Author ID-Abstract ID

Abstract Title

Presenting Author Full Name

253-262

Genetic Screening in optimizing assisted reproductive technologies (ART) Outcomes in cases of Male Infertility and Recurrent Pregnancy Loss- A case series

Preethi Sundar

481-261

Investigating the genetics of Non-Syndromic Tetralogy of Fallot: Insights from WES and in silico analysis of NOTCH1 variants

Prachi Sandeep Oza

483-260

“Understanding Taste Receptor Polymorphism in Indian Population”

Shivangi Sharma

355-259

Polysomy of CEP8 Correlates with Tumor Mitotic Activity in Breast Carcinoma: Analysis of 45 FFPE Sample

Naga Jyothi

476-258

Alterations of gut-immune axis in Guillain Barre Syndrome: A metagenomic study

Sandipan Mondal

478-257

Impact of genetic and epigenetic changes within MAPT gene on the risk of Progressive supranuclear palsy (PSP)

Ravichandiran Kumar

479-256

An Integrated Analysis of Genetic Alterations in Breast Cancer Signaling Pathways

Gowrang Kasaba Manjunath

475-255

Origin, Evolution, and Pathophysiological Diversifications of Vertebrate α1-antitrypsin-like Serpins

Mangesh Rajguru

463-253

"Complex Chromosomal Abnormalities: A Single Case with Balanced Translocation, Mosaicism, and Ring Chromosome

Vidhi Sambhvani

474-252

Possible reasons and outcomes associated with no-call results on Non-invasive Prenatal Screening

Angela Devanboo

473-251

Transformation of Quality of Life of Alzheimer’s disease Cases by Yoga Therapy

Meenakshi Kaushik

466-249

Epistatic interactions of MAPT, STX6, MOBP, and EIF2AK3 genes in Progressive Supranuclear Palsy: New genetic perspectives in the Asian Indian population

Sivapriya Senthilkumar

465-246

Impact of gene-gene interaction of IFN-γ/ IL12 immune-axis in Progressive Supranuclear Palsy (PSP)

Priyanka Kammar D

461-244

Gene-FCCSS: A ressource for investigating genetic factors predisposing to iatrogenic pathologies in childhood cancer survivors

Florent De Vathaire

453-243

VEGFA Polymorphisms in the Pathogenesis of Diabetic Retinopathy: A Systematic Review and Meta-Analysis

Anjana B

458-242

X-Linked Leigh’s Disease in Siblings with PDH Complex Deficiency: A Case Report

Sahil Mathur

457-241

Interphase Chromosome Profiling (ICP), A Novel cytogenetic technique

Soumya Thomas

456-240

Structural and Functional modification of Long Noncoding RNAs induced by Single Nucleotide Polymorphism

Mandakini Singh

452-239

Clinico-genetic profile of inborn errors of cobalamin metabolism: a series of 11 cases from a tertiary care hospital

Aradhya Sekhar Bagchi

431-238

Dietary Interventions in Classical Phenylketonuria with an indigenously manufactured metabolic diet.

Monisha Morris

448-237

BMAL1 Underexpression and Sleep disturbances in Autism Spectrum Disorder: Exploring Circadian and Biological correlates

Madisetty Jayarama Krishna

450-236

A meta approach to predicting the impact of missense of mutations and case studies of mucopolysaccharidosis (MPS)

Aman Vishwakarma

254-235

A Case study of HLA DQ gene mutation in relation to Celiac Disease

Priyadharshini Krishnan

141-234

Exploring the DNA methylation Profile associated with Bardet-Biedl Syndrome: An EPIC array-based approach

J Syed Ali Fathima Afrin

433-233

Prevalence of Chromosomal abnormality of couples with Primary Infertility.

