PUBLICATIONS

MITOCHONDRIA

GENETICS

CHOLESTEROL EFFLUX

Publications

We are continually updating our lists of publications.

Please click on the corresponding publications listed below for further information.

<img alt="" data-src="https://religendx.com/wp-content/uploads/2019/07/images.png" class="et-waypoint et_pb_animation_top lazyload" src="data:image/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==" /><noscript><img alt="" data-src="https://religendx.com/wp-content/uploads/2019/07/images.png" class="et-waypoint et_pb_animation_top lazyload" src="data:image/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==" /><noscript><img src="https://religendx.com/wp-content/uploads/2019/07/images.png" alt="" class="et-waypoint et_pb_animation_top" />

A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders

<img alt="" data-src="https://religendx.com/wp-content/uploads/2019/07/images.png" class="et-waypoint et_pb_animation_top lazyload" src="data:image/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==" /><noscript><img alt="" data-src="https://religendx.com/wp-content/uploads/2019/07/images.png" class="et-waypoint et_pb_animation_top lazyload" src="data:image/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==" /><noscript><img src="https://religendx.com/wp-content/uploads/2019/07/images.png" alt="" class="et-waypoint et_pb_animation_top" />

A clinical utility study of exome sequencing versus conventional genetic testing in pediatric neurology

<img alt="" data-src="https://religendx.com/wp-content/uploads/2019/07/images.png" class="et-waypoint et_pb_animation_top lazyload" src="data:image/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==" /><noscript><img alt="" data-src="https://religendx.com/wp-content/uploads/2019/07/images.png" class="et-waypoint et_pb_animation_top lazyload" src="data:image/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==" /><noscript><img src="https://religendx.com/wp-content/uploads/2019/07/images.png" alt="" class="et-waypoint et_pb_animation_top" />

Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test

<img alt="" data-src="https://religendx.com/wp-content/uploads/2019/07/images.png" class="et-waypoint et_pb_animation_top lazyload" src="data:image/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==" /><noscript><img alt="" data-src="https://religendx.com/wp-content/uploads/2019/07/images.png" class="et-waypoint et_pb_animation_top lazyload" src="data:image/gif;base64,R0lGODlhAQABAAAAACH5BAEKAAEALAAAAAABAAEAAAICTAEAOw==" /><noscript><img src="https://religendx.com/wp-content/uploads/2019/07/images.png" alt="" class="et-waypoint et_pb_animation_top" />

Genome sequencing and implications for rare disorders

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