{"id":6,"date":"2018-07-23T14:21:11","date_gmt":"2018-07-23T14:21:11","guid":{"rendered":"https:\/\/lab.research.sickkids.ca\/yuen\/?page_id=6"},"modified":"2024-05-07T15:00:12","modified_gmt":"2024-05-07T15:00:12","slug":"research","status":"publish","type":"page","link":"https:\/\/lab.research.sickkids.ca\/yuen\/research\/","title":{"rendered":"Research"},"content":{"rendered":"<p><div class=\"fusion-fullwidth fullwidth-box fusion-builder-row-1 fusion-flex-container nonhundred-percent-fullwidth non-hundred-percent-height-scrolling\" style=\"--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-padding-top:20px;--awb-flex-wrap:wrap;\" ><div class=\"fusion-builder-row fusion-row fusion-flex-align-items-center fusion-flex-content-wrap\" style=\"max-width:1331.2px;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-0 fusion_builder_column_1_2 1_2 fusion-flex-column\" style=\"--awb-bg-blend:overlay;--awb-bg-size:cover;--awb-width-large:50%;--awb-margin-top-large:30px;--awb-spacing-right-large:3.84%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:3.84%;--awb-width-medium:100%;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-image-element \" style=\"--awb-caption-title-font-family:var(--h2_typography-font-family);--awb-caption-title-font-weight:var(--h2_typography-font-weight);--awb-caption-title-font-style:var(--h2_typography-font-style);--awb-caption-title-size:var(--h2_typography-font-size);--awb-caption-title-transform:var(--h2_typography-text-transform);--awb-caption-title-line-height:var(--h2_typography-line-height);--awb-caption-title-letter-spacing:var(--h2_typography-letter-spacing);\"><span class=\" fusion-imageframe imageframe-none imageframe-1 hover-type-none\"><img decoding=\"async\" width=\"943\" height=\"506\" alt=\"Diagram showing DNA with a tandem repeat detected in parent, and expanded in the child\" title=\"SickKids Tandem Repeat Expansion Figure\" src=\"https:\/\/lab.research.sickkids.ca\/yuen\/wp-content\/uploads\/sites\/101\/2020\/12\/Screen-Shot-2020-12-08-at-10.28.13-AM.png\" class=\"img-responsive wp-image-604\" srcset=\"https:\/\/lab.research.sickkids.ca\/yuen\/wp-content\/uploads\/sites\/101\/2020\/12\/Screen-Shot-2020-12-08-at-10.28.13-AM-200x107.png 200w, https:\/\/lab.research.sickkids.ca\/yuen\/wp-content\/uploads\/sites\/101\/2020\/12\/Screen-Shot-2020-12-08-at-10.28.13-AM-400x215.png 400w, https:\/\/lab.research.sickkids.ca\/yuen\/wp-content\/uploads\/sites\/101\/2020\/12\/Screen-Shot-2020-12-08-at-10.28.13-AM-600x322.png 600w, https:\/\/lab.research.sickkids.ca\/yuen\/wp-content\/uploads\/sites\/101\/2020\/12\/Screen-Shot-2020-12-08-at-10.28.13-AM-800x429.png 800w, https:\/\/lab.research.sickkids.ca\/yuen\/wp-content\/uploads\/sites\/101\/2020\/12\/Screen-Shot-2020-12-08-at-10.28.13-AM.png 943w\" sizes=\"(max-width: 1024px) 100vw, (max-width: 640px) 100vw, 800px\" \/><\/span><\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-1 fusion_builder_column_1_2 1_2 fusion-flex-column\" style=\"--awb-bg-blend:overlay;--awb-bg-size:cover;--awb-width-large:50%;--awb-margin-top-large:0px;--awb-spacing-right-large:3.84%;--awb-margin-bottom-large:0px;--awb-spacing-left-large:3.84%;--awb-width-medium:100%;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-flex-justify-content-center fusion-content-layout-column\"><div class=\"fusion-text fusion-text-1\"><h2>Tandem Repeat Expansions<\/h2>\n<p>Tandem repeats (TRs) are a class of DNA sequence where two or more bases are repeated immediately adjacent to one another. Expansions of these repetitive regions are suspected to contribute to the genetic etiology of complex disorders.