Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans by Buonocore, Federica, Kühnen, Peter, Suntharalingham, Jenifer P, Del Valle, Ignacio, Digweed, Martin, Stachelscheid, Harald, Khajavi, Noushafarin, Didi, Mohammed, Brady, Angela F, Blankenstein, Oliver, Procter, Annie M, Dimitri, Paul, Wales, Jerry K H, Ghirri, Paolo, Knöbl, Dieter, Strahm, Brigitte, Erlacher, Miriam, Wlodarski, Marcin W, Chen, Wei, Kokai, George K, Anderson, Glenn, Morrogh, Deborah, Moulding, Dale A, McKee, Shane A, Niemeyer, Charlotte M, Grüters, Annette, Achermann, John C

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Human growth hormone 1 (GH1) gene expression: Complex haplotype‐dependent influence of polymorphic variation in the proximal promoter and locus control region by Horan, Martin, Millar, David S., Hedderich, Jürgen, Lewis, Geraint, Newsway, Vicky, Mo, Neil, Fryklund, Linda, Procter, Annie M., Krawczak, Michael, Cooper, David N.

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Beyond Loss: Dementia, Identity, Personhood by Procter, Annie M

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Novel mutations of the growth hormone 1 (GH1) gene disclosed by modulation of the clinical selection criteria for individuals with short stature by Millar, David S., Lewis, Mark D., Horan, Martin, Newsway, Vicky, Easter, Tammy E., Gregory, John W., Fryklund, Linda, Norin, Martin, Crowne, Elizabeth C., Davies, Sally J., Edwards, Phillip, Kirk, Jeremy, Waldron, Kim, Smith, Patricia J., Phillips III, John A., Scanlon, Maurice F., Krawczak, Michael, Cooper, David N., Procter, Annie M.

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Improving service delivery by evaluation of the referral pattern and capacity in a clinical genetics setting by McCann, Emma, Baines, Elizabeth A., Gray, Jonathon R., Procter, Annie M.

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Genetic variation at the growth hormone (GH1) and growth hormone receptor (GHR) loci as a risk factor for hypertension and stroke by HORAN, Martin, NEWSWAY, Vicky, HALL, Ian P, WHEATLEY, Amanda, BLAKEY, John, BATH, Philip M. W, COCKCROFT, John R, KRAWCZAK, Michael, COOPER, David N, LEWIS, Yasmin Mark D, EASTER, Tammy E, REES, D. Aled, MAHTO, Arti, MILLAR, David S, PROCTER, Annie M, SCANLON, Maurice F, WILKINSON, Ian B

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A Novel Dysfunctional Growth Hormone Variant (Ile179Met) Exhibits a Decreased Ability to Activate the Extracellular Signal-Regulated Kinase Pathway by Lewis, Mark D., Horan, Martin, Millar, David S., Newsway, Vicky, Easter, Tammy E., Fryklund, Linda, Gregory, John W., Norin, Martin, Del Valle, Cristóbal-Jorge, López-Siguero, Juan Pedro, Cañete, Ramón, López-Canti, Luis Fernando, Díaz-Torrado, Nieves, Espino, Rafael, Ulied, Angels, Scanlon, Maurice F., Procter, Annie M., Cooper, David N.

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Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans by Buonocore, Federica, Kuhnen, Peter, Suntharalingham, Jenifer P, Del Valle, Ignacio, Digweed, Martin, Stachelscheid, Harald, Khajavi, Noushafarin, Didi, Mohammed, Brady, Angela F, Blankenstein, Oliver, Procter, Annie M, Dimitri, Paul, Wales, Jerry K.H, Ghirri, Paolo, Knobl, Dieter, Strahm, Brigitte, Erlacher, Miriam, Wlodarski, Marcin W, Chen, Wei, Kokai, George K, Anderson, Glenn, Morrogh, Deborah, Moulding, Dale A, McKee, Shane A, Niemeyer, Charlotte M, Gruters, Annette, Achermann, John C

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Deformation of the palate in preterm infants by Procter, Annie M, Lether, Diane, Oliver, Richard G, Cartlidge, Patrick HT

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The molecular genetics of growth hormone deficiency by PROCTER, A. M, PHILLIPS, J. A, COOPER, D. N

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Improving Service Delivery by Evaluation of the Referral Pattern and Capacity in a Clinical Genetics Setting : Quality in clinical Genetics by MCCANN, Emma, BAINES, Elizabeth A, GRAY, Jonathon R, PROCTER, Annie M

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The ethics of genetic testing of families by Procter, Annie M

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Using high-resolution contact networks to evaluate SARS-CoV-2 transmission and control in large-scale multi-day events by Pung, Rachael, Firth, Josh A., Spurgin, Lewis G., Lee, Vernon J., Kucharski, Adam J.

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Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions by Chawner, Samuel J. R. A., Paine, Amy L., Dunn, Matt J., Walsh, Alice, Sloane, Poppy, Thomas, Megan, Evans, Alexandra, Hopkins‐Jones, Lucinda, Struik, Siske, Hall, Jeremy, Erichsen, Jonathan T., Leekam, Susan R., Owen, Michael J., Hay, Dale, Bree, Marianne B. M., Raymond, F. Lucy, Dewhurst, Eleanor, Lafont, Amy, Timur, Husniye, Wicks, Francesca, Ye, Zheng, Baker, Kate, Walker, Neil, Wallwork, Sarah, Skuse, David, Denaxas, Spiros, Mandy, William, Wolstencroft, Jeanne, Davies, Sarah, Erwood, Marie, Juj, Manoj, Kerry, Eleanor, Lucock, Anna, Printzlau, Frida, Srinivasan, Ramya, Walker, Susan, Coscini, Nadia, Fatih, Nasrtullah, Denyer, Hayley, Andrews, Sophie, Chawner, Samuel, Cuthbert, Andrew, Challenger, Aimee, Hall, Jeremy, Lewis, Nicola, Owen, Michael, Ray, Sinead, Sopp, Matthew, Moss, Hayley, Bree, Marianne, Holmans, Peter, Bowen, Samantha, Bradley, Karen, Birch, Philippa, Tong, Molly, Ford, Tasmin, Searle, Beverly, Wynn, Sarah, Robertson, Lisa, Berg, Jonathan, Lampe, Anne, Joss, Shelagh, Brennan, Paul, Kraus, Alison, Weber, Astrid, Rawson, Myfanwy, Quarrell, Oliver, Vasudevan, Pradeep, Harrison, Rachel, Williams, Denise, Maher, Eamonn, Kini, Usha, Clowes, Virginia, Van Dijk, Fleur, Gurasashvilli, Jana, Mansour, Sahar, Holder‐Espinasse, Muriel, Watford, Amy, Rankin, Julia, Baralle, Diana, Procter, Annie

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