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Author Details
Full Name
Manuel L Gonzalez-Garay
Affiliation
College of Medicine, University of Arizona
ORCID
Career Start Year
1992
Papers
44
H Index
22
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36385154
Genome-wide association study of a lipedema phenotype among women in the UK Biobank identifies multiple genetic risk factors.
Eur J Hum Genet
2023
32711186
MicroRNA and protein-coding gene expression analysis in idiopathic pulmonary fibrosis yields novel biomarker signatures associated to survival.
Transl Res
2021
34557198
Whole-Blood Mitochondrial DNA Copies Are Associated With the Prognosis of Acute Respiratory Distress Syndrome After Sepsis.
Front Immunol
2021
33276795
Differential transcriptomics in sarcoidosis lung and lymph node granulomas with comparisons to pathogen-specific granulomas.
Respir Res
2020
33343881
Transcriptomic profiles in pulmonary arterial hypertension associate with disease severity and identify novel candidate genes.
Pulm Circ
2020
31615996
Low Dose Carbon Monoxide Exposure in Idiopathic Pulmonary Fibrosis Produces a CO Signature Comprised of Oxidative Phosphorylation Genes.
Sci Rep
2019
29115856
LPS-induced Acute Lung Injury Involves NF-κB-mediated Downregulation of SOX18.
Am J Respir Cell Mol Biol
2018
30161219
New cases of Glucose-6-Phosphate Dehydrogenase deficiency in Pulmonary Arterial Hypertension.
PLoS One
2018
30161129
Single nucleotide polymorphisms in the MYLKP1 pseudogene are associated with increased colon cancer risk in African Americans.
PLoS One
2018
30462678
Fecal virome composition of migratory wild duck species.
PLoS One
2018
29425463
Genome-Wide Association Study in African Americans with Acute Respiratory Distress Syndrome Identifies the Selectin P Ligand Gene as a Risk Factor.
Am J Respir Crit Care Med
2018
26908612
The effect of non-coding DNA variations on P53 and cMYC competitive inhibition at cis-overlapping motifs.
Hum Mol Genet
2016
26574044
Defective Store-Operated Calcium Entry Causes Partial Nephrogenic Diabetes Insipidus.
J Am Soc Nephrol
2016
27935835
Robust Extracellular pH Modulation by Candida albicans during Growth in Carboxylic Acids.
mBio
2016
27830251
Biomechanisms of Comorbidity: Reviewing Integrative Analyses of Multi-omics Datasets and Electronic Health Records.
Yearb Med Inform
2016
27396937
Gene Correction of iPSCs from a Wiskott-Aldrich Syndrome Patient Normalizes the Lymphoid Developmental and Functional Defects.
Stem Cell Reports
2016
27385965
Whole Exome Sequencing Reveals a Mutation in CRYBB2 in a Large Mexican Family with Autosomal Dominant Pulverulent Cataract.
Mol Syndromol
2016
26855770
A novel mutation in CELSR1 is associated with hereditary lymphedema.
Vasc Cell
2016
25772471
Targeted correction and restored function of the CFTR gene in cystic fibrosis induced pluripotent stem cells.
Stem Cell Reports
2015
26283345
Plasma metabolomic profiles enhance precision medicine for volunteers of normal health.
Proc Natl Acad Sci U S A
2015
24188662
Adult genetic risk screening.
Annu Rev Med
2014
26000024
The road from next-generation sequencing to personalized medicine.
Per Med
2014
25366137
Hypertensive renal injury is associated with gene variation affecting immune signaling.
Circ Cardiovasc Genet
2014
25383712
Evidence for SH2 domain-containing 5'-inositol phosphatase-2 (SHIP2) contributing to a lymphatic dysfunction.
PLoS One
2014
25056448
Diversity in the preimmune immunoglobulin repertoire of SHR lines susceptible and resistant to end-organ injury.
Genes Immun
2014
24667040
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.
Genome Biol
2014
23650393
Lymphatic abnormalities are associated with RASA1 gene mutations in mouse and man.
Proc Natl Acad Sci U S A
2013
24076603
Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism.
Nat Genet
2013
24082139
Personalized genomic disease risk of volunteers.
Proc Natl Acad Sci U S A
2013
18948947
Somatic mutations affect key pathways in lung adenocarcinoma.
Nature
2008
16641997
The DNA sequence, annotation and analysis of human chromosome 3.
Nature
2006
17095691
The genome of the sea urchin Strongylocentrotus purpuratus.
Science
2006
16541075
The finished DNA sequence of human chromosome 12.
Nature
2006
15057822
Genome sequence of the Brown Norway rat yields insights into mammalian evolution.
Nature
2004
12154077
Paclitaxel-dependent mutants have severely reduced microtubule assembly and reduced tubulin synthesis.
J Cell Sci
2002
10381386
Vinblastine induces an interaction between FtsZ and tubulin in mammalian cells.
J Cell Sci
1999
10446152
A beta-tubulin leucine cluster involved in microtubule assembly and paclitaxel resistance.
J Biol Chem
1999
8722572
Significant divergence in nucleotide sequences for beta-tubulin from different laboratory strains of Chinese hamster ovary cells.
DNA Seq
1996
8978820
alpha-Tubulin limits its own synthesis: evidence for a mechanism involving translational repression.
J Cell Biol
1996
7553913
Overexpression of an epitope-tagged beta-tubulin in Chinese hamster ovary cells causes an increase in endogenous alpha-tubulin synthesis.
Cell Motil Cytoskeleton
1995
7519616
Stable expression of heterologous microtubule-associated proteins (MAPs) in Chinese hamster ovary cells: evidence for differing roles of MAPs in microtubule organization.
J Cell Biol
1994
8033994
The presence but not the sequence of the N-terminal peptide in cardiac TnC is important for function.
FEBS Lett
1994
1336617
Prevalence in two mexican cities of human papillomavirus DNA sequences in cervical cancer.
Rev Invest Clin
1992
1344797
[The molecular diagnosis of hereditary diseases. In memoriam Dr. Eduardo Aguirre Pequeño].
Gac Med Mex
1992
1 - 44 of 44
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