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Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays

PLoS genetics, 2008-08, Vol.4 (8), p.e1000167-e1000167

2008

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A Translational Profiling Approach for the Molecular Characterization of CNS Cell Types

Cell, 2008-11, Vol.135 (4), p.738-748

2008

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Alzheimer's disease is associated with reduced expression of energy metabolism genes in posterior cingulate neurons

Proceedings of the National Academy of Sciences - PNAS, 2008-03, Vol.105 (11), p.4441-4446

2008

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Recessive Symptomatic Focal Epilepsy and Mutant Contactin-Associated Protein-like 2

The New England journal of medicine, 2006-03, Vol.354 (13), p.1370-1377

2006

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Whole exome sequencing in females with autism implicates novel and candidate genes

International journal of molecular sciences, 2015-01, Vol.16 (1), p.1312-1335

2015

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Autism and increased paternal age related changes in global levels of gene expression regulation

PloS one, 2011-02, Vol.6 (2), p.e16715-e16715

2011

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Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies

Journal of Neural Transmission, 2008-11, Vol.115 (11), p.1573-1585

2008

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Altered neuronal gene expression in brain regions differentially affected by Alzheimer's disease: a reference data set

Physiological genomics, 2008-04, Vol.33 (2), p.240-256

2008

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Gene expression profiles in anatomically and functionally distinct regions of the normal aged human brain

Physiological genomics, 2007-02, Vol.28 (3), p.311-322

2007

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Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia

Circulation (New York, N.Y.), 2001-01, Vol.103 (4), p.485-490

2001

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Expression profiling of medulloblastoma: PDGFRA and the RAS/MAPK pathway as therapeutic targets for metastatic disease

Nature genetics, 2001-10, Vol.29 (2), p.143-152

2001

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A genome-wide association study for age-related hearing impairment in the Saami

European journal of human genetics : EJHG, 2010-06, Vol.18 (6), p.685-693

2010

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Microarray Analysis of Changes in mRNA Levels in the Rat Retina after Experimental Elevation of Intraocular Pressure

Investigative ophthalmology & visual science, 2004-04, Vol.45 (4), p.1247-1258

2004

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FUS mutations in sporadic amyotrophic lateral sclerosis

Neurobiology of aging, 2011-03, Vol.32 (3), p.550.e1-550.e4

2011

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Scavenger Chemokine (CXC Motif) Receptor 7 (CXCR7) Is a Direct Target Gene of HIC1 (Hypermethylated in Cancer 1)

The Journal of biological chemistry, 2009-07, Vol.284 (31), p.20927-20935

2009

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An expression signature classifies chemotherapy-resistant pediatric osteosarcoma

Cancer research (Chicago, Ill.), 2005-03, Vol.65 (5), p.1748-1754

2005

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Peripheral Delivery of a ROCK Inhibitor Improves Learning and Working Memory

Behavioral neuroscience, 2009-02, Vol.123 (1), p.218-223

2009

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High-content siRNA screening of the kinome identifies kinases involved in Alzheimer's disease-related tau hyperphosphorylation

BMC genomics, 2010-01, Vol.11 (1), p.25-25, Article 25

2010

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A Case Study - NeuBase Therapeutics, Inc

Journal of commercial biotechnology, 2021-04, Vol.26 (2), p.67

Stephan, Dietrich A

2021

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Variation in the large-scale organization of gene expression levels in the hippocampus relates to stable epigenetic variability in behavior

PloS one, 2008-10, Vol.3 (10), p.e3344-e3344

2008

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Mapping of Sudden Infant Death with Dysgenesis of the Testes Syndrome (SIDDT) by a SNP Genome Scan and Identification of TSPYL Loss of Function

Proceedings of the National Academy of Sciences - PNAS, 2004-08, Vol.101 (32), p.11689-11694

2004

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Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance

Human molecular genetics, 2007-06, Vol.16 (12), p.1469-1477

2007

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Presymptomatic risk assessment for chronic non-communicable diseases

PloS one, 2010-12, Vol.5 (12), p.e14338-e14338

2010

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Identification of Somatic Chromosomal Abnormalities in Hypothalamic Hamartoma Tissue at the GLI3 Locus

American journal of human genetics, 2008-02, Vol.82 (2), p.366-374

2008

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An APOE-independent cis-eSNP on chromosome 19q13.32 influences tau levels and late-onset Alzheimer's disease risk

Neurobiology of aging, 2018-06, Vol.66, p.178.e1-178.e8

2018

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Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays

A Translational Profiling Approach for the Molecular Characterization of CNS Cell Types

Alzheimer's disease is associated with reduced expression of energy metabolism genes in posterior cingulate neurons

Recessive Symptomatic Focal Epilepsy and Mutant Contactin-Associated Protein-like 2

Whole exome sequencing in females with autism implicates novel and candidate genes

Autism and increased paternal age related changes in global levels of gene expression regulation

Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies

Altered neuronal gene expression in brain regions differentially affected by Alzheimer's disease: a reference data set

Gene expression profiles in anatomically and functionally distinct regions of the normal aged human brain

Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia

Expression profiling of medulloblastoma: PDGFRA and the RAS/MAPK pathway as therapeutic targets for metastatic disease

A genome-wide association study for age-related hearing impairment in the Saami

Microarray Analysis of Changes in mRNA Levels in the Rat Retina after Experimental Elevation of Intraocular Pressure

FUS mutations in sporadic amyotrophic lateral sclerosis

Scavenger Chemokine (CXC Motif) Receptor 7 (CXCR7) Is a Direct Target Gene of HIC1 (Hypermethylated in Cancer 1)

An expression signature classifies chemotherapy-resistant pediatric osteosarcoma

Peripheral Delivery of a ROCK Inhibitor Improves Learning and Working Memory

High-content siRNA screening of the kinome identifies kinases involved in Alzheimer's disease-related tau hyperphosphorylation

A Case Study - NeuBase Therapeutics, Inc

Variation in the large-scale organization of gene expression levels in the hippocampus relates to stable epigenetic variability in behavior

Mapping of Sudden Infant Death with Dysgenesis of the Testes Syndrome (SIDDT) by a SNP Genome Scan and Identification of TSPYL Loss of Function

Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance

Presymptomatic risk assessment for chronic non-communicable diseases

Identification of Somatic Chromosomal Abnormalities in Hypothalamic Hamartoma Tissue at the GLI3 Locus

An APOE-independent cis-eSNP on chromosome 19q13.32 influences tau levels and late-onset Alzheimer's disease risk

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