Sarasu J

442-232

Characterizing the impact Runs of Homozygosity on psychiatric disorder risk in Indian population using Whole-Exome Sequencing(WES)

Swathy Prathapan

446-231

USE OF PRIMED IN-SITU LABELLING (PRINS) AS A MOLECULAR CYTOGENETIC TECHNIQUE IN GENOME RESEARCH AND MOLECULAR DIAGNOSTICS

Pooja Kulshreshtha

447-230

Recurrent pregnancy loss

Priyanka A

445-229

Recurrent pregnancy loss

S Arun Kumar

444-228

mBand FISH in characterizing derivative X - Chromosome in 2 patients with Turner Syndrome

Hari Krupa Devi Alagarsamy Govindaraj

443-227

Generation of Long-Lived Lymphoblastoid Cell Lines from Patients with Chromosomal Abnormalities Using Epstein - Barr virus

Krishnamoorthy R

441-226

Hereditary spastic paraplegia due to hyperhomocysteinemia: A potentially modifiable genetic disorder !

Pokala Akhil

440-225

MAX-Mediated Transcriptional Regulation of Pseudouridine(Ѱ) Modified RNAs and Interacting RNA-Binding Proteins: Implications in Cancer Regulatory Networks

Sushree Lipsa Lopamudra Dwibedy

439-224

Achondroplasia and related Disorders

Ambika Srikanth

430-223

Androgen Insensitivity Syndrome (AIS)

Tejashwini Vittal Kumar

436-221

Unravelling Early-Onset Polycystic Kidney Disease: The Role of Bi-Allelic PKD1 Variants in Atypical Presentations

Darshini Mutukumar

435-220

Rare variant in the NID1 gene causing Occipital encephalocele: Case report

Sandhya Nair

73-219

Functional annotations of transcriptomic heterogeneity in ischemic stroke: Evidence from bioinformatic meta-analyses

Debprasad Dutta

376-218

Exploring the Phenotypic spectrum in Prader Willi Syndrome patients along with genotypic analysis.

Sacheta Kulkarni

428-217

DIAGNOSTIC EFFICACY OF NEXT GENERATION SEQUENCING IN PEDIATRIC NEUROLOGICAL DISORDERS

Nagaraj A R

111-216

Uncovering Genetic Mutations in Male Infertility: Insights from Whole Exome Sequencing

Suruthi Abirami B

64-215

Prevention and treatment strategies using preimplantation genetic testing (PGT) for thalassemia and other hematological disorders: A Jaslok Hospital experience.

Sona B. Nair

407-214

Taste Sensitivity and Obesity Risk in Indian Adults: The Impact of Genetic Variations in Sweet and Fat Taste Receptors

Vinithra Ponnusamy

423-213

Title: A study on analyzing the DNA methylation patterns, its roles in Down syndrome and congenital heart disease- A REVIEW ARTICLE

Syamly S

248-212

Prevalence of deleterious Common and Rare variants in Autism-associated genes in Indian cohort of Autism Spectrum Disorders

Meghana K R

50-211

Identification of potential risk genes in congenital heart disease through whole exome sequencing

Chaithra S

263-210

Genetic Insights into Epidermolysis Bullosa: A Cohort Study Highlighting COL7A1, LAMA3, and LAMB3 Mutations

Vaishnavi Parameswaran

419-209

TLR4 Pathway Hyperactivation in Chronic Suppurative Otitis Media: A Potential Therapeutic Target

Dr Jagadisha T V

349-208

Biallelic Variants in CCN2 Underlie an Autosomal Recessive Kyphomelic Dysplasia

Swati Singh

410-207

SEC23B Dysfunction in Congenital Dyserythropoietic Anemia Type II: Insights from Molecular and Gene Expression Studies

Arati Saptarshi

240-206

Clinical and genetic profile of patients with Niemann Pick disease

Nitin Agrawal

259-205

Making Informed Choices: The Role of Preventive Genetics in Reproductive Planning- A case study of Preimplantation Genetic Testing for Monogenic disorders (PGT-M)

Sharanya Kamaraju

402-204

Whole Exome Sequencing for Fetal Structural Anomalies: Expanding the Diagnostic Yield in Prenatal Care Royal hospital experiences

Nadia Alhashmi

377-203

Genetic variants in bilateral cleft lip and cleft palate

Inusha Panigrahi

397-201

The Impact of Aging on Synaptic Redox Homeostasis: A Study of Antioxidant Capacity, Oxidative Stress, and the Protective Effects of Emodin

Priyanka Saha

184-200

IL-2/IL-4 stimulation enhances the diagnostic yield of chromosomal abnormalities in Multiple Myeloma.

