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Intraoperative Navigation Is Associated with Reduced Blood Loss During C1–C2 Posterior Cervical Fixation

World neurosurgery, 2017-11, Vol.107, p.574-578

2017

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NMDA receptor-independent control of transcription factors and gene expression

Neuroreport, 2009-10, Vol.20 (16), p.1429-1433

2009

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NMDA receptor-independent control of transcription factors and gene expression

Neuroreport, 2009-10, Vol.20 (16), p.1429-1433

2009

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The effect and evolution of patient selection on outcomes in endoscopic third ventriculostomy for hydrocephalus: A large-scale review of the literature

Journal of the neurological sciences, 2018-02, Vol.385, p.185-191

2018

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Hippocampal gamma‐slow oscillation coupling in macaques during sedation and sleep

Hippocampus, 2017-11, Vol.27 (11), p.1125-1139

2017

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Ultrasonography Detects Ulnar Nerve Dislocation Despite Normal Electrophysiology and Magnetic Resonance Imaging

World neurosurgery, 2017-03, Vol.99, p.809.e1-809.e5

2017

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Improved Postoperative Metrics with Modified Myofascial Closure in Fetal Myelomeningocele Repair

Operative neurosurgery (Hagerstown, Md.), 2020-02, Vol.18 (2), p.158-165

2020

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2023 Update on European Atherosclerosis Society Consensus Statement on Homozygous Familial Hypercholesterolaemia: new treatments and clinical guidance

European heart journal, 2023-07, Vol.44 (25), p.2277-2291

2023

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Not just for programmers: How GitHub can accelerate collaborative and reproducible research in ecology and evolution

Methods in ecology and evolution, 2023-06, Vol.14 (6), p.1364-1380

2023

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ClinGen — The Clinical Genome Resource

The New England journal of medicine, 2015-06, Vol.372 (23), p.2235-2242

2015

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Multimaterial Dual Gradient Three-Dimensional Printing for Osteogenic Differentiation and Spatial Segregation

Tissue engineering. Part A, 2020-03, Vol.26 (5-6), p.239-252

2020

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Perinatal features of the RASopathies: Noonan syndrome, Cardiofaciocutaneous syndrome and Costello syndrome

American journal of medical genetics. Part A, 2014-11, Vol.164A (11), p.2814-2821

2014

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A rare human centenarian variant of SIRT6 enhances genome stability and interaction with Lamin A

The EMBO journal, 2022-11, Vol.41 (21), p.e110393-n/a

2022

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Results from the DC-8 Inlet Characterization Experiment (DICE): Airborne Versus Surface Sampling of Mineral Dust and Sea Salt Aerosols

Aerosol science and technology, 2007-02, Vol.41 (2), p.136-159

2007

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Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1

Human mutation, 2020-01, Vol.41 (1), p.299-315

2020

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KAT6A Syndrome: genotype–phenotype correlation in 76 patients with pathogenic KAT6A variants

Genetics in medicine, 2019-04, Vol.21 (4), p.850-860

2019

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A rare human centenarian variant of SIRT6 enhances genome stability and interaction with Lamin A

The EMBO journal, 2023-02, Vol.42 (3), p.e113326-n/a

2023

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Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay

American journal of medical genetics. Part A, 2012-02, Vol.158A (2), p.391-399

2012

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Correction: KAT6A Syndrome: genotype–phenotype correlation in 76 patients with pathogenic KAT6A variants

Genetics in medicine, 2020-11, Vol.22 (11), p.1920-1920

2020

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KAT6A Syndrome: genotype–phenotype correlation in 76 patientswith pathogenic KAT6A variants

Genetics in medicine, 2019-04, Vol.21 (4), p.850-860

2019

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Implementing stakeholder engagement to explore alternative models of consent: An example from the PREP-IT trials

Contemporary clinical trials communications, 2021-06, Vol.22, p.100787-100787, Article 100787

2021

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Laboratory markers of cardiovascular risk in pediatric SLE: the APPLE baseline cohort

Lupus, 2010-10, Vol.19 (11), p.1315-1325

2010

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Training, competency, and credentialing standards for diagnostic cervicocerebral angiography, carotid stenting, and cerebrovascular intervention: a joint statement from the American Academy of Neurology, the American Association of Neurological Surgeons, the American Society of Interventional and Therapeutic Neuroradiology, the American Society of Neuroradiology, the Congress of Neurological Surgeons, the AANS/CNS Cerebrovascular Section, and the Society of Interventional Radiology

Neurology, 2005-01, Vol.64 (2), p.190-198

2005

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Intraoperative Navigation Is Associated with Reduced Blood Loss During C1–C2 Posterior Cervical Fixation

NMDA receptor-independent control of transcription factors and gene expression

NMDA receptor-independent control of transcription factors and gene expression

The effect and evolution of patient selection on outcomes in endoscopic third ventriculostomy for hydrocephalus: A large-scale review of the literature

Hippocampal gamma‐slow oscillation coupling in macaques during sedation and sleep

Ultrasonography Detects Ulnar Nerve Dislocation Despite Normal Electrophysiology and Magnetic Resonance Imaging

Improved Postoperative Metrics with Modified Myofascial Closure in Fetal Myelomeningocele Repair

2023 Update on European Atherosclerosis Society Consensus Statement on Homozygous Familial Hypercholesterolaemia: new treatments and clinical guidance

Not just for programmers: How GitHub can accelerate collaborative and reproducible research in ecology and evolution

Rationale and design of the familial hypercholesterolemia foundation CAscade SCreening for Awareness and DEtection of Familial Hypercholesterolemia registry

ClinGen — The Clinical Genome Resource

Multimaterial Dual Gradient Three-Dimensional Printing for Osteogenic Differentiation and Spatial Segregation

Perinatal features of the RASopathies: Noonan syndrome, Cardiofaciocutaneous syndrome and Costello syndrome

A rare human centenarian variant of SIRT6 enhances genome stability and interaction with Lamin A

Results from the DC-8 Inlet Characterization Experiment (DICE): Airborne Versus Surface Sampling of Mineral Dust and Sea Salt Aerosols

Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1

KAT6A Syndrome: genotype–phenotype correlation in 76 patients with pathogenic KAT6A variants

A rare human centenarian variant of SIRT6 enhances genome stability and interaction with Lamin A

Erratum To: A rare human centenarian variant of SIRT6 enhances genome stability and interaction with Lamin A

Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay

Correction: KAT6A Syndrome: genotype–phenotype correlation in 76 patients with pathogenic KAT6A variants

KAT6A Syndrome: genotype–phenotype correlation in 76 patientswith pathogenic KAT6A variants

Implementing stakeholder engagement to explore alternative models of consent: An example from the PREP-IT trials

Laboratory markers of cardiovascular risk in pediatric SLE: the APPLE baseline cohort

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