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Neuropathological findings in COVID-19: an autopsy cohort

Journal of neuropathology and experimental neurology, 2023-01, Vol.82 (1), p.21-28

2023

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Novel NOTCH1 mutations in patients with bicuspid aortic valve disease and thoracic aortic aneurysms

The Journal of thoracic and cardiovascular surgery, 2007-08, Vol.134 (2), p.290-296

2007

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From pandemic to endemic: Divergence of COVID-19 positive-tests and hospitalization numbers from SARS-CoV-2 RNA levels in wastewater of Rochester, Minnesota

Heliyon, 2024-03, Vol.10 (6), p.e27974-e27974, Article e27974

2024

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A Comparative Effectiveness Study of Newborn Screening Methods for Four Lysosomal Storage Disorders

International journal of neonatal screening, 2020-06, Vol.6 (2), p.44

2020

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COVID-19-Associated Nonocclusive Fibrin Microthrombi in the Heart

Circulation (New York, N.Y.), 2021-01, Vol.143 (3), p.230-243

2021

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A reverse-transcription droplet digital PCR assay to detect and quantify SARS-CoV-2 RNA in upper respiratory tract specimens

Journal of clinical virology, 2022-08, Vol.153, p.105216-105216, Article 105216

2022

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Evidence of Genetic Locus Heterogeneity for Familial Bicuspid Aortic Valve

The Journal of surgical research, 2007-09, Vol.142 (1), p.28-31

2007

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SARS-CoV-2 RNA detection in Formalin-Fixed Paraffin-Embedded (FFPE) tissue by droplet digital PCR (ddPCR)

Clinica chimica acta, 2022-07, Vol.532, p.181-187

2022

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Comparison of In Situ Hybridization, Immunohistochemistry and Reverse Transcription-Droplet Digital Polymerase Chain Reaction for Severe Acute Respiratory Syndrome Coronavirus 2 (SARSCoV-2)-Testing in Tissue

Archives of pathology & laboratory medicine (1976), 2021-07, Vol.145 (7), p.785-796

2021

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Evaluation of the analytical sensitivity of ACON and LumiraDx SARS-CoV-2 rapid antigen tests using samples with presumed Omicron variant

Diagnostic microbiology and infectious disease, 2023-09, Vol.107 (1), p.115977-115977, Article 115977

2023

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A Droplet Digital PCR Method for Severe Combined Immunodeficiency Newborn Screening

The Journal of molecular diagnostics : JMD, 2017-09, Vol.19 (5), p.755-765

2017

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Comparison of In Situ Hybridization, Immunohistochemistry, and Reverse Transcription-Droplet Digital Polymerase Chain Reaction for Severe Acute Respiratory Syndrome Coronavirus 2

Archives of pathology & laboratory medicine (1976), 2021-07, Vol.145 (7), p.785

2021

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Allelic spectrum of formiminotransferase‐cyclodeaminase gene variants in individuals with formiminoglutamic aciduria

Molecular genetics & genomic medicine, 2017-11, Vol.5 (6), p.795-799

2017

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Myosin light chain phosphatase and kinase abnormalities in fetal sheep pulmonary hypertension

Pediatric research, 1998, Vol.43 (1), p.57-61

1998

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Bicuspid aortic valve and ascending aortic aneurysm are not associated with germline or somatic homeobox NKX2-5 gene polymorphism in 19 patients

The Journal of thoracic and cardiovascular surgery, 2006-06, Vol.131 (6), p.1301-1305

2006

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Effects of calcium channel antagonists on the release of prostaglandin E2 from metabolically stressed muscle

Biochemical pharmacology, 1994-07, Vol.48 (2), p.371-374

1994

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Altered Pattern of Gene Expression in Thoracic Aortic Aneurysms in Patients with Trileaflet and Bileaflet Aortic Valve: A Pilot Study Using Affymetrix Gene Chips

The FASEB journal, 2006-03, Vol.20 (5), p.A1074-A1074

2006

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Abstract 1743: Identification of a Novel Susceptibility Locus at 9q21 for Familial Bicuspid Aortic Valve Disease

Circulation (New York, N.Y.), 2007-10, Vol.116 (suppl_16)

2007

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Elevated expressions of osteopontin and tenascin C in ascending aortic aneurysms are associated with trileaflet aortic valves as compared with bicuspid aortic valves

