Patients' understanding of genetic susceptibility testing in mainstream medicine: qualitative study on thrombophilia

द्वारा Shepherd Maggie H, Richards Suzanne H, Ellard Sian, Saukko Paula M, Campbell John L
प्रकाशित 2007-06-01

Patients' understanding of genetic susceptibility testing in mainstream medicine: qualitative study on thrombophilia

द्वारा Saukko, Paula M, Ellard, Sian, Richards, Suzanne H, Shepherd, Maggie H, Campbell, John L
प्रकाशित 2007

GATA6 Mutations Cause a Broad Phenotypic Spectrum of Diabetes From Pancreatic Agenesis to Adult-Onset Diabetes Without Exocrine Insufficiency

द्वारा De Franco, Elisa, Shaw-Smith, Charles, Flanagan, Sarah E., Shepherd, Maggie H., Hattersley, Andrew T., Ellard, Sian
प्रकाशित 2013

Using highly sensitive C-reactive protein measurement to diagnose MODY in a family with suspected type 2 diabetes

द्वारा Besser, Rachel E J, Jones, Jackie, McDonald, Timothy J, Smith, Rebecca, Shepherd, Maggie H, Hattersley, Andrew T
प्रकाशित 2012

An engaged research study to assess the effect of a ‘real-world’ dietary intervention on urinary bisphenol A (BPA) levels in teenagers

द्वारा Galloway, Tamara S, Baglin, Nigel, Lee, Benjamin P, Kocur, Anna L, Shepherd, Maggie H, Steele, Anna M, Harries, Lorna W
में प्रकाशित BMJ Open (2018)

A UK nationwide prospective study of treatment change in MODY: genetic subtype and clinical characteristics predict optimal glycaemic control after discontinuing insulin and metfor...

द्वारा Shepherd, Maggie H., Shields, Beverley M., Hudson, Michelle, Pearson, Ewan R., Hyde, Christopher, Ellard, Sian, Hattersley, Andrew T., Patel, Kashyap A.
में प्रकाशित Diabetologia (2018)

Urinary C-Peptide Creatinine Ratio Is a Practical Outpatient Tool for Identifying Hepatocyte Nuclear Factor 1-α/Hepatocyte Nuclear Factor 4-α Maturity-Onset Diabetes of the Young F...

द्वारा Besser, Rachel E.J., Shepherd, Maggie H., McDonald, Timothy J., Shields, Beverley M., Knight, Bridget A., Ellard, Sian, Hattersley, Andrew T.
प्रकाशित 2011

Improvements in Awareness and Testing Have Led to a Threefold Increase Over 10 Years in the Identification of Monogenic Diabetes in the U.K.

द्वारा Pang, Lewis, Colclough, Kevin C., Shepherd, Maggie H., McLean, Joanne, Pearson, Ewan R., Ellard, Sian, Hattersley, Andrew T., Shields, Beverley M.
में प्रकाशित Diabetes Care (2022)

Transient Neonatal Diabetes: An Etiologic Clue for the Adult Diabetologist

द्वारा Novak, Anela, Bowman, Pamela, Kraljevic, Ivana, Tripolski, Marija, Houghton, Jayne A.L., De Franco, Elisa, Shepherd, Maggie H., Skrabic, Veselin, Patel, Kashyap A.
में प्रकाशित Can J Diabetes (2020)

Patient preference for second and third line therapies in type 2 diabetes: a prespecified secondary endpoint of the TriMaster study

द्वारा Shields, Beverley M, Angwin, Catherine D, Shepherd, Maggie H, Britten, Nicky, Jones, Angus G, Sattar, Naveed, Holman, Rury, Pearson, Ewan R, Hattersley, Andrew T
में प्रकाशित Nat Med (2023)

Screening for neonatal diabetes at day 5 of life using dried blood spot glucose measurement

द्वारा McDonald, Timothy J., Besser, Rachel E., Perry, Mandy, Babiker, Tarig, Knight, Bridget A., Shepherd, Maggie H., Ellard, Sian, Flanagan, Sarah E., Hattersley, Andrew T.
में प्रकाशित Diabetologia (2017)

Cognitive, neurological and behavioral features in adults with KCNJ11 neonatal diabetes

द्वारा Bowman, Pamela, Day, Jacob, Torrens, Lorna, Shepherd, Maggie H, Knight, Bridget A, Ford, Tamsin J, Flanagan, Sarah E, Chakera, Ali, Hattersley, Andrew T, Zeman, Adam
में प्रकाशित Diabetes Care (2018)

Noninvasive Fetal Genotyping by Droplet Digital PCR to Identify Maternally Inherited Monogenic Diabetes Variants

