Scherer, Stephen W.

Evaluating genetic counseling for individuals with schizophrenia in the molecular age

Costain, G., Esplen, M. J., Toner, B., Scherer, S. W., Meschino, W. S., Hodgkinson, K. A., & Bassett, A. S. (2014) · Schizophrenia Bulletin

Schizophrenia research and treatmentCounseling, Therapy, and Family Dynamics

Cited by 54

Genome-wide association analysis of copy number variation in recurrent depressive disorder

Rucker, J. J. H., Breen, G., Pinto, D., Pedroso, I., Lewis, C. M., Cohen-Woods, S., Uher, R., Schosser, A., Rivera, M., Aitchison, K. J., et al. (2013) · Molecular Psychiatry

Genomic variations and chromosomal abnormalitiesGenetic Associations and Epidemiology

Cited by 51

Genes and pathways implicated in tetralogy of Fallot revealed by ultra-rare variant burden analysis in 231 genome sequences

Manshaei, R., Merico, D., Reuter, M. S., Engchuan, W., Mojarad, B. A., Chaturvedi, R., Heung, T., Pellecchia, G., Zarrei, M., Nalpathamkalam, T., et al. (2020) · Frontiers in Genetics

Genomics and Rare DiseasesCongenital heart defects research

Cited by 36

Heterogeneity in clinical sequencing tests marketed for autism spectrum disorders

Hoang, N., Buchanan, J. A., & Scherer, S. W. (2018) · npj Genomic Medicine

Autism Spectrum Disorder ResearchGenomics and Rare Diseases

Cited by 26

CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology

Oppermann, H., Marcos-Grañeda, E., Weiss, L. A., Gurnett, C. A., Jelsig, A. M., Vineke, S. H., Isidor, B., Mercier, S., Magnussen, K., Zacher, P., et al. (2023) · European Journal of Human Genetics

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 18

Rare copy number variation in extremely impulsively violent males

Vevera, J., Zarrei, M., Hartmannová, H., Jedličková, I., Mušálková, D., Přistoupilová, A., Oliveriusová, P., Trešlová, H., Nosková, L., Hodaňová, K., et al. (2019) · Genes, Brain and Behavior

Psychopathy, Forensic Psychiatry, Sexual OffendingGenomic variations and chromosomal abnormalities

Cited by 15

Variability of Creatine Metabolism Genes in Children with Autism Spectrum Disorder

Cameron, J. M., Levandovskiy, V., Roberts, W., Anagnostou, E., Scherer, S., Loh, A., & Schulze, A. (2017) · International Journal of Molecular Sciences

Autism Spectrum Disorder ResearchMetabolism and Genetic Disorders

Cited by 15

A distributed whole genome sequencing benchmark study

Corbett, R. D., Eveleigh, R., Whitney, J., Barai, N., Bourgey, M., Chuah, E., Johnson, J., Moore, R. A., Moradin, N., Mungall, K. L., et al. (2020) · Frontiers in Genetics

Genomics and Phylogenetic StudiesGenomics and Rare Diseases

Cited by 10

Chromosomal-level reference genome assembly of the North American wolverine (Gulo gulo luscus): a resource for conservation genomics

Lok, S., Lau, T. N. H., Trost, B., Tong, A. H. Y., Wintle, R. F., Engstrom, M. D., Stacy, E., Waits, L. P., Scrafford, M., & Scherer, S. W. (2022) · G3 Genes|Genomes|Genetics

Genomics and Phylogenetic StudiesGenetic diversity and population structure

Cited by 6

Chromosomal-level reference genome assembly of muskox (Ovibos moschatus) from Banks Island in the Canadian Arctic, a resource for conservation genomics

Lok, S., Lau, T. N. H., Trost, B., Tong, A. H. Y., Paton, T., Wintle, R. F., Engstrom, M. D., Gunn, A., & Scherer, S. W. (2024) · Scientific Reports

Genomics and Phylogenetic StudiesGenetic diversity and population structure

Cited by 4