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1

PhantasiaâThe psychological significance of lifelong visual imagery vividness extremes

Zeman, Adam, Milton, Fraser, Della Sala, Sergio, Dewar, Michaela, Frayling, Timothy, Gaddum, James, Hattersley, Andrew, Heuerman-Williamson, Brittany, Jones, Kealan, MacKisack, Matthew, Winlove, Crawf

Journal:

Year:

2020

File:

PDF, 1.81 MB

2020

2

ISPAD Clinical Practice Consensus Guidelines 2018: The diagnosis and management of monogenic diabetes in children and adolescents

Hattersley, Andrew T., Greeley, Siri A. W., Polak, Michel, Rubio-Cabezas, Oscar, Njølstad, Pål R., Mlynarski, Wojciech, Castano, Luis, Carlsson, Annelie, Raile, Klemens, Chi, Dung V., Ellard, Sian, Cr

Journal:

Pediatric Diabetes

Year:

2018

Language:

english

File:

PDF, 1.34 MB

english, 2018

3

Extreme phenotypic diversity and nonpenetrance in families with the LMNA gene mutation R644C

Julia Rankin, Michaela Auer-Grumbach, Warwick Bagg, Kevin Colclough, Nguyen Thuy Duong, Jane Fenton-May, Andrew Hattersley, Judith Hudson, Philip Jardine, Dragana Josifova, Cheryl Longman, Robert McWi

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 270 KB

english, 2008

4

The diagnosis and management of monogenic diabetes in children and adolescents

Andrew Hattersley, Jan Bruining, Julian Shield, Pal Njolstad, Kim C Donaghue

Journal:

Pediatric Diabetes

Year:

2009

Language:

english

File:

PDF, 519 KB

english, 2009

5

The fetal insulin hypothesis: an alternative explanation of the association of low bir thweight with diabetes and vascular disease

Andrew T Hattersley, John E Tooke

Journal:

Year:

1999

Language:

english

File:

PDF, 100 KB

english, 1999

6

HNF1B-associated renal and extra-renal disease—an expanding clinical spectrum

Clissold, Rhian L., Hamilton, Alexander J., Hattersley, Andrew T., Ellard, Sian, Bingham, Coralie

Journal:

Nature Reviews Nephrology (formerly Nature Clinical Practice Nephrology)

Year:

2014

Language:

english

File:

PDF, 1.52 MB

english, 2014

7

Ethnic subgroup differences in hypertension in Pakistan

Jafar, Tazeen H, Levey, Andrew S, Jafary, Fahim H, White, Franklin, Gul, Asma, Rahbar, Mohammad H, Khan, Abdul Q, Hattersley, Andrew, Schmid, Christopher H, Chaturvedi, Nish

Journal:

Journal of Hypertension

Year:

2003

Language:

english

File:

PDF, 128 KB

english, 2003

8

A Type 1 Diabetes Genetic Risk Score Can Identify Patients With GAD65 Autoantibody–Positive Type 2 Diabetes Who Rapidly Progress to Insulin Therapy

Grubb, Anita L., McDonald, Timothy J., Rutters, Femke, Donnelly, Louise A., Hattersley, Andrew T., Oram, Richard A., Palmer, Colin N.A., van der Heijden, Amber A., Carr, Fiona, Elders, Petra J.M., Wee

Journal:

Year:

2018

Language:

english

File:

PDF, 714 KB

english, 2018

9

Disease progression and treatment response in data-driven subgroups of type 2 diabetes compared with models based on simple clinical features: an analysis using clinical trial data

Dennis, John M, Shields, Beverley M, Henley, William E, Jones, Angus G, Hattersley, Andrew T

Journal:

The Lancet Diabetes & Endocrinology

Year:

2019

Language:

english

File:

PDF, 480 KB

english, 2019

10

Identifying routine clinical predictors of non‐adherence to second‐line therapies in type 2 diabetes: A retrospective cohort analysis in a large primary care database

Shields, Beverley M., Hattersley, Andrew T., Farmer, Andrew J.

Journal:

Diabetes, Obesity and Metabolism

Year:

2019

Language:

english

File:

PDF, 944 KB

english, 2019

11

Type 2 Diabetes and COVID-19âRelated Mortality in the Critical Care Setting: A National Cohort Study in England, MarchâJuly 2020

Dennis, John M., Mateen, Bilal A., Sonabend, Raphael, Thomas, Nicholas J., Patel, Kashyap A., Hattersley, Andrew T., Denaxas, Spiros, McGovern, Andrew P., Vollmer, Sebastian J.