Sugandhini D

221-198

Insights into Parkinson’s Disease-specific α-Synuclein’s nuclear physiological role

Archanalakshmi Kambaru

387-197

Mutation spectrum of ALMS1 gene in Alstrom syndrome

Soumittra Nagasamy

319-196

Gene expression profile of B-cell subtypes in Granulomatosis with Polyangiitis

Sohini Saha

318-195

Uncovering Novel NOBOX Variants: Genetic basis of Premature Ovarian Insufficiency in three Indian Families.

Anjana Kar

384-193

Effect of Genetic Polymorphisms on treatment outcomes in Lupus Nephritis patients

Azad Jha

250-192

Shared Genetics of Blood Pressure, Smoking and Neurological Disorders in Cross-Ancestry, European and South Asian Populations

Akhilesh Khamkar

245-191

Genetic Counseling and Ethical Considerations in PGT-M for Adult-Onset Hereditary Cancer Syndromes: A Case Report on PALB2 Mutation Prevention

Nupur Mehrotra

275-188

Fusion-Gene Detection Techniques: A Strategic Double-Win Assessment with Open-Source Ph+ ALL and Ph-like ALL RNASeq cohort

Nikha Trivedi

171-187

Prevalence and patterns of chromosomal aneuploidy in a tertiary care center for Neurodevelopmental disorders

Ranjitha M

365-186

Spinocerebellar Ataxia-27B caused by repeat expansion in FGF14 gene in the Indian population

Pannaga Prasad G

379-185

Investigating the link between therapeutic efficacy of lithium and mitochondrial parameters

Manasadeepika .

58-184

Critical Role of Comprehensive Genetic Analysis in Risky Pregnancy: A Case Study

Shweta Jangam

227-183

Theranostic Role of microRNA in Cardiovascular Diseases

Zavia Evangeline Kitherian

361-182

Implications of EXTL2-Driven CSPG Accumulation in CNS for Multiple Sclerosis Progression

Shivani Durai Krishna Kanth

270-181

Reversing Glioblastoma's Epigenetic Defense: The Therapeutic Potential of NPTX2 in Tumor-Neuron Interactions

Krithika Venkatraman

343-179

Bioinformatics Strategies for Decoding the Long-Read Sequencing for Genomic Imprinting Disorders

Venkatesh Rajendran

34-178

Tamoxifen positively regulates the expression of cell adhesion and apoptotic genes in ER/PR-positive Breast Cancer

Ananya Gangaraju

333-177

Contribution of rare sequence variants in cilia and hedgehog pathway genes in Down syndrome associated atrioventricular septal defects

Rashmi Shukla

347-176

Systematic review of transcriptomics studies in bladder cancer reveals the prevalent expression of growth factor receptor genes.

Akshayaa Manikandan

371-174

A rare case report: Idiopathic arterial calcification and hypercholesterolemia in a South Indian young man

Arumugam Suriyam Nagappan

372-172

Comprehensive Assessment of APOL1 Genetic Variants in Chronic Kidney Disease, Focal Segmental Glomerulosclerosis of South India

Preethi Loganathan

230-171

miRNA Cluster Dysregulation in Colorectal Cancer: Mapping Uncharted Paths to Diagnostic Biomarkers

Jayasuriya Munuswamy

374-170

PODOCYTE GENE EXPRESSION PATTERN IN CHILDHOOD NEPHROTIC SYNDROME

C.D.Mohana Priya

359-169

IL-2 Gene Polymorphism: A Key Contributor to Steroid Resistance in Nephrotic Syndrome

Yogalakshmi Venkatachalapathy

363-168

MIRNAS: THE GENE REGULATORS IN PAEDIATRIC NEPHROTIC SYNDROME

Pricilla Charmine

274-167

Variants in SNRPN/SmB cause a variable neurodevelopmental disorder with developmental and behavioral abnormalities in Drosophila melanogaster

Purvi Majethia

247-166

Automated DNA Extraction from Complex Metagenomic Samples Using the MANTA System

Seethal Babu

367-165

Comparative transcriptome of normal and cancer-associated fibroblasts

Apoorva Abikar

289-164

Meta-Analysis of PTH and VDR Gene Associations in Pediatric Nephrotic Syndrome

Janani V

346-163

Survival of the sickest: Gaucher disease as a potential clinical modifier of COVID-19

