Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders
Ho, Karen S, Wassman, E Robert, Baxter, Adrianne L, Hensel, Charles H, Martin, Megan M, Prasad, Aparna, Twede, Hope, Vanzo, Rena J, Butler, Merlin G
Published in International journal of molecular sciences (09.12.2016)
Published in International journal of molecular sciences (09.12.2016)
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Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis
Prasad, Aparna, Sdano, Matthew A, Vanzo, Rena J, Mowery-Rushton, Patricia A, Serrano, Moises A, Hensel, Charles H, Wassman, E Robert
Published in BMC medical genetics (20.03.2018)
Published in BMC medical genetics (20.03.2018)
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Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population
Matsunami, Nori, Hadley, Dexter, Hensel, Charles H, Christensen, G Bryce, Kim, Cecilia, Frackelton, Edward, Thomas, Kelly, da Silva, Renata Pellegrino, Stevens, Jeff, Baird, Lisa, Otterud, Brith, Ho, Karen, Varvil, Tena, Leppert, Tami, Lambert, Christophe G, Leppert, Mark, Hakonarson, Hakon
Published in PloS one (14.01.2013)
Published in PloS one (14.01.2013)
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The Temple Grandin Genome: Comprehensive Analysis in a Scientist with High-Functioning Autism
Vanzo, Rena J, Prasad, Aparna, Staunch, Lauren, Hensel, Charles H, Serrano, Moises A, Wassman, E Robert, Kaplun, Alexander, Grandin, Temple, Boles, Richard G
Published in Journal of personalized medicine (29.12.2020)
Published in Journal of personalized medicine (29.12.2020)
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Journal Article
Predisposition Locus for Major Depression at Chromosome 12q22-12q23.2
Abkevich, Victor, Camp, Nicola J., Hensel, Charles H., Neff, Chris D., Russell, Deanna L., Hughes, Dana C., Plenk, Agnes M., Lowry, Michael R., Richards, R. Lynn, Carter, Catherine, Frech, Georges C., Stone, Steven, Rowe, Kerry, Chau, Chi Ai, Cortado, Kathleen, Hunt, Angelene, Luce, Karanina, O’Neil, Gayanne, Poarch, Jeff, Potter, Jennifer, Poulsen, Gregg H., Saxton, Heidi, Bernat-Sestak, Michelle, Thompson, Victor, Gutin, Alexander, Skolnick, Mark H., Shattuck, Donna, Cannon-Albright, Lisa
Published in American journal of human genetics (01.12.2003)
Published in American journal of human genetics (01.12.2003)
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A Major Predisposition Locus for Severe Obesity, at 4p15-p14
Stone, Steven, Abkevich, Victor, Hunt, Steven C., Gutin, Alexander, Russell, Deanna L., Neff, Chris D., Riley, Robyn, Frech, Georges C., Hensel, Charles H., Jammulapati, Srikanth, Potter, Jennifer, Sexton, David, Tran, Thanh, Gibbs, Drew, Iliev, Diana, Gress, Richard, Bloomquist, Brian, Amatruda, John, Peter Rae, M.M., Ted Adams, D., Mark Skolnick, H., Shattuck, Donna
Published in American journal of human genetics (01.06.2002)
Published in American journal of human genetics (01.06.2002)
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Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf–Hirschhorn syndrome
Ho, Karen S, South, Sarah T, Lortz, Amanda, Hensel, Charles H, Sdano, Mallory R, Vanzo, Rena J, Martin, Megan M, Peiffer, Andreas, Lambert, Christophe G, Calhoun, Amy, Carey, John C, Battaglia, Agatino
Published in Journal of medical genetics (01.04.2016)
Published in Journal of medical genetics (01.04.2016)
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Abnormally Methylated FMR1 in Absence of a Detectable Full Mutation in a U.S.A Patient Cohort Referred for Fragile X Testing
