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Novel Glioblastoma Markers with Diagnostic and Prognostic Value Identified through Transcriptome Analysis

Clinical cancer research, 2008-05, Vol.14 (10), p.2978-2987

2008

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Inadequate Pre-conception Counseling is a Major Challenge for Antenatal Management of β-Thalassemia: Experience from a Referral Centre in India

Indian journal of hematology & blood transfusion, 2020-04, Vol.36 (2), p.414-416

2020

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Upregulation of ASCL1 and inhibition of Notch signaling pathway characterize progressive astrocytoma

Oncogene, 2005-10, Vol.24 (47), p.7073-7083

2005

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Pre- and Postnatal Analysis of Chromosome 1q44 Deletion in Agenesis of Corpus Callosum

Molecular syndromology, 2015-10, Vol.6 (4), p.187-192

2015

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Generation of Induced Pluripotent Stem Cells from Turner Syndrome (45XO) Fetal Cells for Downstream Modelling of Neurological Deficits Associated with the Syndrome

Journal of visualized experiments, 2021-12 (178)

2021

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Shift in AP-2α localization characterizes astrocytoma progression

Cancer biology & therapy, 2007-03, Vol.6 (3), p.413-418

2007

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Freeman-Sheldon syndrome-prenatal and postnatal diagnosis

Indian journal of pediatrics, 2010-02, Vol.77 (2), p.196-197

2010

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Culturing Human Tumor Cells: One Source for All

Cancer Biology & Therapy, 2003-11, Vol.2 (6), p.725-726

2003

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Exonic microdeletions in the X-linked PQBP1 gene in mentally retarded patients : a pathogenic mutation and in-frame deletions of uncertain effect

European journal of human genetics : EJHG, 2006-04, Vol.14 (4), p.418-425

2006

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Pre- and Postnatal Diagnosis of 10p14 Deletion and 22q11.2 Deletion Syndrome and Significance of Non-Cardiac Markers

Cytogenetic and genome research, 2016-01, Vol.148 (4), p.249-255

2016

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A Homozygous Missense Variant in INPP5E Associated with Joubert Syndrome and Related Disorders

Molecular syndromology, 2017-11, Vol.8 (6), p.313-317

2017

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Pre- and Postnatal Analysis of Chromosome 15q26.1 and 8p23.1 Deletions in Congenital Diaphragmatic Hernia

Molecular syndromology, 2016-02, Vol.6 (5), p.248-253

2016

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Pre- and Postnatal Diagnosis of 5q35.1 and 8p23.1 Deletion in Congenital Heart Disease

Indian journal of pediatrics, 2016-11, Vol.83 (12-13), p.1484-1485

2016

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The A1298C Methylenetetrahydrofolate Reductase Gene Variant as a Susceptibility Gene for Non-Syndromic Conotruncal Heart Defects in an Indian Population

Pediatric cardiology, 2015-10, Vol.36 (7), p.1470-1475

2015

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Effects of an Integrated Yoga Program in Modulating Psychological Stress and Radiation-Induced Genotoxic Stress in Breast Cancer Patients Undergoing Radiotherapy

Integrative cancer therapies, 2007-09, Vol.6 (3), p.242-250

2007

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A novel de novo heterozygous deletion at 13q14.2-q21.1 in two siblings with mild intellectual disability

Gene reports, 2018-09, Vol.12, p.201-207

2018

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Sporadic spinocerebellar ataxia, type 5: First report from India

Neurology India, 2018-01, Vol.66 (1), p.230-231

2018

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Differential protein expression in human gliomas and molecular insights

Proteomics (Weinheim), 2005-03, Vol.5 (4), p.1167-1177

2005

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Single Nucleotide Polymorphism-Based Noninvasive Prenatal Testing: Experience in India

Journal of obstetrics and gynaecology of India, 2018-12, Vol.68 (6), p.462-470

2018

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Squared nasal root, nasal voice -indicators of 22 q11.2 deletion in patients with psychiatric illness

Molecular cytogenetics, 2014-01, Vol.7 (Suppl 1), p.P76-P76

2014

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Analysis of telomere damage by fluorescence in situ hybridisation on micronuclei in lymphocytes of breast carcinoma patients after radiotherapy

Breast cancer research and treatment, 2008-01, Vol.107 (1), p.25-31

2008

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Shift in AP-2alpha localization characterizes astrocytoma progression

Cancer biology & therapy, 2007-03, Vol.6 (3), p.413-418

2007

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Evaluation of Cardiac Defect in a Fetus with 8p Interstitial Deletion

International journal of human genetics, 2010-03, Vol.10 (1-3), p.183-186

2010

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Differential protein expression in human gliomas and molecular insights

Proteomics (Weinheim), 2005-07, Vol.5 (10), p.2702-2702

2005

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Alterations in tumour suppressor gene p53 in human gliomas from Indian patients

Journal of biosciences, 2002-12, Vol.27 (7), p.673-678

2002

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Novel Glioblastoma Markers with Diagnostic and Prognostic Value Identified through Transcriptome Analysis

Inadequate Pre-conception Counseling is a Major Challenge for Antenatal Management of β-Thalassemia: Experience from a Referral Centre in India

Upregulation of ASCL1 and inhibition of Notch signaling pathway characterize progressive astrocytoma

Pre- and Postnatal Analysis of Chromosome 1q44 Deletion in Agenesis of Corpus Callosum

Generation of Induced Pluripotent Stem Cells from Turner Syndrome (45XO) Fetal Cells for Downstream Modelling of Neurological Deficits Associated with the Syndrome

Shift in AP-2α localization characterizes astrocytoma progression

Freeman-Sheldon syndrome-prenatal and postnatal diagnosis

Culturing Human Tumor Cells: One Source for All

Exonic microdeletions in the X-linked PQBP1 gene in mentally retarded patients : a pathogenic mutation and in-frame deletions of uncertain effect

Pre- and Postnatal Diagnosis of 10p14 Deletion and 22q11.2 Deletion Syndrome and Significance of Non-Cardiac Markers

A Homozygous Missense Variant in INPP5E Associated with Joubert Syndrome and Related Disorders

Pre- and Postnatal Analysis of Chromosome 15q26.1 and 8p23.1 Deletions in Congenital Diaphragmatic Hernia

Pre- and Postnatal Diagnosis of 5q35.1 and 8p23.1 Deletion in Congenital Heart Disease

The A1298C Methylenetetrahydrofolate Reductase Gene Variant as a Susceptibility Gene for Non-Syndromic Conotruncal Heart Defects in an Indian Population

Effects of an Integrated Yoga Program in Modulating Psychological Stress and Radiation-Induced Genotoxic Stress in Breast Cancer Patients Undergoing Radiotherapy

A novel de novo heterozygous deletion at 13q14.2-q21.1 in two siblings with mild intellectual disability

Sporadic spinocerebellar ataxia, type 5: First report from India

Differential protein expression in human gliomas and molecular insights

Single Nucleotide Polymorphism-Based Noninvasive Prenatal Testing: Experience in India

Squared nasal root, nasal voice -indicators of 22 q11.2 deletion in patients with psychiatric illness

Analysis of telomere damage by fluorescence in situ hybridisation on micronuclei in lymphocytes of breast carcinoma patients after radiotherapy

Shift in AP-2alpha localization characterizes astrocytoma progression

Evaluation of Cardiac Defect in a Fetus with 8p Interstitial Deletion

Differential protein expression in human gliomas and molecular insights

Alterations in tumour suppressor gene p53 in human gliomas from Indian patients

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