Prajakta Joshi

362-162

Influence of P2RY12 and CYP2C19 Polymorphisms on Soluble P-Selectin Expression in Coronary Artery Disease Patients Undergoing Clopidogrel monotherapy and Dual- antiplatelet therapy

Bharath Govindaswamy

293-160

THE INFLUENCE OF BGLAP AND SP7 ON BONE MINERALISATION IN PEDIATRIC NEPHROTIC SYNDROME : A SYSTEMATIC REVIEW

Bhuvaneshwari P

291-159

THE ROLES OF SLC34A1 AND AKT1 IN PEDIATRIC NEPHROTIC SYNDROME: A SYSTEMATIC REVIEW

Lakshmi Sai Sindhu Namu

358-158

Molecular genetic analysis of the Anti-Mullerian Hormone (AMH) gene in Polycystic Ovary Syndrome patients from Assam

Adity Paul

360-157

EGFR variant 8 is overexpressed and associated with poor prognosis in oral cancer

Sundaram Reddy Chakkarappan

353-156

A Cost-Effective Digital Microscope Adaptor to Expand Digital Pathology Access in Resource-Limited Settings

Devika Sreevallabhan

180-155

Evaluating the DNA methylation signatures for pharmacoresistance in obsessive-compulsive disorder

Aisha Shaju

208-154

Identifying the Genetic Links Between Dyslipidemia and Myocardial Infarction: Insights into Correlated Genes and MiRNA Networks

Sasitharan Thirumudi

255-153

Parkinson’s disease model system: Development of a PINK1 hiPSC mutant line and standardization of midbrain Dopamine neuron derivation

Surajit Malakar

350-152

FOXP4 related neurodevelopmental disorder with variable expressivity and reduced penetrance

Shrutika Padwal

249-151

Investigating Inherited Deafness in India: Carrier Frequency of GJB2 (Connexin-26) Mutations in Newborns

Ketaki Rajwade

348-150

 HPDB: a comprehensive pigmentation gene database 

 Shwetotpal Mrinal

330-149

Intrinsic apoptotic pathway genes- BCL2, BAX and BAK1 have contrasting association with hormonal receptors ER and PR, and also on HER2 mediated mutation count.

Ananya Kannan

187-148

Evaluating the impact of genetic variants in the binding affinity of muscarinic receptor agonists xanomeline with muscarinic acetylcholine M1 and M4 receptors

Varun Thachan Kundil

315-147

Precise identification of triplet repeat number in Fragile X syndrome by HiFi long-read sequencing

Kritika Ramgopal

317-146

A Scalable Bioinformatics Pipeline Utilizing Long-Range PCR and Oxford Nanopore Sequencing for Efficient Diagnosis of Rare Genetic Diseases

Amit Kumar

276-145

Whole exome sequencing reveals a novel variant in the ATP7A gene for Menkes disease

Charvy Rana

344-144

Streamlining Cancer Detection and Monitoring with Manta’s Automated Extraction Technology

Gayathri Subramanian

334-142

Basal level expression of FDXR, CDKN1A, and DDB2 genes in the blood samples of diabetic, cancer, and healthy participants, and their relevance for triage/biodosimetry

Venkateswarlu Raavi

210-140

Mapping Rare and Uncommon Genetic Variants in Pediatric Disorders of Odisha

Nitish Kumar Mohanta

338-139

Vaginal microbiome with differentially enriched inflammatory pathways are associated with preterm birth in Indian women

Mousumi Sarkar

340-138

Does the type of F8 intron 22 inversion influence FVIII inhibitor development in severe haemophilia A patients?

Karishma Vyas

219-137

Navigating Genetic Risks: The Impact of Carrier Screening on Informed Reproductive Choices in Couples planning for ART Conception

Ishwarya C T

156-136

Is the combination of F8 inversions and TNF-α polymorphism a dangerous synergy for inhibitor development in severe haemophilia A patients??