Journal:

Year:

2020

File:

PDF, 778 KB

2020

12

Loss of HNF1α function in human renal cell carcinoma: Frequent mutations in the VHL gene but not the HNF1α gene

Ira Lemm, Anja Lingott, Elke Pogge v. Strandmann, Christiane Zoidl, Michael P. Bulman, Andrew T. Hattersley, Wolfgang A. Schulz, Thomas Ebert, Gerhart U. Ryffel

Journal:

Molecular Carcinogenesis

Year:

1999

Language:

english

File:

PDF, 241 KB

english, 1999

13

Proposed mechanism for a novel insertion/deletion frameshift mutation (I414G415ATCG→CCA) in the hepatocyte nuclear factor 1 alpha (HNF-1α) gene which causes maturity-onset diabetes of the young (MODY)

Sian Ellard, Michael P. Bulman, Timothy M. Frayling, Maggie Shepherd, Andrew T. Hattersley

Journal:

Year:

2000

Language:

english

File:

PDF, 130 KB

english, 2000

14

A powerful approach to sub-phenotype analysis in population-based genetic association studies

Andrew P. Morris, Cecilia M. Lindgren, Eleftheria Zeggini, Nicholas J. Timpson, Timothy M. Frayling, Andrew T. Hattersley, Mark I. McCarthy

Journal:

Genetic Epidemiology

Year:

2010

Language:

english

File:

PDF, 298 KB

english, 2010

15

KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes

Ornella Massa, Dario Iafusco, Elena D'Amato, Anna L. Gloyn, Andrew T. Hattersley, Bruno Pasquino, Giorgio Tonini, Francesco Dammacco, Giorgio Zanette, Franco Meschi, Ottavia Porzio, Gianfranco Bottazz

Journal:

Year:

2005

Language:

english

File:

PDF, 169 KB

english, 2005

16

Heterometallic octahedral boride cluster chemistry :reactions of [Rh2Ru4 (CO) 16B] −with PPh3 P (OMe) 3 and the crystalstructures of [Rh2Ru4 (CO) 16B(AuPPh3) ] [Rh2Ru4 (CO) 14 (PPh3) 2B (AuPPh3) ]

Andrew D. Hattersley, Catherine E. Housecroft, Louise M. Liable-Sands, Arnold L. Rheingold, Anne Waller

Journal:

Year:

1998

Language:

english

File:

PDF, 658 KB

english, 1998

17

Variants in the aromatase gene and on the Y-chromosome are not associated with adult height or insulin resistance in a UK population

Michael N. Weedon, Martina Turner, Beatrice Knight, Penny Clark, Andrew T. Hattersley, Timothy M. Frayling

Journal:

Clinical Endocrinology

Year:

2003

Language:

english

File:

PDF, 83 KB

english, 2003

18

Response to treatment with rosiglitazone in familial partial lipodystrophy due to a mutation in the LMNA gene

Katharine R. Owen, Mollie Donohoe, Sian Ellard, Andrew T. Hattersley

Journal:

Diabetic Medicine

Year:

2003

Language:

english

File:

PDF, 97 KB

english, 2003

19

FTOgene variation and measures of body mass in an African population

Branwen J Hennig, Anthony J Fulford, Giorgio Sirugo, Pura Rayco-Solon, Andrew T Hattersley, Timothy M Frayling, Andrew M Prentice

Journal:

BMC Medical Genetics

Year:

2009

Language:

english

File:

PDF, 553 KB

english, 2009

20

The functional "KL-VS" variant ofKLOTHOis not associated with type 2 diabetes in 5028 UK Caucasians

Rachel M Freathy, Michael N Weedon, David Melzer, Beverley Shields, Graham A Hitman, Mark Walker, Mark I McCarthy, Andrew T Hattersley, Timothy M Frayling

Journal:

BMC Medical Genetics

Year:

2006

Language:

english

File:

PDF, 502 KB

english, 2006

21

A study of association between common variation in the growth hormone-chorionic somatomammotropin hormone gene cluster and adult fasting insulin in a UK Caucasian population

Rachel M Freathy, Simon MS Mitchell, Beatrice Knight, Beverley Shields, Michael N Weedon, Andrew T Hattersley, Timothy M Frayling

Journal:

Journal of Negative Results in BioMedicine

Year:

2006

Language:

english

File:

PDF, 518 KB

english, 2006

22

Syntheses and structural characterizations of the octahedral boride clusters [Rh2Ru4H(CO)16−2x(nbd)xB] (x=1,2) and gold(I) phosphine derivatives (nbd=norbornadiene)

Andrew D. Hattersley, Catherine E. Housecroft, Arnold L. Rheingold

Journal:

Journal of Cluster Science

Year:

1997

Language:

english

File:

