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Dr. Steven Rauch Speaks at TEDx Kenmore Square

News: May 07, 2019

Harvard Medical School Professor of Otolaryngology–Head and Neck Surgery Steven D. Rauch, MD, was an invited speaker at last month’s TEDx Kenmore Square in Boston, Massachusetts. TED is a nonprofit organization that's devoted to spreading ideas, usually in the form of short, powerful talks on topics...

Sequencing Development Workshop

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The goal of the Sequencing Development Workshops is to bring together scientists who have significant experience in next-generation sequencing method development and optimization to discuss new ideas and technical challenges with peers who can provide guidance and insight towards overcoming these...

Berner, Daniel, Ursula Hoja, Matthias Zenkel, James Julian Ross, Steffen Uebe, Daniela Paoli, Paolo Frezzotti, et al. 2019. “The Protective Variant Rs7173049 at LOXL1 Locus Impacts on Retinoic Acid Signaling Pathway in Pseudoexfoliation Syndrome”. Hum Mol Genet.

Stem cell-derived tissue-associated regulatory T cells suppress the activity of pathogenic cells in autoimmune diabetes

Publication: Journal Article

Haque, Mohammad, Fengyang Lei, Xiaofang Xiong, Jugal Kishore Das, Xingcong Ren, Deyu Fang, Shahram Salek-Ardakani, Jin-Ming Yang, and Jianxun Song. 2019. “Stem Cell-Derived Tissue-Associated Regulatory T Cells Suppress the Activity of Pathogenic Cells in Autoimmune Diabetes”. JCI Insight 4 (7).

Longitudinal Clinical Follow-up and Genetic Spectrum of Patients With Rod-Cone Dystrophy Associated With Mutations in PDE6A and PDE6B

Publication: Journal Article

Khateb, Samer, Marco Nassisi, Kinga Bujakowska, Cécile Méjécase, Christel Condroyer, Aline Antonio, Marine Foussard, et al. 2019. “Longitudinal Clinical Follow-up and Genetic Spectrum of Patients With Rod-Cone Dystrophy Associated With Mutations in PDE6A and PDE6B”. JAMA Ophthalmol.

ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder

Publication: Journal Article

Williams, Lloyd, Asif Javed, Amin Sabri, Denise Morgan, Chad Huff, John Grigg, Xiu Ting Heng, et al. 2019. “ALPK1 Missense Pathogenic Variant in Five Families Leads to ROSAH Syndrome, an Ocular Multisystem Autosomal Dominant Disorder”. Genet Med 21 (9): 2103-15.

Monocanalicular Stents in Eyelid Lacerations: A Report by the American Academy of Ophthalmology

Publication: Journal Article

Wladis, Edward, Vinay Aakalu, Jeremiah Tao, Rachel Sobel, Suzanne Freitag, Jill Foster, and Louise Mawn. 2019. “Monocanalicular Stents in Eyelid Lacerations: A Report by the American Academy of Ophthalmology”. Ophthalmology 126 (9): 1324-29.

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Dr. Steven Rauch Speaks at TEDx Kenmore Square

Sequencing Development Workshop

FoxO Transcription Factors Are Critical Regulators of Diabetes-Related Muscle Atrophy.

FoxK1 and FoxK2 in insulin regulation of cellular and mitochondrial metabolism.

Developmental and functional heterogeneity of white adipocytes within a single fat depot.

The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome

Stem cell-derived tissue-associated regulatory T cells suppress the activity of pathogenic cells in autoimmune diabetes

Longitudinal Clinical Follow-up and Genetic Spectrum of Patients With Rod-Cone Dystrophy Associated With Mutations in PDE6A and PDE6B

ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder

Monocanalicular Stents in Eyelid Lacerations: A Report by the American Academy of Ophthalmology