द्वारा Caswell, Richard C., Snowsill, Tristan, Houghton, Jayne A.L., Chakera, Ali J., Shepherd, Maggie H., Laver, Thomas W., Knight, Bridget A., Wright, David, Hattersley, Andrew T., Ellard, Sian
में प्रकाशित Clin Chem (2020)

Successful transfer to sulfonylureas in KCNJ11 neonatal diabetes is determined by the mutation and duration of diabetes

द्वारा Babiker, Tarig, Vedovato, Natascia, Patel, Kashyap, Thomas, Nicholas, Finn, Roisin, Männikkö, Roope, Chakera, Ali J., Flanagan, Sarah E., Shepherd, Maggie H., Ellard, Sian, Ashcroft, Frances M., Hattersley, Andrew T.
में प्रकाशित Diabetologia (2016)

GATA6 Cooperates with EOMES/SMAD2/3 to Deploy the Gene Regulatory Network Governing Human Definitive Endoderm and Pancreas Formation

द्वारा Chia, Crystal Y., Madrigal, Pedro, Denil, Simon L.I.J., Martinez, Iker, Garcia-Bernardo, Jose, El-Khairi, Ranna, Chhatriwala, Mariya, Shepherd, Maggie H., Hattersley, Andrew T., Dunn, N. Ray, Vallier, Ludovic
में प्रकाशित Stem Cell Reports (2019)

Patterns of postmeal insulin secretion in individuals with sulfonylurea-treated KCNJ11 neonatal diabetes show predominance of non-K(ATP)-channel pathways

द्वारा Bowman, Pamela, McDonald, Timothy J, Knight, Bridget A, Flanagan, Sarah E, Leveridge, Maria, Spaull, Steve R, Shields, Beverley M, Hammersley, Suzanne, Shepherd, Maggie H, Andrews, Robert C, Patel, Kashyap A, Hattersley, Andrew T
में प्रकाशित BMJ Open Diabetes Res Care (2019)

Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance

द्वारा Patel, Kashyap A., Kettunen, Jarno, Laakso, Markku, Stančáková, Alena, Laver, Thomas W., Colclough, Kevin, Johnson, Matthew B., Abramowicz, Marc, Groop, Leif, Miettinen, Päivi J., Shepherd, Maggie H., Flanagan, Sarah E., Ellard, Sian, Inagaki, Nobuya, Hattersley, Andrew T., Tuomi, Tiinamaija, Cnop, Miriam, Weedon, Michael N.
में प्रकाशित Nat Commun (2017)

Long-term Follow-up of Glycemic and Neurological Outcomes in an International Series of Patients With Sulfonylurea-Treated ABCC8 Permanent Neonatal Diabetes

द्वारा Bowman, Pamela, Mathews, Frances, Barbetti, Fabrizio, Shepherd, Maggie H., Sanchez, Janine, Piccini, Barbara, Beltrand, Jacques, Letourneau-Freiberg, Lisa R., Polak, Michel, Greeley, Siri Atma W., Rawlins, Eamon, Babiker, Tarig, Thomas, Nicholas J., De Franco, Elisa, Ellard, Sian, Flanagan, Sarah E., Hattersley, Andrew T.
में प्रकाशित Diabetes Care (2021)

Insulin Mutation Screening in 1044 Patients with Diabetes: Mutations in the INS gene are a Common Cause of Neonatal Diabetes but a Rare Cause of Diabetes Diagnosed in Childhood or...

द्वारा Edghill, Emma L., Flanagan, Sarah E., Patch, Ann-Marie, Boustred, Chris, Parrish, Andrew, Shields, Beverley, Shepherd, Maggie H., Hussain, Khalid, Kapoor, Ritika R., Malecki, Maciej, MacDonald, Michael J., Støy, Julie, Steiner, Donald F., Philipson, Louis H., Bell, Graeme I., Hattersley, Andrew T., Ellard, Sian
में प्रकाशित Diabetes (2008)

Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study

द्वारा Bowman, Pamela, Sulen, Åsta, Barbetti, Fabrizio, Beltrand, Jacques, Svalastoga, Pernille, Codner, Ethel, Tessmann, Ellen H, Juliusson, Petur B, Skrivarhaug, Torild, Pearson, Ewan R, Flanagan, Sarah E, Babiker, Tarig, Thomas, Nicholas J, Shepherd, Maggie H, Ellard, Sian, Klimes, Iwar, Szopa, Magdalena, Polak, Michel, Iafusco, Dario, Hattersley, Andrew T, Njølstad, Pål R
में प्रकाशित Lancet Diabetes Endocrinol (2018)