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Next-generation visitation models using social media to estimate recreation on public lands

Scientific reports, 2020-09, Vol.10 (1), p.15419-15419, Article 15419

2020

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Disruption of contactin 4 in three subjects with autism spectrum disorder

Journal of medical genetics, 2009-03, Vol.46 (3), p.176-182

2009

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In vitro and in vivo comparison of viral and cellular internal ribosome entry sites for bicistronic vector expression

Gene therapy, 2011-06, Vol.18 (6), p.631-636

2011

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Singleton deletions throughout the genome increase risk of bipolar disorder

Molecular psychiatry, 2009-04, Vol.14 (4), p.376-380

2009

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Adjacency externalities and forest fire prevention

Land Economics, 2009-02, Vol.85 (1), p.162-185

2009

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CD24 as a Potential Therapeutic Target in Patients with B-Cell Leukemia and Lymphoma: Current Insights

OncoTargets and therapy, 2022-11, Vol.15, p.1391-1402

Christian, Sherri L

2022

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Oncogenic Ras expression increases cellular formate production

Amino acids, 2021-10, Vol.53 (10), p.1589-1595

2021

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Oncogenic Ras inhibits IRF1 to promote viral oncolysis

Oncogene, 2015-07, Vol.34 (30), p.3985-3993

2015

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Large Genomic Duplicons Map to Sites of Instability in the Prader-Willi/Angelman Syndrome Chromosome Region (15q11–q13)

Human molecular genetics, 1999-06, Vol.8 (6), p.1025-1037

1999

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Methylation-specific PCR simplifies imprinting analysis

Nature genetics, 1997-05, Vol.16 (1), p.16-17

1997

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Maternal Meiosis I Non-Disjunction of Chromosome 15: Dependence of the Maternal Age Effect on Level of Recombination

Human molecular genetics, 1998-06, Vol.7 (6), p.1011-1019

1998

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Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients

American journal of human genetics, 1995-07, Vol.57 (1), p.40-48

1995

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The spectrum of mutations in UBE3A causing Angelman syndrome

Human molecular genetics, 1999, Vol.8 (1), p.129-135

1999

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Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14

Journal of medical genetics, 2001-01, Vol.38 (1), p.26-34

2001

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Geographic Distance to Extracorporeal Life Support Centers for Pediatric Patients Within the Continental United States

Pediatric critical care medicine, 2021-11, Vol.22 (11), p.e594

2021

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An Evaluation of the Assembly of an Approximately 15-Mb Region on Human Chromosome 13q32–q33 Linked to Bipolar Disorder and Schizophrenia

Genomics (San Diego, Calif.), 2002-05, Vol.79 (5), p.635-658

2002

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Autism as a paradigmatic complex genetic disorder

Annual review of genomics and human genetics, 2004-01, Vol.5 (1), p.379-405

2004

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Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15q

Journal of medical genetics, 2002-03, Vol.39 (3), p.170-177

2002

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The E6-Ap ubiquitin-protein ligase (UBE3A) gene is localized within a narrowed Angelman syndrome critical region

Genome research, 1997-04, Vol.7 (4), p.368

1997

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Polymorphisms at the G72/G30 Gene Locus, on 13q33, Are Associated with Bipolar Disorder in Two Independent Pedigree Series

American journal of human genetics, 2003-05, Vol.72 (5), p.1131-1140

2003

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Mutation screening of two candidate genes from 13q32 in families affected with Bipolar disorder: human peptide transporter (SLC15A1) and human glypican5 (GPC5)

BMC genomics, 2002-10, Vol.3 (1), p.30-30, Article 30

2002

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Two 22q telomere deletions serendipitously detected by FISH

Journal of medical genetics, 1998-11, Vol.35 (11), p.939-942

1998

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Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes

Human genetics, 1997, Vol.99 (1), p.11-17

1997

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Global gene analysis identifying genes commonly regulated by the Ras/Raf/MEK and type I IFN pathways

Genomics data, 2015-06, Vol.4 (C), p.84-87

2015

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Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15

Clinical genetics, 2000-05, Vol.57 (5), p.349-358

2000

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