Cardiovascular pathology, 2007-05, Vol.16 (3), p.144-150

2007

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QS234. TGFBR2 Mutation in Non-Syndromal Thoracic Aortic Aneurysms

The Journal of surgical research, 2008, Vol.144 (2), p.360-360

2008

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Molecular changes occurring with aneurysm formation: Possible impact of sampling error

The Journal of thoracic and cardiovascular surgery, 2006, Vol.131 (1), p.254-255

2006

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A pilot study of spinal muscular atrophy carrier screening in Saudi Arabia

Journal of pediatric neurology, 2007-09, Vol.5 (3), p.221-224

2007

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A Rare Homozygous Missense Mutation in ATP7B Exon 19 in a Case of Wilson Disease

European neurology, 2004-01, Vol.51 (1), p.52-54

2004

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Molecular analysis of the spinal muscular atrophy and neuronal apoptosis inhibitory protein genes in Saudi patients with spinal muscular atrophy

Saudi medical journal, 2003-10, Vol.24 (10), p.1052

2003

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A novel deletion mutation within the carboxyl terminus of the copper-transporting ATPase gene causes Wilson disease

Journal of the neurological sciences, 2000-10, Vol.179 (1), p.140-143

2000

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Neuropathological findings in COVID-19: an autopsy cohort

Novel NOTCH1 mutations in patients with bicuspid aortic valve disease and thoracic aortic aneurysms

From pandemic to endemic: Divergence of COVID-19 positive-tests and hospitalization numbers from SARS-CoV-2 RNA levels in wastewater of Rochester, Minnesota

A Comparative Effectiveness Study of Newborn Screening Methods for Four Lysosomal Storage Disorders

COVID-19-Associated Nonocclusive Fibrin Microthrombi in the Heart

A reverse-transcription droplet digital PCR assay to detect and quantify SARS-CoV-2 RNA in upper respiratory tract specimens

Evidence of Genetic Locus Heterogeneity for Familial Bicuspid Aortic Valve

SARS-CoV-2 RNA detection in Formalin-Fixed Paraffin-Embedded (FFPE) tissue by droplet digital PCR (ddPCR)

Comparison of In Situ Hybridization, Immunohistochemistry and Reverse Transcription-Droplet Digital Polymerase Chain Reaction for Severe Acute Respiratory Syndrome Coronavirus 2 (SARSCoV-2)-Testing in Tissue

Evaluation of the analytical sensitivity of ACON and LumiraDx SARS-CoV-2 rapid antigen tests using samples with presumed Omicron variant

A Droplet Digital PCR Method for Severe Combined Immunodeficiency Newborn Screening

Comparison of In Situ Hybridization, Immunohistochemistry, and Reverse Transcription-Droplet Digital Polymerase Chain Reaction for Severe Acute Respiratory Syndrome Coronavirus 2

Allelic spectrum of formiminotransferase‐cyclodeaminase gene variants in individuals with formiminoglutamic aciduria

Myosin light chain phosphatase and kinase abnormalities in fetal sheep pulmonary hypertension

Bicuspid aortic valve and ascending aortic aneurysm are not associated with germline or somatic homeobox NKX2-5 gene polymorphism in 19 patients

Effects of calcium channel antagonists on the release of prostaglandin E2 from metabolically stressed muscle

Altered Pattern of Gene Expression in Thoracic Aortic Aneurysms in Patients with Trileaflet and Bileaflet Aortic Valve: A Pilot Study Using Affymetrix Gene Chips

Abstract 1743: Identification of a Novel Susceptibility Locus at 9q21 for Familial Bicuspid Aortic Valve Disease

Elevated expressions of osteopontin and tenascin C in ascending aortic aneurysms are associated with trileaflet aortic valves as compared with bicuspid aortic valves

QS234. TGFBR2 Mutation in Non-Syndromal Thoracic Aortic Aneurysms

Molecular changes occurring with aneurysm formation: Possible impact of sampling error

A pilot study of spinal muscular atrophy carrier screening in Saudi Arabia

A Rare Homozygous Missense Mutation in ATP7B Exon 19 in a Case of Wilson Disease

Molecular analysis of the spinal muscular atrophy and neuronal apoptosis inhibitory protein genes in Saudi patients with spinal muscular atrophy

A novel deletion mutation within the carboxyl terminus of the copper-transporting ATPase gene causes Wilson disease

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