Sharda Shanbhag

335-132

Distribution of celiac disease associated HLA-DQ haplotypes, risk assessment and tag SNP identification in North Indian population

Priyanka Tiwari

314-131

Pharmaco-epigenomic modulation of miRSNPs and its effect towards Metformin and Myoinositol Drugs in Polycystic Ovary Syndrome

Supraja M Kodanch

234-128

COMMUNICATION GAP IN GENETIC SERVICES

Dr.Rema Devi

157-127

Mission Program on Pediatric Rare Genetic Disorders (PRaGeD)

Neeraja Chilukoti

21-125

The Role of CD36 Polymorphisms and Salivary Factors in Modulating Fat Taste Sensitivity and Obesity Risk

Keerthana Vasanthakumar

324-123

Concomitant telomere attrition is associated with Spinal Muscular Atrophy in highly inbred region of North India

Dil Afroze

320-122

Comparative yield of quantitative fluorescent PCR and low resolution chromosomal microarray in pregnancies with ultrasonographic abnormalities

Mary Purna Chacko

301-121

Targeting Beta-lactamase activity with Oxacyclohexadecan-2-one in Carbapenem-resistant Uropathogenic E. coli: A Molecular simulation approach

Priyanka Balaji

306-119

OBTAINING 3-DIMENSIONAL CULTURES OF MDA-MB-231 (HUMAN BREAST CANCER CELL LINE) – AN APPROACH FOR INDUCING IN VIVO-RELEVANT GENE EXPRESSIONS TOWARDS PERSONALIZED MEDICINE

Farheen Fathima

305-116

Molecular Studies on Consequences of Mutations in ANTXR2 on Subcellular Localization and Protein Aggregation

Gurudatta Bv Baraka

148-115

Characterization of SHQ1 gene variants: Case Studies of Global Developmental Delay and Dystonia in Pediatric Patients

Gowri Rao

290-113

Genetic variability of human SLCO1B1 and statin response: A systematic review and meta-analysis

Atchaya Manoharan

159-112

Effects of ABCB1 and CETP gene polymorphism on the pharmacokinetics of statins: Systematic review and Meta-analysis

Priyanka G

151-111

Frequency of ABCG2 gene polymorphism and its impact on statin treatment response in patients with cardiovascular diseases: A systematic review and Meta-Analysis

Anoushka Rajashekhar

286-110

Meta-Analysis of miRNA Variants Associated with Susceptibility to Autism Spectrum Disorder

Bharathippriyan D

260-108

Phenotyping and genotyping of unclassified heritable thrombocytopenia and platelet function disorders.

Nikesh Kawankar

264-107

Genome wide methylation analysis unravels the genes responsible for postpartum reversal of gestational diabetes mellitus

Sibin M K

277-106

GA4GH: Foundational products for broad and responsible genomic data sharing

Reggan Thomas

213-105

Unveiling The Protein Structural and Dynamical Consequences of Variants of Uncertain Significance in Parkinson's Disease

Anitha S

139-104

Correlation of Chromosomal aberration with Multiorgan dysfunction in Perinatal Asphyxia.

Dr. Manoj A

206-101

Decoding Brain Ageing and its Radiological Genomics Signature: A Patient-individualized therapeutic approach to neurodegenerative disease using anatomically-varying cerebral transcriptomics profile.

Bhaskar Roy

29-100

COMPLEXITY OF A MENDELIAN DISEASE: CAN VARIANTS IN ATP7B AND MODIFIER LOCI REGULATE COGNITIVE DECLINE AND OTHER CLINICAL MANIFESTATIONS IN WILSON DISEASE?

Arpan Saha

186-99

Role of BDNF genetic variants in determining sleep quality in individuals with schizophrenia

Anusree A Kumar .