Hensel, Charles H, Vanzo, Rena J, Martin, Megan M, Ling, Ling, Aliaga, Solange M, Bui, Minh, Francis, David I, Twede, Hope, Field, Michael H, Morison, Jonathon W, Amor, David J, Godler, David E
Published in Scientific reports (25.10.2019)
Published in Scientific reports (25.10.2019)
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Journal Article
Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders
Serrano, Moises, Wassman, E. Robert, Mowery-Rushton, Patricia, Page, Stephanie, Martin, Megan M., Hensel, Charles H., Harward, Erin, Vanzo, Rena, Twede, Hope, Ho, Karen S., Peiffer, Andreas
Published in BioMed research international (01.01.2016)
Published in BioMed research international (01.01.2016)
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Journal Article
Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders
Wassman, E Robert, Ho, Karen S, Bertrand, Diana, Davis, Kyle W, Martin, Megan M, Page, Stephanie, Peiffer, Andreas, Prasad, Aparna, Serrano, Moises A, Twede, Hope, Vanzo, Rena, Scherer, Stephen W, Uddin, Mohammed, Hensel, Charles H
Published in Neurology. Genetics (01.12.2019)
Published in Neurology. Genetics (01.12.2019)
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Journal Article
Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population
Matsunami, Nori, Hensel, Charles H, Baird, Lisa, Stevens, Jeff, Otterud, Brith, Leppert, Tami, Varvil, Tena, Hadley, Dexter, Glessner, Joseph T, Pellegrino, Renata, Kim, Cecilia, Thomas, Kelly, Wang, Fengxiang, Otieno, Frederick G, Ho, Karen, Christensen, Gerald B, Li, Dongying, Prekeris, Rytis, Lambert, Christophe G, Hakonarson, Hakon, Leppert, Mark F
Published in Molecular autism (27.01.2014)
Published in Molecular autism (27.01.2014)
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Semaphorin 3F gene from human 3p21.3 suppresses tumor formation in nude mice
RUIHUA XIANG, DAVALOS, Albert R, HENSEL, Charles H, ZHOU, Xiao-Jun, TSE, Christin, NAYLOR, Susan L
Published in Cancer research (Chicago, Ill.) (01.05.2002)
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Published in Cancer research (Chicago, Ill.) (01.05.2002)
Journal Article
Genome-wide linkage analyses of extended Utah pedigrees identifies loci that influence recurrent, early-onset major depression and anxiety disorders
Camp, Nicola J., Lowry, Michael R., Richards, R. Lynn, Plenk, Agnes M., Carter, Catherine, Hensel, Charles H., Abkevich, Victor, Skolnick, Mark H., Shattuck, Donna, Rowe, Kerry G., Hughes, Dana C., Cannon-Albright, Lisa A.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.05.2005)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.05.2005)
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Journal Article
Isolation of the Human Semaphorin III/F Gene (SEMA3F) at Chromosome 3p21, a Region Deleted in Lung Cancer
Xiang, Rui-Hua, Hensel, Charles H., Garcia, Dawn K., Carlson, Helene C., Kok, Klaas, Daly, Maria C., Kerbacher, Karen, van den Berg, Anke, Veldhuis, Patrick, Buys, Charles H.C.M., Naylor, Susan L.
Published in Genomics (San Diego, Calif.) (15.02.1996)
Published in Genomics (San Diego, Calif.) (15.02.1996)
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Linkage of body mass index to chromosome 20 in Utah pedigrees
HUNT, Steven C, ABKEVICH, Victor, WEAVER-FELDHAUS, Jane, MACALMA, Tess, RICHARDS, Maria M, GRESS, Richard, FRANCIS, Mike, THOMAS, Alun, FRECH, Georges C, ADAMS, Ted D, SHATTUCK, Donna, STONE, Steven, HENSEL, Charles H, GUTIN, Alexander, NEFF, Chris D, RUSSELL, Deanna L, TRAN, Thanh, XIANKANG HONG, JAMMULAPATI, Srikanth, RILEY, Robyn
Published in Human genetics (01.09.2001)
Published in Human genetics (01.09.2001)
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