Publications by authors named "Shenghui Duan"

23Publications

High bone mass from mutation of low-density lipoprotein receptor-related protein 6 (LRP6).

Bone 2020 Jul 27;141:115550. Epub 2020 Jul 27.

Center for Metabolic Bone Disease and Molecular Research, Shriners Hospitals for Children, St. Louis, MO, USA; Division of Bone and Mineral Diseases, Department of Internal Medicine, Washington University School of Medicine at Barnes-Jewish Hospital, St. Louis, MO, USA. Electronic address:

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http://dx.doi.org/10.1016/j.bone.2020.115550DOI Listing
July 2020

Juvenile Paget's Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor SP7).

Bone 2020 Aug 13;137:115364. Epub 2020 Apr 13.

Center For Metabolic Bone Disease and Molecular Research, Shriners Hospitals for Children - St. Louis, St. Louis, MO 63110, USA; Division of Bone and Mineral Diseases, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address:

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http://dx.doi.org/10.1016/j.bone.2020.115364DOI Listing
August 2020

Early-onset Paget's disease of bone in a Mexican family caused by a novel tandem duplication (77dup27) in TNFRSF11A that encodes RANK.

Bone 2020 04 8;133:115224. Epub 2020 Jan 8.

Division of Bone and Mineral Diseases, Department of Internal Medicine, Washington University School of Medicine at Barnes-Jewish Hospital, St. Louis, MO, USA; Center for Metabolic Bone Disease and Molecular Research, Shriners Hospitals for Children-St. Louis, St. Louis, MO, USA. Electronic address:

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http://dx.doi.org/10.1016/j.bone.2020.115224DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7179970PMC
April 2020

Hypophosphatemic osteosclerosis, hyperostosis, and enthesopathy associated with novel homozygous mutations of DMP1 encoding dentin matrix protein 1 and SPP1 encoding osteopontin: The first digenic SIBLING protein osteopathy?

Bone 2020 03 13;132:115190. Epub 2019 Dec 13.

Center for Metabolic Bone Disease and Molecular Research, Shriners Hospitals for Children - St. Louis, St. Louis, MO 63110, USA; Division of Bone and Mineral Diseases, Department of Internal Medicine, Washington University School of Medicine at Barnes-Jewish Hospital, St. Louis, MO 63110, USA. Electronic address:

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http://dx.doi.org/10.1016/j.bone.2019.115190DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7271119PMC
March 2020

New explanation for autosomal dominant high bone mass: Mutation of low-density lipoprotein receptor-related protein 6.

Bone 2019 10 11;127:228-243. Epub 2019 May 11.

Center for Metabolic Bone Disease and Molecular Research, Shriners Hospitals for Children - St. Louis, St. Louis, MO 63110, USA; Division of Bone and Mineral Diseases, Department of Internal Medicine, Washington University School of Medicine at Barnes-Jewish Hospital, St. Louis, MO 63110, USA. Electronic address:

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http://dx.doi.org/10.1016/j.bone.2019.05.003DOI Listing
October 2019

Sclerosteosis: Report of type 1 or 2 in three Indian Tamil families and literature review.

Bone 2018 11 2;116:321-332. Epub 2018 Aug 2.

Center for Metabolic Bone Disease and Molecular Research, Shriners Hospital for Children, St. Louis, MO 63110, USA; Division of Bone and Mineral Diseases, Department of Internal Medicine, Washington University School of Medicine at Barnes-Jewish Hospital, St. Louis, MO 63110, USA. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S87563282183029
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http://dx.doi.org/10.1016/j.bone.2018.07.022DOI Listing
November 2018

Raine Syndrome (OMIM #259775), Caused By FAM20C Mutation, Is Congenital Sclerosing Osteomalacia With Cerebral Calcification (OMIM 259660).

J Bone Miner Res 2017 04 14;32(4):757-769. Epub 2016 Dec 14.

Center for Metabolic Bone Disease and Molecular Research, Shriners Hospital for Children, St. Louis, MO, USA.

