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

27-06

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

34

Molecular Landscaping of Primary & Metastatic Brain Neoplasms

Rakesh Rawal

126

Molecular genetic testing in a cohort of patients with cardiomyopathy

Vandana Kamath

199

Antisense Oligonucleotides Mediated Rescue of ATM Mis-splicing

Akhila Sankar

901

Differential Expression Of miRNA’S In Coronary Artery Disease

Vinodhini Subramanian

907

Genetic and Clinical Correlations in Cardiomyopathy in Dakshina Kannada

Rajasekhar Moka

908

A Novel Frameshift BRCA2 Gene Deleterious Variant in TNBC setting: A possible candidate for Poly (ADP-Ribose) Polymerase Inhibitors

Amit Roy Chowdhury

909

Clinical exome sequencing identifies, two homozygous LOXHD1 variants in two inbred families with pre-lingual hearing loss from South India

Mathuravalli Krishnamoorthy

910

Role of genetic factors in Thrombosis during pregnancy and puerperium

Christhunesa S. Christudass

911

Benign breast disease with association of single Nucleotide Polymorphism of Codon 72

Anjani Jalaj

912

Clinical, genetic and structural delineation of RPL13-related spondyloepimetaphyseal dysplasia suggest extra-ribosomal functions of eL13

Prince Jacob

913

Identification of novel gene variants for Autism Spectral Disorders using Whole Exome Sequencing

Ketan Kumar A

914

Understanding the role of IFN-γ/ IL12 immune-axis in Guillian-Barre Syndrome

N R Soumya

915

Investigating the Efficacy of Medhya rasayana on Alzheimer Disease induced Mouse Model

Swathi Maruthiyodan

916

Identification of novel gene variants for Autism Spectral Disorders using Whole Exome Sequencing.

Ketan Kumar A