Skip to Main Content

Author Details

Stacie K Loftus
National Human Genome Research Institute, National Institutes of Health
1993
52
28
PMIDPaper TitleJournal TitlePublished Year
37327787Haplotype-based analysis resolves missing heritability in oculocutaneous albinism type 1B.Am J Hum Genet2023
37327787Haplotype-based analysis resolves missing heritability in oculocutaneous albinism type 1B.Am J Hum Genet2023
34361043Computational Investigation of the pH Dependence of Stability of Melanosome Proteins: Implication for Melanosome formation and Disease.Int J Mol Sci2021
34246199A custom capture sequence approach for oculocutaneous albinism identifies structural variant alleles at the OCA2 locus.Hum Mutat2021
34361043Computational Investigation of the pH Dependence of Stability of Melanosome Proteins: Implication for Melanosome formation and Disease.Int J Mol Sci2021
34246199A custom capture sequence approach for oculocutaneous albinism identifies structural variant alleles at the OCA2 locus.Hum Mutat2021
30339321A curated gene list for expanding the horizons of pigmentation biology.Pigment Cell Melanoma Res2019
30339321A curated gene list for expanding the horizons of pigmentation biology.Pigment Cell Melanoma Res2019
31399133MEK inhibition remodels the active chromatin landscape and induces SOX10 genomic recruitment in BRAF(V600E) mutant melanoma cells.Epigenetics Chromatin2019
31315583Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations.BMC Genet2019
31315583Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations.BMC Genet2019
31399133MEK inhibition remodels the active chromatin landscape and induces SOX10 genomic recruitment in BRAF(V600E) mutant melanoma cells.Epigenetics Chromatin2019
29315345Identification and functional analysis of SOX10 phosphorylation sites in melanoma.PLoS One2018
30333196Cell-type-specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes.Genome Res2018
29337423The next generation of melanocyte data: Genetic, epigenetic, and transcriptional resource datasets and analysis tools.Pigment Cell Melanoma Res2018
29315345Identification and functional analysis of SOX10 phosphorylation sites in melanoma.PLoS One2018
30333196Cell-type-specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes.Genome Res2018
29337423The next generation of melanocyte data: Genetic, epigenetic, and transcriptional resource datasets and analysis tools.Pigment Cell Melanoma Res2018
29025994Loci associated with skin pigmentation identified in African populations.Science2017
29025994Loci associated with skin pigmentation identified in African populations.Science2017
28249010TFAP2 paralogs regulate melanocyte differentiation in parallel with MITF.PLoS Genet2017
28168807Hypoxia-induced HIF1α targets in melanocytes reveal a molecular profile associated with poor melanoma prognosis.Pigment Cell Melanoma Res2017
28168807Hypoxia-induced HIF1α targets in melanocytes reveal a molecular profile associated with poor melanoma prognosis.Pigment Cell Melanoma Res2017
28249010TFAP2 paralogs regulate melanocyte differentiation in parallel with MITF.PLoS Genet2017
26206884Genomic analysis reveals distinct mechanisms and functional classes of SOX10-regulated genes in melanocytes.Hum Mol Genet2015
26206884Genomic analysis reveals distinct mechanisms and functional classes of SOX10-regulated genes in melanocytes.Hum Mol Genet2015
24767210Distinct microRNA expression signatures are associated with melanoma subtypes and are regulated by HIF1A.Pigment Cell Melanoma Res2014
24767210Distinct microRNA expression signatures are associated with melanoma subtypes and are regulated by HIF1A.Pigment Cell Melanoma Res2014
23387001Decreased melanoma proliferation and cell survival: turn down your SOX10.Pigment Cell Melanoma Res2013
23913827SOX10 ablation arrests cell cycle, induces senescence, and suppresses melanomagenesis.Cancer Res2013
24267888A polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathway.Cell2013
23387001Decreased melanoma proliferation and cell survival: turn down your SOX10.Pigment Cell Melanoma Res2013
24267888A polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathway.Cell2013
23913827SOX10 ablation arrests cell cycle, induces senescence, and suppresses melanomagenesis.Cancer Res2013
23019145Integration of ChIP-seq and machine learning reveals enhancers and a predictive regulatory sequence vocabulary in melanocytes.Genome Res2012
23019145Integration of ChIP-seq and machine learning reveals enhancers and a predictive regulatory sequence vocabulary in melanocytes.Genome Res2012
21292980The pleiotropic mouse phenotype extra-toes spotting is caused by translation initiation factor Eif3c mutations and is associated with disrupted sonic hedgehog signaling.FASEB J2011
21292980The pleiotropic mouse phenotype extra-toes spotting is caused by translation initiation factor Eif3c mutations and is associated with disrupted sonic hedgehog signaling.FASEB J2011
21672228SOX10 directly modulates ERBB3 transcription via an intronic neural crest enhancer.BMC Dev Biol2011
21672228SOX10 directly modulates ERBB3 transcription via an intronic neural crest enhancer.BMC Dev Biol2011
20444197Sox proteins in melanocyte development and melanoma.Pigment Cell Melanoma Res2010
20451169Massively parallel sequencing of exons on the X chromosome identifies RBM10 as the gene that causes a syndromic form of cleft palate.Am J Hum Genet2010
20444197Sox proteins in melanocyte development and melanoma.Pigment Cell Melanoma Res2010
20451169Massively parallel sequencing of exons on the X chromosome identifies RBM10 as the gene that causes a syndromic form of cleft palate.Am J Hum Genet2010
18983539Gpnmb is a melanoblast-expressed, MITF-dependent gene.Pigment Cell Melanoma Res2009
19493314Comparison of melanoblast expression patterns identifies distinct classes of genes.Pigment Cell Melanoma Res2009
19422606Frequent mutations in the MITF pathway in melanoma.Pigment Cell Melanoma Res2009
19830815Oligodendroglial and pan-neural crest expression of Cre recombinase directed by Sox10 enhancer.Genesis2009
20161540Networks and pathways in pigmentation, health, and disease.Wiley Interdiscip Rev Syst Biol Med2009
18983539Gpnmb is a melanoblast-expressed, MITF-dependent gene.Pigment Cell Melanoma Res2009
  • 1 - 50 of 104