<\/p>\n<p>Short-read whole-genome sequencing (WGS) has trouble characterizing these regions due to ambiguous mapping. We are developing and implementing new technologies and computational algorithms to perform genome-wide screens of repetitive DNA. Our aims are to genotype TRs on large genomic datasets as well as determine the role, and characterize the mechanism, of TR variation.<\/p>\n<\/div><\/div><\/div><\/div><\/div><div class=\"fusion-fullwidth fullwidth-box fusion-builder-row-2 fusion-flex-container nonhundred-percent-fullwidth non-hundred-percent-height-scrolling\" style=\"--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-margin-top:50px;--awb-flex-wrap:wrap;\" ><div class=\"fusion-builder-row fusion-row fusion-flex-align-items-center fusion-flex-content-wrap\" style=\"max-width:1331.2px;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-2 fusion_builder_column_1_2 1_2 fusion-flex-column\" style=\"--awb-bg-blend:overlay;--awb-bg-size:cover;--awb-width-large:50%;--awb-margin-top-large:0px;--awb-spacing-right-large:3.84%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:3.84%;--awb-width-medium:100%;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-image-element \" style=\"text-align:center;--awb-caption-title-font-family:var(--h2_typography-font-family);--awb-caption-title-font-weight:var(--h2_typography-font-weight);--awb-caption-title-font-style:var(--h2_typography-font-style);--awb-caption-title-size:var(--h2_typography-font-size);--awb-caption-title-transform:var(--h2_typography-text-transform);--awb-caption-title-line-height:var(--h2_typography-line-height);--awb-caption-title-letter-spacing:var(--h2_typography-letter-spacing);\"><span class=\" fusion-imageframe imageframe-none imageframe-2 hover-type-none\"><img decoding=\"async\" width=\"279\" height=\"300\" alt=\"blue cartoon brain\" title=\"Open soure blue cartoon brain\" src=\"https:\/\/lab.research.sickkids.ca\/yuen\/wp-content\/uploads\/sites\/101\/2020\/12\/brain-1710293_1280-279x300.png\" class=\"img-responsive wp-image-607\" srcset=\"https:\/\/lab.research.sickkids.ca\/yuen\/wp-content\/uploads\/sites\/101\/2020\/12\/brain-1710293_1280-200x215.png 200w, https:\/\/lab.research.sickkids.ca\/yuen\/wp-content\/uploads\/sites\/101\/2020\/12\/brain-1710293_1280-400x430.png 400w, https:\/\/lab.research.sickkids.ca\/yuen\/wp-content\/uploads\/sites\/101\/2020\/12\/brain-1710293_1280-600x645.png 600w, https:\/\/lab.research.sickkids.ca\/yuen\/wp-content\/uploads\/sites\/101\/2020\/12\/brain-1710293_1280-800x861.png 800w, https:\/\/lab.research.sickkids.ca\/yuen\/wp-content\/uploads\/sites\/101\/2020\/12\/brain-1710293_1280.png 1190w\" sizes=\"(max-width: 1024px) 100vw, (max-width: 640px) 100vw, 800px\" \/><\/span><\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-3 fusion_builder_column_1_2 1_2 fusion-flex-column\" style=\"--awb-bg-blend:overlay;--awb-bg-size:cover;--awb-width-large:50%;--awb-margin-top-large:0px;--awb-spacing-right-large:3.84%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:3.84%;--awb-width-medium:100%;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-text fusion-text-2\"><h2>\u200bWhole Genome Sequencing Analysis of Neurological Disorders<\/h2>\n<p>Many neurological disorders have a complex genetic origin, meaning the same, single gene cannot explain the phenotype for most cases. We carry out WGS analysis to investigate different forms of rare genetic (including single nucleotide, copy number, and TR) variation in neurological disorders, such as autism spectrum disorder, movement disorders, epilepsy, and schizophrenia.