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http://dx.doi.org/10.1002/jbmr.3034DOI Listing
April 2017

Concentrations, diffusive fluxes and toxicity of heavy metals in pore water of the Fuyang River, Haihe Basin.

Ecotoxicol Environ Saf 2016 May 21;127:80-6. Epub 2016 Jan 21.

State Key Laboratory on Environmental Aquatic Chemistry, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 10085, China.

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http://dx.doi.org/10.1016/j.ecoenv.2016.01.013DOI Listing
May 2016

Multicentric carpotarsal osteolysis syndrome is caused by only a few domain-specific mutations in MAFB, a negative regulator of RANKL-induced osteoclastogenesis.

Am J Med Genet A 2014 Sep 2;164A(9):2287-93. Epub 2014 Jul 2.

Division of Bone and Mineral Diseases, Washington University School of Medicine at Barnes-Jewish Hospital, St. Louis, Missouri; Center for Metabolic Bone Disease and Molecular Research, Shriners Hospital for Children, St. Louis, Missouri.

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http://dx.doi.org/10.1002/ajmg.a.36641DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4505615PMC
September 2014

A subset of methylated CpG sites differentiate psoriatic from normal skin.

J Invest Dermatol 2012 Mar 10;132(3 Pt 1):583-92. Epub 2011 Nov 10.

Department of Genetics, Washington University School of Medicine, St Louis, Missouri 63110, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S0022202X1535640
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http://dx.doi.org/10.1038/jid.2011.348DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3568942PMC
March 2012

Frequent mutation of BAP1 in metastasizing uveal melanomas.

Science 2010 Dec 4;330(6009):1410-3. Epub 2010 Nov 4.

Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, MO 63110, USA.

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http://dx.doi.org/10.1126/science.1194472DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3087380PMC
December 2010

Oncogenic mutations in GNAQ occur early in uveal melanoma.

Invest Ophthalmol Vis Sci 2008 Dec 21;49(12):5230-4. Epub 2008 Aug 21.

Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, Missouri, USA.

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http://dx.doi.org/10.1167/iovs.08-2145DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2634606PMC
December 2008

Localization of PSORS1 to a haplotype block harboring HLA-C and distinct from corneodesmosin and HCR.

Hum Genet 2005 Dec 19;118(3-4):466-76. Epub 2005 Oct 19.

Department of Genetics, Washington University School of Medicine, Box 8232, 4566 Scott Avenue, St. Louis, Missouri, 63110, USA.

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http://link.springer.com/10.1007/s00439-005-0048-2
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http://dx.doi.org/10.1007/s00439-005-0048-2DOI Listing
December 2005

Efficient high-throughput resequencing of genomic DNA.

Genome Res 2003 Apr 12;13(4):717-20. Epub 2003 Mar 12.

Washington University, Division of Dermatology, St. Louis, Missouri 63110, USA.

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http://dx.doi.org/10.1101/gr.886203DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC430165PMC
April 2003

SNP discovery by direct DNA sequencing.

Methods Mol Biol 2003 ;212:71-84

Cardiovascular Research Institute, Department of Dermatology, University of California, San Francisco, San Francisco, CA, USA.

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http://dx.doi.org/10.1385/1-59259-327-5:071DOI Listing
May 2003

Novel immunoglobulin superfamily gene cluster, mapping to a region of human chromosome 17q25, linked to psoriasis susceptibility.

Hum Genet 2003 Jan 24;112(1):34-41. Epub 2002 Oct 24.

Departments of Genetics, Washington University School of Medicine, St. Louis, MO 63110, USA.

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http://dx.doi.org/10.1007/s00439-002-0851-yDOI Listing
January 2003

Replication of linkage of familial hypobetalipoproteinemia to chromosome 3p in six kindreds.

J Lipid Res 2002 Mar;43(3):407-15

Washington University School of Medicine, Department of Psychiatry, 660 South Euclid Avenue, Campus Box 8134, St. Louis, MO 63110, USA.

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March 2002