Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Britt Johnson
Possible Precision Medicine Implications From Genetic Testing Using Combined Detection of Sequence and Intragenic Copy Number Variants in a Large Cohort With Childhood Epilepsy
Epilepsia Open
Neurology
Related publications
Copy Number Variants Are Frequent in Genetic Generalized Epilepsy With Intellectual Disability
Neurology
Neurology
Detection of Copy Number Variations in Epilepsy Using Exome Data
Clinical Genetics
Genetics
Population Analysis of Large Copy Number Variants and Hotspots of Human Genetic Disease
American Journal of Human Genetics
Genetics
Genetic Copy Number Variants in Myocardial Infarction Patients With Hyperlipidemia
BMC Genomics
Biotechnology
Genetics
Detecting Large Copy Number Variants Using Exome Genotyping Arrays in a Large Swedish Schizophrenia Sample
Molecular Psychiatry
Psychiatry
Molecular Neuroscience
Mental Health
Molecular Biology
Cellular
GSTM1 Copy Number Is Not Associated With Risk of Kidney Failure in a Large Cohort
Frontiers in Genetics
Genetics
Molecular Medicine
A Genome-Wide Study Reveals Copy Number Variants Exclusive to Childhood Obesity Cases
American Journal of Human Genetics
Genetics
High Frequency of Known Copy Number Abnormalities and Maternal Duplication 15q11-Q13 in Patients With Combined Schizophrenia and Epilepsy
BMC Medical Genetics
Genetics
Using ERDS to Infer Copy-Number Variants in High-Coverage Genomes
American Journal of Human Genetics
Genetics