<\/p>\n<h3>Participate in our research!<\/h3>\n<p>We are actively recruiting participants with unexplained pediatric-onset movement disorders for a whole genome sequencing study. Check out our study poster or expand the section below to learn more.<\/p>\n<\/div><div class=\"accordian fusion-accordian\" style=\"--awb-border-size:1px;--awb-icon-size:13px;--awb-content-font-size:16px;--awb-icon-alignment:left;--awb-hover-color:#f9f9f9;--awb-border-color:#cccccc;--awb-background-color:#ffffff;--awb-divider-color:#e0dede;--awb-divider-hover-color:#e0dede;--awb-icon-color:#ffffff;--awb-title-color:#0046ad;--awb-content-color:#0a0a0a;--awb-icon-box-color:#333333;--awb-toggle-hover-accent-color:#00afd8;--awb-title-font-family:&quot;Lato&quot;;--awb-title-font-weight:400;--awb-title-font-style:normal;--awb-title-font-size:13px;--awb-title-line-height:1.36;--awb-content-font-family:Arial, Helvetica, sans-serif;--awb-content-font-style:normal;--awb-content-font-weight:400;\"><div class=\"panel-group fusion-toggle-icon-boxed\" id=\"accordion-6-1\"><div class=\"fusion-panel panel-default panel-bbb9f459f32027014 fusion-toggle-has-divider\" style=\"--awb-title-color:#0046ad;--awb-content-color:#0a0a0a;\"><div class=\"panel-heading\"><h4 class=\"panel-title toggle\" id=\"toggle_bbb9f459f32027014\"><a aria-expanded=\"false\" aria-controls=\"bbb9f459f32027014\" role=\"button\" data-toggle=\"collapse\" data-parent=\"#accordion-6-1\" data-target=\"#bbb9f459f32027014\" href=\"#bbb9f459f32027014\"><span class=\"fusion-toggle-icon-wrapper\" aria-hidden=\"true\"><i class=\"fa-fusion-box active-icon awb-icon-minus\" aria-hidden=\"true\"><\/i><i class=\"fa-fusion-box inactive-icon awb-icon-plus\" aria-hidden=\"true\"><\/i><\/span><span class=\"fusion-toggle-heading\">Learn more about this study<\/span><\/a><\/h4><\/div><div id=\"bbb9f459f32027014\" class=\"panel-collapse collapse \" aria-labelledby=\"toggle_bbb9f459f32027014\"><div class=\"panel-body toggle-content fusion-clearfix\">\n<p data-fontsize=\"16\" data-lineheight=\"24px\">Do you or your child have a childhood-onset movement disorder with no known cause?<\/p>\n<p data-fontsize=\"16\" data-lineheight=\"24px\">In this study, we will look at your DNA to try and find an explanation for the disorder.<\/p>\n<p data-fontsize=\"16\" data-lineheight=\"24px\"><strong>What is involved?<\/strong><\/p>\n<p data-fontsize=\"16\" data-lineheight=\"24px\">A blood draw, saliva sample or cheek swab to get your DNA.<\/p>\n<p data-fontsize=\"16\" data-lineheight=\"24px\">If you are interested in learning more and\/or taking part in this study, please contact Phoenix Doong at <span style=\"text-decoration: underline\"><a href=\"mailto:hoilam.doong@sickkids.ca\">hoilam.doong@sickkids.ca<\/a><\/span> or 416-813-7654 ext. 309663<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><div class=\"fusion-fullwidth fullwidth-box fusion-builder-row-3 fusion-flex-container nonhundred-percent-fullwidth non-hundred-percent-height-scrolling\" style=\"--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-margin-top:50px;--awb-flex-wrap:wrap;\" ><div class=\"fusion-builder-row fusion-row fusion-flex-align-items-center fusion-flex-content-wrap\" style=\"max-width:1331.2px;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-4 fusion_builder_column_1_2 1_2 fusion-flex-column\" style=\"--awb-bg-blend:overlay;--awb-bg-size:cover;--awb-width-large:50%;--awb-margin-top-large:0px;--awb-spacing-right-large:3.84%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:3.84%;--awb-width-medium:100%;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-image-element \" style=\"text-align:center;--awb-caption-title-font-family:var(--h2_typography-font-family);--awb-caption-title-font-weight:var(--h2_typography-font-weight);--awb-caption-title-font-style:var(--h2_typography-font-style);--awb-caption-title-size:var(--h2_typography-font-size);--awb-caption-title-transform:var(--h2_typography-text-transform);--awb-caption-title-line-height:var(--h2_typography-line-height);--awb-caption-title-letter-spacing:var(--h2_typography-letter-spacing);\"><span class=\" fusion-imageframe imageframe-none imageframe-3 hover-type-none\"><img decoding=\"async\" width=\"300\" height=\"294\" alt=\"2 diagrams: one showing a section of a chromosome being duplicated, the second showing the same duplication with x&#039;s on other parts of the chromosome to indicate genetic modifiers\" title=\"Genetic Modifier Diagram\" src=\"https:\/\/lab.research.sickkids.ca\/yuen\/wp-content\/uploads\/sites\/101\/2020\/12\/Genetic-Modifier-Diagram-300x294.png\" class=\"img-responsive wp-image-617\" srcset=\"https:\/\/lab.research.sickkids.ca\/yuen\/wp-content\/uploads\/sites\/101\/2020\/12\/Genetic-Modifier-Diagram-200x196.png 200w, https:\/\/lab.research.sickkids.ca\/yuen\/wp-content\/uploads\/sites\/101\/2020\/12\/Genetic-Modifier-Diagram-400x392.png 400w, https:\/\/lab.research.sickkids.ca\/yuen\/wp-content\/uploads\/sites\/101\/2020\/12\/Genetic-Modifier-Diagram.png 595w\" sizes=\"(max-width: 1024px) 100vw, (max-width: 640px) 100vw, 300px\" \/><\/span><\/div><\/div><\/div><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-5 fusion_builder_column_1_2 1_2 fusion-flex-column\" style=\"--awb-bg-blend:overlay;--awb-bg-size:cover;--awb-width-large:50%;--awb-margin-top-large:0px;--awb-spacing-right-large:3.84%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:3.84%;--awb-width-medium:100%;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-text fusion-text-3\"><h2><span style=\"color: #000000\">Genetic Modifiers<\/span><\/h2>\n<p>Pathogenic genetic variants often exhibit incomplete penetrance and variable expressivity. Additional genetic factors (e.g., single nucleotide variants, copy number variants, structural variants, and TR expansions), which may act as modifiers, are sometimes present in affected individuals. We are studying this phenomenon in a number of disorders, including the 7q11.23 duplication syndrome, the 22q11.2 deletion syndrome, and in TR expansion related diseases such as motor neuron disease.<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/p>\n","protected":false},"excerpt":{"rendered":"","protected":false},"author":229,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-6","page","type-page","status-publish","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v27.0 (Yoast SEO v27.0) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>Research - Yuen Lab<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/lab.research.sickkids.ca\/yuen\/research\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Research\" \/>\n<meta property=\"og:url\" content=\"https:\/\/lab.research.sickkids.ca\/yuen\/research\/\" \/>\n<meta property=\"og:site_name\" content=\"Yuen Lab\" \/>\n<meta property=\"article:modified_time\" content=\"2024-05-07T15:00:12+00:00\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"7 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/lab.research.sickkids.ca\/yuen\/research\/\",\"url\":\"https:\/\/lab.research.sickkids.ca\/yuen\/research\/\",\"name\":\"Research - 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