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Cell-type-specific expression quantitative trait loci associated with Alzheimer disease in blood and brain tissue

Translational psychiatry, 2021-04, Vol.11 (1), p.250-250, Article 250

2021

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A phased SNP-based classification of sickle cell anemia HBB haplotypes

BMC genomics, 2017-08, Vol.18 (1), p.608-608, Article 608

2017

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Set-Based Rare Variant Expression Quantitative Trait Loci in Blood and Brain from Alzheimer Disease Study Participants

Genes, 2021-03, Vol.12 (3), p.419

2021

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Ocular syphilis in an immunocompetent host

IDCases, 2020-01, Vol.19, p.e00684, Article e00684

2020

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Enterovirus D68-associated acute respiratory distress syndrome in adult, United States, 2014

Emerging infectious diseases, 2015-05, Vol.21 (5), p.914-916

2015

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Homozygosity for a haplotype in the HBG2‐OR51B4 region is exclusive to Arab‐Indian haplotype sickle cell anemia

American journal of hematology, 2016-06, Vol.91 (6), p.E308-E311

2016

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Identification of Streptococcus intermedius Central Nervous System Infection by Use of PCR and Electrospray Ionization Mass Spectrometry

Journal of Clinical Microbiology, 2012-12, Vol.50 (12), p.4160-4162

2012

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“Cat got your lung?”: Case of a trapped lung following cat bite

IDCases, 2019-01, Vol.15, p.e00482-e00482, Article e00482

2019

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PCR and Electrospray Ionization Mass Spectrometry for Detection of Persistent Enterococcus faecalis in Cerebrospinal Fluid following Treatment of Postoperative Ventriculitis

Journal of Clinical Microbiology, 2013-10, Vol.51 (10), p.3464-3466

2013

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BCL2L1 is associated with γ-globin gene expression

Blood advances, 2019-10, Vol.3 (20), p.2995-3001

2019

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Transmission of Carbapenem-Resistant Klebsiella pneumoniae in US Hospitals

Clinical infectious diseases, 2023-01, Vol.76 (2), p.229-237

2023

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Association of mitochondrial variants and haplogroups identified by whole exome sequencing with Alzheimer's disease

Alzheimer's & dementia, 2022-02, Vol.18 (2), p.294-306

2022

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PopCluster: an algorithm to identify genetic variants with ethnicity-dependent effects

Bioinformatics (Oxford, England), 2019-09, Vol.35 (17), p.3046-3054

2019

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An association test of the spatial distribution of rare missense variants within protein structures identifies Alzheimer's disease-related patterns

Genome research, 2022-04, Vol.32 (4), p.778-790

2022

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A long noncoding RNA from the HBS1L-MYB intergenic region on chr6q23 regulates human fetal hemoglobin expression

Blood cells, molecules, & diseases, 2018-03, Vol.69, p.1-9

2018

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Novel loci for Alzheimer's disease identified by a genome‐wide association study in Ashkenazi Jews

Alzheimer's & dementia, 2023-12, Vol.19 (12), p.5550-5562

2023

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Corrigendum: An association test of the spatial distribution of rare missense variants within protein structures identifies Alzheimer's disease–related patterns

Genome research, 2022-06, Vol.32 (6), p.1228-1228_1

2022

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Microscopic Review of Nasopharyngeal Swabs as a Means of Benchside Quality Assurance

Annals of clinical and laboratory science, 2020-09, Vol.50 (5), p.665-669

2020

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Genetic determinants of HbF in Saudi Arabian and African Benin haplotype sickle cell anemia

American journal of hematology, 2017-09, Vol.92 (9), p.E555-E557

2017

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Acute respiratory distress caused by Neosartorya udagawae

Medical mycology case reports, 2014-10, Vol.6 (C), p.1-5

2014

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Ureaplasma parvum prosthetic joint infection detected by PCR

Journal of clinical microbiology, 2014-06, Vol.52 (6), p.2248-2250

2014

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Salvage microbiology: opportunities and challenges in the detection of bacterial pathogens following initiation of antimicrobial treatment

Expert review of molecular diagnostics, 2015-03, Vol.15 (3), p.349-360

2015

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The association of HBG2, BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease

International journal of laboratory hematology, 2019-02, Vol.41 (1), p.87-93

2019

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A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression

Blood, 2011-05, Vol.117 (18), p.4935-4945

2011

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Sickle cell leg ulcers: associations with haemolysis and SNPs in Klotho, TEK and genes of the TGF‐β/BMP pathway

British journal of haematology, 2006-06, Vol.133 (5), p.570-578

2006

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Cell-type-specific expression quantitative trait loci associated with Alzheimer disease in blood and brain tissue

A phased SNP-based classification of sickle cell anemia HBB haplotypes

Set-Based Rare Variant Expression Quantitative Trait Loci in Blood and Brain from Alzheimer Disease Study Participants

Ocular syphilis in an immunocompetent host

Enterovirus D68-associated acute respiratory distress syndrome in adult, United States, 2014

Homozygosity for a haplotype in the HBG2‐OR51B4 region is exclusive to Arab‐Indian haplotype sickle cell anemia

Identification of Streptococcus intermedius Central Nervous System Infection by Use of PCR and Electrospray Ionization Mass Spectrometry

“Cat got your lung?”: Case of a trapped lung following cat bite

PCR and Electrospray Ionization Mass Spectrometry for Detection of Persistent Enterococcus faecalis in Cerebrospinal Fluid following Treatment of Postoperative Ventriculitis

BCL2L1 is associated with γ-globin gene expression

Transmission of Carbapenem-Resistant Klebsiella pneumoniae in US Hospitals

Association of mitochondrial variants and haplogroups identified by whole exome sequencing with Alzheimer's disease

PopCluster: an algorithm to identify genetic variants with ethnicity-dependent effects

An association test of the spatial distribution of rare missense variants within protein structures identifies Alzheimer's disease-related patterns

A long noncoding RNA from the HBS1L-MYB intergenic region on chr6q23 regulates human fetal hemoglobin expression

Novel loci for Alzheimer's disease identified by a genome‐wide association study in Ashkenazi Jews

Corrigendum: An association test of the spatial distribution of rare missense variants within protein structures identifies Alzheimer's disease–related patterns

Microscopic Review of Nasopharyngeal Swabs as a Means of Benchside Quality Assurance

Genetic determinants of HbF in Saudi Arabian and African Benin haplotype sickle cell anemia

Acute respiratory distress caused by Neosartorya udagawae

Ureaplasma parvum prosthetic joint infection detected by PCR

Salvage microbiology: opportunities and challenges in the detection of bacterial pathogens following initiation of antimicrobial treatment

The association of HBG2, BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease

A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression

Sickle cell leg ulcers: associations with haemolysis and SNPs in Klotho, TEK and genes of the TGF‐β/BMP pathway

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