MITOCHONDRIAL D-LOOP HOMOPLASMIC T16519C POINT MUTATION AND IDENTIFICATION OF NOVEL MARKERS ASSOCIATED WITH FRDA PATIENTS IN INDIAN POPULATION

Parkinsonism & related disorders, 2012, Vol.18, p.S189-S189

2012

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

Human genetics, 2000-02, Vol.106 (2), p.179-187

2000

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Evidence of a Common Founder for SCA12 in the Indian Population

Annals of human genetics, 2005-09, Vol.69 (5), p.528-534

2005

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Mobilités d’ingénieurs en Europe, XVe-XVIIIe siècle: Mélanges en l’honneur d’Hélène Vérin

2017

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Genome-wide prediction of G4 DNA as regulatory motifs: role in Escherichia coli global regulation

Genome Research, 2006-05, Vol.16 (5), p.644-655

2006

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Genomic insights into ayurvedic and western approaches to personalized medicine

Journal of genetics, 2016-03, Vol.95 (1), p.209-228

2016

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P3.043 FRDA mutation predates divergence of European and Indian populations of Indo-European origin?

Parkinsonism & related disorders, 2009, Vol.15, p.S159-S159

2009

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From 'JUNK' to Just Unexplored Noncoding Knowledge: the case of transcribed Alus

Briefings in functional genomics, 2011-09, Vol.10 (5), p.294-311

2011

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EGLN1 involvement in high-altitude adaptation revealed through genetic analysis of extreme constitution types defined in Ayurveda

Proceedings of the National Academy of Sciences - PNAS, 2010-11, Vol.107 (44), p.18961-18966

2010

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Alu repeat analysis in the complete human genome: trends and variations with respect to genomic composition

Bioinformatics, 2004-04, Vol.20 (6), p.813-817

2004

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The Effects of Potassium Channel Blockers on Progesterone-Induced Suppression of Rat Portal Vein Contractility

Journal of pharmacy and pharmacology, 2000-08, Vol.52 (8), p.983-990

2000

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The Effect of Progesterone on Spontaneous and Agonist-Evoked Contractions of the Rat Aorta and Portal Vein

Journal of pharmacy and pharmacology, 2000-07, Vol.52 (7), p.843-849

2000

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From 'JUNK' to Just Unexplored Noncoding Knowledge: the case of transcribed Alus

Briefings in functional genomics, 2011-11, Vol.10 (6), p.400-400

2011

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Molecular analysis of Friedreich's ataxia locus in the Indian population

Acta neurologica Scandinavica, 2000-10, Vol.102 (4), p.227-229

2000

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G26 Social media support for parents and young people with food allergy – an analysis of facebook content

Archives of disease in childhood, 2016-04, Vol.101 (Suppl 1), p.A19-A19

2016

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

Human molecular genetics, 2001-10, Vol.10 (21), p.2437-2446

2001

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High Incidence of Postoperative Nausea and Vomiting in Transgender Women Undergoing Facial Feminization Procedures

Plastic and reconstructive surgery. Global open, 2023-11, Vol.11 (11), p.e5360-e5360

2023

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The Neural Basis of Social Cognition in Typically Developing Children and Its Relationship to Social Functioning

G372(P) Can we do more to prevent picu admissions for children presenting with severe asthma? what are the modifiable factors

Novel mutations in typical and atypical genetic loci through exome sequencing in autosomal recessive cerebellar ataxia families

ICTs and Development: A Study of Telecentres in Rural India

Diverse facets of COMT: from a plausible predictive marker to a potential drug target for schizophrenia

Spinocerebellar ataxia 7 (sca7) in India: Genotype–/INS;phenotype correlation and insight into origin of mutation in a predisposed endogamous population

Genetic deconvolution of cerebellar ataxias in India through next generation sequencing: Novel mutations in atypical and typical genetic loci

Reduced penetrance alleles of TBP (SCA17) in Indian ataxia cohort: Homozygous mutation and ambiguity of 41–/INS;44 CAG/CAA for pathogenic association

3.080 MITOCHONDRIAL D-LOOP HOMOPLASMIC T16519C POINT MUTATION AND IDENTIFICATION OF NOVEL MARKERS ASSOCIATED WITH FRDA PATIENTS IN INDIAN POPULATION

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

Evidence of a Common Founder for SCA12 in the Indian Population

Mobilités d’ingénieurs en Europe, XVe-XVIIIe siècle: Mélanges en l’honneur d’Hélène Vérin

Genome-wide prediction of G4 DNA as regulatory motifs: role in Escherichia coli global regulation

Genomic insights into ayurvedic and western approaches to personalized medicine

P3.043 FRDA mutation predates divergence of European and Indian populations of Indo-European origin?

From 'JUNK' to Just Unexplored Noncoding Knowledge: the case of transcribed Alus

EGLN1 involvement in high-altitude adaptation revealed through genetic analysis of extreme constitution types defined in Ayurveda

Alu repeat analysis in the complete human genome: trends and variations with respect to genomic composition

The Effects of Potassium Channel Blockers on Progesterone-Induced Suppression of Rat Portal Vein Contractility

The Effect of Progesterone on Spontaneous and Agonist-Evoked Contractions of the Rat Aorta and Portal Vein

From 'JUNK' to Just Unexplored Noncoding Knowledge: the case of transcribed Alus

Molecular analysis of Friedreich's ataxia locus in the Indian population

G26 Social media support for parents and young people with food allergy – an analysis of facebook content

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

High Incidence of Postoperative Nausea and Vomiting in Transgender Women Undergoing Facial Feminization Procedures

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