175-98

Novel biallelic intronic variant, c.172+5G>A in WWOX leads to aberrant splicing

Niha Ashreen

223-97

Novel biallelic variants in AHR causing foveal hypoplasia 3

B N Spoorthi

268-96

Crosstalk between genetics and epigenetics in nonsyndromic hearing loss

Ardra M

162-95

Genetic Markers of Dyslipidemia in Indian Adolescents

Janaki M. Nair

178-94

Rare genetic variants in circadian rhythm and sleep homeostasis genes among attention deficit hyperactivity disorder

Jasmine John

266-93

Sexual antagonism in the multivariate genetic architecture of contemporary humans

Anasuya Chakrabarty

265-92

Tubular cell mitochondria in renal disorder

Dibyajyoti Boruah

181-91

Exploring the Anti-Cancer Potential of Murraya species through Molecular Docking and ADMET Approach Targeting Key Cancer Receptors

Anmol Kaur

198-90

Study of molecular prognostics in Myelodysplastic Syndromes: The Impact of Gene Mutations on Clinical Outcomes

Nehakumari Maurya

257-89

Identification of Molecular Biomarkers for Improved Tumor and Non-Tumor Demarcation in Oral Squamous Cell Carcinoma

Kashish Gupta

177-88

Pulmonary Embolism With Underlying Family History Presenting as Syncope: A Case Report

Amruta Chavhan

199-87

Clinical and Molecular Findings in a Male Child with 47,XX,+i(Y)(p10)/46,XX Mosaicism: Implications for Genetic Counseling and Management

Gopika K N

225-86

Association of genetic variants with Rheumatoid Factor and Anti-CCP in deciphering heterogeneity between Rheumatoid Arthritis Patients

Shreya Johnson

251-85

Clinical implications of CFHR1/CFHR3 partial deletions

Akhauri Yash Sinha

42-84

Systems biology-Driven Hub Gene Analysis with Molecular Docking and ADMET Studies for Natural Compound-Based Therapeutics in Oral Cancer.

Urvi Urvi

229-81

Precision Therapy in Hepatocellular and Pancreatic Cancers: Targeting Oncogenic Drivers and Modulating Immune Responses

Joys Rachel Immanuel

243-80

Temporal gene expression signatures across neurodevelopment: a transdiagnostic analysis of bipolar disorder, schizophrenia, autism, and epilepsy

Kalyani Karunakaran

215-79

Nucleolin Overexpression: A Key Genetic Factor in Tumorigenesis

Janani Balaji

202-78

Comprehensive Assessment of Tyrosine Kinase Domain Mutations and Imatinib Resistance in Chronic Myeloid Leukemia

Somprakash Dhangar

127-77

A Case Study on SCARB1 gene mutation in relation to hypercholesterolemia.

Keerthana B M

238-76

Exploring Ciliary Syndromic Variability through Molecular Clusters Derived from Ayurveda-Informed Phenotypes

Ashish Sharma

109-73

Modelling ALS: Development of an iPSC based platform for disease mechanism studies

Saileyee Roychowdhury

236-72

Genetic Diversity and Heritage Crafting in the Artisan Communities of Thar's Legacy

Rishabh Jain

235-71

PROMOTER AND EXONIC VARIATIONS IN HYPOTHALAMIC-GONADAL AXIS-RELATED GENES AMONG SOUTH INDIAN WOMEN WITH POLYCYSTIC OVARY SYNDROME

Jijo Francis

55-69

To perform in Silico analysis of SNPs of Toll like Receptor 9 (TLR9).

Archit Varshney

232-68

The Antioxidant Paradox in Cancer Therapy: A Double-Edged Sword in Tumor Progression and Treatment Resistance

Tina S Biju

231-67

Genetic association analysis of KISS1 polymorphism (rs5780218) with Polycystic Ovary Syndrome in Northwest Indian population

Anshika Anshika

222-66

To Investigate the association analysis of GnRH I polymorphism (rs6185) with PCOS in the Punjab region.

Mrigakshi Mrigakshi

149-65

Promoter hypermethylation of FHIT and re-expression by 5-aza-2’-deoxycytidine treatment in gastric cancer cell line

Ms. Juhi Singh

212-64

Title: Whole Exome Sequencing Reveals UNC45B As a Novel Candidate Gene Associated With Dilated Cardiomyopathy

Amrita Mukhopadhyay

201-63

miR-34a and miR-221 expression upon in vitro Lithium and valproate exposure to Bipolar Disorder patients-derived LCLs

Akshayaa Ganesh

116-62

Investigating the effects of homozygosity upon the genetic underpinnings of cardiometabolic and cognitive phenotypes

Siddhi Jani

200-61

Unraveling the clinical significance of missense SNPs in PCSK9, LDLRAP1 and LIPA genes in hypercholesterolemia through in silico approach