Recommended Authors

Institute of Anatomy, University of Zurich
Career Start Year 2009
Number of shared co-authors 11
National Human Genome Research Institute, National Institutes of Health
Career Start Year 2003
Number of shared co-authors 8
The Barcelona Institute of Science and Technology
Career Start Year 2003
Number of shared co-authors 0
the University of Iowa Carver College of Medicine
Career Start Year 2000
Number of shared co-authors 1
The Ohio State University
Career Start Year 2000
Number of shared co-authors 1
Amsterdam University Medical Centers location AMC
Career Start Year 1999
Number of shared co-authors 0
University of Iowa
Career Start Year 1999
Number of shared co-authors 0
McGill University and Genome Quebec Innovation Centre
Career Start Year 1998
Number of shared co-authors 3
Northwestern University
Career Start Year 1995
Number of shared co-authors 9
Max Planck Institute for Molecular Genetics
Career Start Year 1992
Number of shared co-authors 0
Ontario Institute for Cancer Research
Career Start Year 1991
Number of shared co-authors 9
National Human Genome Research Institute
Career Start Year 1990
Number of shared co-authors 17
The University of Melbourne
Career Start Year 1990
Number of shared co-authors 4
Broad Institute of Harvard and MIT
Career Start Year 1990
Number of shared co-authors 0
University of Maryland School of Medicine
Career Start Year 1989
Number of shared co-authors 7
Intractable Disease Research Center, Graduate School of Medicine, Juntendo University
Career Start Year 1989
Number of shared co-authors 5
Yale School of Medicine
Career Start Year 1989
Number of shared co-authors 3
McGill University
Career Start Year 1986
Number of shared co-authors 1
The University of Queensland Diamantina Institute, The University of Queensland
Career Start Year 1985
Number of shared co-authors 1
Kennedy Krieger Institute, Johns Hopkins University School of Medicine
Career Start Year 1984
Number of shared co-authors 1
Institute of Genetics and Cancer, The University of Edinburgh MRC Human Genetics Unit
Career Start Year 1984
Number of shared co-authors 3
National Institutes of Health
Career Start Year 1983
Number of shared co-authors 14
Marshfield Clinic Research Institute
Career Start Year 1983
Number of shared co-authors 4
Mayo Clinic
Career Start Year 1981
Number of shared co-authors 5
Carver College of Medicine, University of Iowa
Career Start Year 1980
Number of shared co-authors 4
Wellcome Sanger Institute
Career Start Year 1980
Number of shared co-authors 11
National Cancer Institute
Career Start Year 1980
Number of shared co-authors 8
HudsonAlpha Institute for Biotechnology, Stanford University
Career Start Year 1977
Number of shared co-authors 5
Invitae Corporation
Career Start Year 1976
Number of shared co-authors 8
Cincinnati Children's Hospital Medical Center
Career Start Year 1975
Number of shared co-authors 0

Collaborators

National Human Genome Research Institute, National Institutes of Health
Co-authored papers 39
Co-authored papers 15
Johns Hopkins University School of Medicine
Co-authored papers 7
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 6
Center for Epigenomics, University of California San Diego
Co-authored papers 5
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 3
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 3
Zhujiang Hospital, Southern Medical University
Co-authored papers 3
Co-authored papers 3
Technical University of Denmark
Co-authored papers 2
Center for Cancer Research, National Cancer Institute, National Institutes of Health
Co-authored papers 2
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 2
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 2
Ontario Institute for Cancer Research
Co-authored papers 2
University of Iowa
Co-authored papers 2
College of Dentistry & Dental Clinics, University of Iowa
Co-authored papers 2
Frazer Institute, The University of Queensland, Dermatology Research Centre
Co-authored papers 1
University of California San Diego
Co-authored papers 1
Moores Cancer Center, University of California
Co-authored papers 1
National Cancer Institute, National Institutes of Health
Co-authored papers 1
Co-authored papers 1
Weizmann Institute of Science
Co-authored papers 1
National Cancer Institute, National Institutes of Health
Co-authored papers 1
Co-authored papers 1
Center for Genomic and Computational Biology, Duke University Medical Center
Co-authored papers 1
National Human Genome Research Institute
Co-authored papers 1
University of Iceland
Co-authored papers 1
Center for Genomic & Computational Biology, Duke University
Co-authored papers 1
Center for Precision Health Research, National Human Genome Research Institute
Co-authored papers 1
Queensland Institute of Medical Research
Co-authored papers 1