Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Sujit Maiti
Ontogenetic De Novo Copy Number Variations (CNVs) as a Source of Genetic Individuality: Studies on Two Families With MZD Twins for Schizophrenia
PLoS ONE
Multidisciplinary
Related publications
Copy-Number Variations Observed in a Japanese Population by BAC Array CGH: Summary of Relatively Rare CNVs
Journal of Biomedicine and Biotechnology
Functional and Population Genetic Features of Copy Number Variations in Two Dairy Cattle Populations
BMC Genomics
Biotechnology
Genetics
Assessment of Copy Number Variations in the Brain Genome of Schizophrenia Patients
Molecular Cytogenetics
Biochemistry
Molecular Medicine
Genetics
Molecular Biology
Germline Copy Number Variation Associated With Mendelian Inheritance of CLL in Two Families
Leukemia
Cancer Research
Oncology
Anesthesiology
Pain Medicine
Hematology
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families
American Journal of Human Genetics
Genetics
Genome-Wide Identification of Copy Number Variations Between Two Chicken Lines That Differ in Genetic Resistance to Marek’s Disease
BMC Genomics
Biotechnology
Genetics
The Rate of De Novo CNVs in Healthy Controls
The Contribution of 7q33 Copy Number Variations for Intellectual Disability
Neurogenetics
Molecular Neuroscience
Genetics
Cellular
Increased De Novo Copy Number Variants in the Offspring of Older Males
Translational Psychiatry
Psychiatry
Molecular Neuroscience
Biological Psychiatry
Mental Health
Cellular