Vanshikaa K

205-60

Centre-Specific Portrait of Muscular Dystrophies in Gujarat: Insight into Genetic Diagnosis and Management

Gaurang Sindhav

209-59

Investigating the role of microRNAs (miRNAs) during psoriasis pathogenesis

Urbee Banerjee

207-58

Genetic analysis of FABP4 rs8192688 and rs112313579 polymorphisms in Post menopausal Obese Women

Nair Meenakshi

146-57

Computational Strategies in Identifying Therapeutic Targets and Drug Screening for Dystrophinopathies

Pooja Trivedi

203-56

Investigating the contributions of accessible chromatin regions in the epidermal keratinocytes during psoriasis pathogenesis.

Saikat Karuri

191-55

To Study the therapeutic efficacy of Annona muricata (Lakshmanaphala) fruit extract for Oral cancer and identify molecular targets

Rajeswari Narayanappa

54-54

Whole Exome sequencing for assessing the genetic heterogeneity in Aplastic anaemia in eastern region of India

Rojina Yasmin

164-53

CAG repeat instability and region-specific gene expression changes in the SCA12 brain

Shreevidya Parthaje

188-52

Gene Expression Analysis of Pro-inflammatory Cytokine (TNF-α) Gene in Major Depressive Disorder

Yuvapriya K Kalidasan

194-51

IL-18 PROMOTER REGION GENE VARIATIONS (-607 C>A AND -137 G>C) AND GENE EXPRESSION IN PCOS: A STUDY FROM INDIA.

Roger Francis

173-50

MULTI-MODAL ANALYSIS OF BREAST CANCERS USING PAIRED SCRNA-WXS SEQUENCING REVEALS DRIVER MUTATION EFFECTS ON TUMOR MICROENVIRONMENT

Tuneer Mallick

47-49

miR-605 rs2043556 A/G Polymorphism and Breast Cancer Risk in Patients from Punjab: A Case-Control Study

Tanisha Sharma

192-48

“SYNONYMOUS AND NONSYNONYMOUS NOVEL MUTATIONS IN COMT GENE IN SCHIZOPHRENIA PATIENTS: IN CASE-CONTROL IN TUMKUR DISTRICT IN SOUTH KARNATAKA”

Ramesh Babu

84-47

VEGFR2-604T/C Promoter Polymorphism and Breast Cancer Risk in Patients from Punjab

Ranjot Kaur

44-46

Association of miR196a2 rs11614913 Polymorphism with Breast Cancer Risk

Bhargavi Mahajan

152-45

An integrative methylome-transcriptome study reveals PRDM1 coordinates with JUNB to act as an epigenetic regulator in Psoriasis pathogenesis

Soham Saha

174-43

An optimized instrument variable selection approach to improve causality estimation in association studies

Jyoti Sharma

179-42

Genomic Insights and Functional Analysis in Young Familial Myocardial Infarction.

Sayali Shinde

176-41

EGFR variant 8 is overexpressed and associated with poor prognosis in oral cancer

Sundaram Reddy Chakkarappan

168-40

Repurposing the TGF beta inhibitors to rescue the expression of hepcidin to combat iron overload among β- thalassemia patients

Prajwal G

53-39

NLRP3 and AIM2 inflammasome gene expression in response to IFNα in Systemic Lupus Erythematosus (SLE)

Swapnal R. Pawaskar

166-38

ScInfeR: an efficient method for annotating cell types and sub-types in single-cell RNA-seq, ATAC-seq, and spatial omics

Asish Swain

130-37

Unraveling Shared Molecular Mechanisms between Schizophrenia and Type-2 Diabetes Mellitus through Advanced Weighted Gene Co-Expression Network Analysis

Rajveer Singh Shekhawat

161-36

Computational Identification and Characterisation of Novel miRNAs Involved in β-thalassemia

Sumayakausar S Kalaigar Kalaigar

97-35

Elevated ferritin levels suppress has-miR-6743-5p expression and aid in upregulation of hepcidin among Transfusion Dependent β-Thalassemia

