No Evidence for Parent of Origin Influencing Premature Ovarian Failure in Fragile X Premutation Carriers

Por Murray, Anna, Ennis, Sarah, Morton, Newton
Publicado em 2000

Nonlinear association between CGG repeat number and age of menopause in FMR1 premutation carriers

Por Ennis, Sarah, Ward, Daniel, Murray, Anna
Publicado em 2006

Age-Related Macular Degeneration: A Disease of Systemic or Local Complement Dysregulation?

Por Warwick, Alasdair, Khandhadia, Samir, Ennis, Sarah, Lotery, Andrew
Publicado no J Clin Med (2014)

Genome Scanning by Composite Likelihood

Por Morton, Newton, Maniatis, Nikolas, Zhang, Weihua, Ennis, Sarah, Collins, Andrew
Publicado em 2007

Fine‐scale linkage disequilibrium mapping of age‐related macular degeneration in the complement factor H gene region

Por Ennis, Sarah, Goverdhan, Srini, Cree, Angela, Hoh, Josephine, Collins, Andrew, Lotery, Andrew
Publicado em 2007

Support for the involvement of complement factor I in age-related macular degeneration

Por Ennis, Sarah, Gibson, Jane, Cree, Angela J, Collins, Andrew, Lotery, Andrew J
Publicado em 2010

Genome-wide association of breast cancer: composite likelihood with imputed genotypes

Por Politopoulos, Ioannis, Gibson, Jane, Tapper, William, Ennis, Sarah, Eccles, Diana, Collins, Andrew
Publicado em 2011

Reproductive and menstrual history of females with fragile X expansions

Por Murray, Anna, Ennis, Sarah, MacSwiney, Felicity, Webb, James, Morton, Newton E
Publicado em 2000

Complement factor I and age-related macular degeneration

Por Alexander, Philip, Gibson, Jane, Cree, Angela J., Ennis, Sarah, Lotery, Andrew J.
Publicado em 2014

Prospective study of Outcomes in Sporadic versus Hereditary breast cancer (POSH): study protocol

Por Ennis Sarah, Hammond Victoria, Simmonds Peter, Gerty Sue, Eccles Diana, Altman Douglas G
Publicado em 2007-08-01

Prospective study of Outcomes in Sporadic versus Hereditary breast cancer (POSH): study protocol

Por Eccles, Diana, Gerty, Sue, Simmonds, Peter, Hammond, Victoria, Ennis, Sarah, Altman, Douglas G
Publicado em 2007

Evaluating phenotype-driven approaches for genetic diagnoses from exomes in a clinical setting

Por Pengelly, Reuben J., Alom, Thahmina, Zhang, Zijian, Hunt, David, Ennis, Sarah, Collins, Andrew
Publicado no Sci Rep (2017)

The influence of genetic variation in 30 selected genes on the clinical characteristics of early onset breast cancer

Por Tapper, William, Hammond, Victoria, Gerty, Sue, Ennis, Sarah, Simmonds, Peter, Collins, Andrew, Eccles, Diana
Publicado em 2008

A SNP profiling panel for sample tracking in whole-exome sequencing studies

Por Pengelly, Reuben J, Gibson, Jane, Andreoletti, Gaia, Collins, Andrew, Mattocks, Christopher J, Ennis, Sarah
Publicado em 2013

Erratum to: a SNP profiling panel for sample tracking in whole-exome sequencing studies

Por Pengelly, Reuben J, Gibson, Jane, Andreoletti, Gaia, Collins, Andrew, Mattocks, Christopher J, Ennis, Sarah
Publicado no Genome Med (2015)

Support Vector Machine Classifier for Estrogen Receptor Positive and Negative Early-Onset Breast Cancer

Por Upstill-Goddard, Rosanna, Eccles, Diana, Ennis, Sarah, Rafiq, Sajjad, Tapper, William, Fliege, Joerg, Collins, Andrew
Publicado em 2013

Whole genome sequences are required to fully resolve the linkage disequilibrium structure of human populations

Por Pengelly, Reuben J., Tapper, William, Gibson, Jane, Knut, Marcin, Tearle, Rick, Collins, Andrew, Ennis, Sarah
Publicado no BMC Genomics (2015)

Progressive myoclonic epilepsy with Fanconi syndrome

Por Seaby, Eleanor G, Gilbert, Rodney D, Pengelly, Reuben J, Andreoletti, Gaia, Clarke, Antonia, Ennis, Sarah
Publicado no JRSM Open (2016)

Unexpected Findings in a Child with Atypical Hemolytic Uremic Syndrome: An Example of How Genomics Is Changing the Clinical Diagnostic Paradigm

Por Seaby, Eleanor G., Gilbert, Rodney D., Andreoletti, Gaia, Pengelly, Reuben J., Mercer, Catherine, Hunt, David, Ennis, Sarah
Publicado no Front Pediatr (2017)

AMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis

Por Andreoletti, Gaia, Seaby, Eleanor G, Dewing, Jennifer M, O'Kelly, Ita, Lachlan, Katherine, Gilbert, Rodney D, Ennis, Sarah
Publicado no J Med Genet (2017)