Contributing Reviewers in 202

Diao, Fei-Yu

Alpelisib: A Well-Tolerated Treatment Option for Patients with HR-Positive, HER2-Negative, PIK3CA-Mutated Advanced Breast Cancer

Ozturkler, Ziya; Kalkan, Rasime

A New Perspective of COVID-19 Infection: An Epigenetics Point of View

Aykac, Asli; Kalkan, Rasime

Epigenetic Approach to PTSD: In the Aspects of Rat Models

Kanduc, Darja

From Genetics to Epigenetics: Top 4 Aspects for Improved SARS-CoV-2 Vaccine Designs as Paradigmatic Examples

Hegde, Rajat; Hegde, Smita; Kulkarni, Suyamindra S.; Pandurangi, Aditya; Gai, Pramod B.; Das, Kusal K.

Genetic Analysis of Neuroligin 4Y Gene in Autism Population of India

Kalayci Yigin, Aysel; Duz, Mehmet Bugrahan; Seven, Mehmet

Rare Findings in Cleidocranial Dysplasia Caused by RUNX Mutation

Atli, Emine Ikbal; Atli, Engin; Yalcintepe, Sinem; Demir, Selma; Kalkan, Rasime; Akurut, Cisem; Ozen, Yasemin; Gurkan, Hakan

Investigation of Genetic Alterations in Congenital Heart Diseases in Prenatal Period

Ganaraja, Valakunja H.; Polavarapu, Kiran; Bardhan, Mainak; Preethish-Kumar, Veeramani; Leena, Shingavi; Anjanappa, Ram M.; Vengalil, Seena; Nashi, Saraswati; Arunachal, Gautham; Gunasekaran, Swetha; Mohan, Dhaarini; Raju, Sanita; Unnikrishnan, Gopikrishnan; Huddar, Akshata; Ravi-Kiran, Valasani; Thomas, Priya T.; Nalini, Atchayaram

Disease Progression and Mutation Pattern in a Large Cohort of LGMD R1/LGMD 2A Patients from India

Atli, Emine Ikbal; Atli, Engin; Yalcintepe, Sinem; Demir, Selma; Mail, Cisem; Eker, Damla; Ozen, Yasemin; Gurkan, Hakan

Clinical Features of Aberrations Chromosome 22q: A Pilot Study

Pomarino, David; Thren, Johanna Ronja; Thren, Anneke; Rostasy, Kevin; Schoenfeldt, Jan

Toe Walking as the Initial Symptom of a Spinocerebellar Ataxia 13 in a Patient Presenting with a Mutation in the KCNC3 Gene

Poon, Kok-Siong; Tan, Karen Mei-Ling

Variant Curation is Crucial to Claim Digenic Inheritance in Juvenile Open Angle Glaucoma