Dr. Jyothi M N

153-33

The next era of cytogenetic testing: Harnessing the power of “cell-free mitotic factors” for rapid prophasing of interphase chromatin

Krithika Rajesh

150-32

Maternal NLRP3 Activation and Fetal NKX2-5 Expression in Aborted Fetuses with Suspected Congenital Heart Defects

Dr. Dinesh Roy D

52-31

Standardization of In Vitro Culture, Expansion, and Isolation of Primary Fibroblasts from Human Skin Punch Biopsy to Assess Germline Variants in Myeloid Leukemia

Parampreet Kour

145-30

DNA Methylation analysis of OPRM1, DAT1 and DRD2 genes in drug dependent population of Manipur.

Hemam Raishowriya Devi

142-29

Genetic association of IL1B gene variants with primary glaucoma in a North Indian Punjabi cohort: An original study and meta-analysis

Sanjana Mehrotra

51-28

An analysis of patterns of inheritance in familial primary concomitant strabismus in a homogenous south Asian population

Zia Chaudhuri

123-27

ANALYZING THE ROLE OF SRD5A2 (rs523349) IN POLYCYSTIC OVARY SYNDROME

Mary Martin

140-26

Application of Caffeine Consume in High Concentration can be Harmful or Exaggerated in the Central Nervous System of Human and also used when, as like an Effective Pesticide in Agriculture — Whether A Comparative study using Drosophila melanogaster as a m

Atreyee Majumder

136-25

Human mitochondrial genome analysis using long reads to identify disease causing variants: a systematic evaluation & comparison with short read approach

Jyoti Mridha

110-24

Evaluating the contribution of complex chromosomal rearrangements in pregnancy loss: A critical aspect of reproductive genetics

Vidya Bhairi

118-23

Human mitochondrial genome analysis using long reads to identify disease causing variants: a systematic evaluation & comparison with short read approach

Jyoti Mridha

101-21

Mutations in HYPK cause a novel neurodevelopmental disorder by impairing neuronal proteostasis and autophagy

Smita Saha

125-20

Chromosomal Alterations and Epigenetic Modification of Prader Willi Syndrome patients from Tamil Nadu, India

Padmavathi Vijayakumar

114-19

Effect of Yoga-Primed Serum from Male Infertile Cohort on Cancer Cell Behavior

Anjali Yadav

124-18

Effect of Mindfulness Meditation on IOP, Gene Expression, and Mitochondrial Markers in Primary Open-Angle Glaucoma (POAG).

Manoj Kumar

96-17

Analysis of chromosomal aberrations in the centromeric regions of Alcohol consumers

Prathipa Ramesh

112-16

Understanding the role of genomic variations in women delivering early preterm

Rishika Maji

92-15

Unravelling disease severity in viral infections: The role of CD4+ T cell specific eQTLs in COVID-19

Supratim Ghosh

99-14

Comprehensive Profiling of Neurodegenerative and Inflammatory Biomarkers in Alzheimer’s Disease: Insights for Early Diagnosis and Targeted Therapy

Prabhakar Tiwari

77-13

First Genome-Wide Association Study of Type 2 Diabetes in Population of Jammu and Kashmir

Mansi Rajput

90-12

Expression profile of the SBSPON gene in the Type 2 Diabetes Individuals

Itty Sethi

82-11

An investigation of stress, 5-HTTLPR polymorphism and cytokine in etiopathology of depression: A study among patients in Sikkim, India

Bisu Singh

69-10

AN UPDATE ON THE BRCA1 AND BRCA2 GENE MUTATION SPECTRUM: LARGEST DATASET FROM A SINGLE CENTRE IN INDIA

Pratibha Yadav

27-Jun

Decoding the genetic blueprint of sleep quality and subjective well-being in young adults

Semantee Ray

43-07

Genetic Landscape of Polycystic Ovary Syndrome (PCOS)

Ashutosh Halder

49-09

Genetic Modulation of Airway Remodelling genes and their associated risk towards Chronic Obstructive Pulmonary Disease (COPD) in North Indian Population

Heena Kansal

48-08

Genetic variant rs1527423 T>C in microRNA-25 is associated with an increased risk of Chronic Obstructive Pulmonary Disease (COPD) in the North Indian Population

Anmol Bhatia