PDF, 750 KB

english, 1997

23

Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes

Janniche Torsvik, Stefan Johansson, Anders Johansen, Jakob Ek, Jayne Minton, Helge Ræder, Sian Ellard, Andrew Hattersley, Oluf Pedersen, Torben Hansen, Anders Molven, Pål R. Njølstad

Journal:

Year:

2010

Language:

english

File:

PDF, 309 KB

english, 2010

24

The versatile nature of [ClAu(L–L)AuCl] (L–L=bis(diphenylphosphino)methane (dppm) or -butane (dppb)) in reactions with [Rh2Ru4(CO)16B]−: crystal structures of [{Rh2Ru4(CO)16B}2{μ-Au(dppb)Au}] and [RhRu4(CO)14B{Au(dppm)Au}]

Andrew D Hattersley, Catherine E Housecroft, Arnold L Rheingold

Journal:

Inorganica Chimica Acta

Year:

1999

Language:

english

File:

PDF, 244 KB

english, 1999

25

Boride cluster fusion through copper and silver. Crystal structure of [(Ph3P)2N][(HRu4(CO)12BH)2Ag]

Catherine E Housecroft, Sylvia M Draper, Andrew D Hattersley, Arnold L Rheingold

Journal:

Journal of Organometallic Chemistry

Year:

2000

Language:

english

File:

PDF, 152 KB

english, 2000

26

Tall stories: the fundamental difficulties of genetic association studies

Michael N. Weedon, Andrew T. Hattersley, Timothy M. Frayling

Journal:

Clinical Endocrinology

Year:

2004

Language:

english

File:

PDF, 168 KB

english, 2004

27

Premature birth and low birth weight associated with nonautoimmune hyperthyroidism due to an activating thyrotropin receptor gene mutation

Bijay Vaidya, Viv Campbell, John H. Tripp, Gill Spyer, Andrew T. Hattersley, Sian Ellard

Journal:

Clinical Endocrinology

Year:

2004

Language:

english

File:

PDF, 133 KB

english, 2004

28

Mutations in the ABCC8 (SUR1 subunit of the KATP channel) gene are associated with a variable clinical phenotype

Tomasz Klupa, Irina Kowalska, Krystyna Wyka, Jan Skupien, Ann-Marie Patch, Sarah E. Flanagan, Anna Noczynska, Malgorzata Arciszewska, Sian Ellard, Andrew T. Hattersley, Jacek Sieradzki, Wojciech Mlyna

Journal:

Clinical Endocrinology

Year:

2009

Language:

english

File:

PDF, 105 KB

english, 2009

29

The accuracy of birth weight

Elizabeth Stenhouse, David E Wright, Andrew T Hattersley, Ann Millward

Journal:

Journal of Clinical Nursing

Year:

2004

Language:

english

File:

PDF, 47 KB

english, 2004

30

The Exeter Family Study of Childhood Health (EFSOCH): study protocol and methodology

Bridget Knight, Beverley M. Shields, Andrew T. Hattersley

Journal:

Paediatric and Perinatal Epidemiology

Year:

2006

Language:

english

File:

PDF, 110 KB

english, 2006

31

ISPAD Clinical Practice Consensus Guidelines 2006–2007 Definition, epidemiology and classification

Maria E Craig, Andrew Hattersley, Kim Donaghue

Journal:

Pediatric Diabetes

Year:

2006

Language:

english

File:

PDF, 129 KB

english, 2006

32

ISPAD Clinical Practice Consensus Guidelines 2006–2007 The diagnosis and management of monogenic diabetes in children

Andrew Hattersley, Jan Bruining, Julian Shield, Pal Njolstad, Kim Donaghue

Journal:

Pediatric Diabetes

Year:

2006

Language:

english

File:

PDF, 113 KB

english, 2006

33

Genetics and type 2 diabetes in youth

Olivia Gill-Carey, Andrew T Hattersley

Journal:

Pediatric Diabetes

Year:

2007

Language:

english

File:

PDF, 86 KB

english, 2007

34

Incidence of neonatal diabetes in Austria–calculation based on the Austrian Diabetes Register

Barbara Wiedemann, Edith Schober, Thomas Waldhoer, Julia Koehle, Sarah E Flanagan, Deborah JG Mackay, Elisabeth Steichen, Dagmar Meraner, Lothar-Bernd Zimmerhackl, Andrew T Hattersley, Sian Ellard, Sa

Journal:

Pediatric Diabetes

Year:

2010

Language:

english

File:

PDF, 490 KB

english, 2010

35

Definition, epidemiology and classification of diabetes in children and adolescents

Maria E. Craig, Andrew Hattersley, Kim C. Donaghue

Journal:

Pediatric Diabetes

Year:

2009

Language:

english

File:

PDF, 532 KB

english, 2009

36

Persistently autoantibody negative (PAN) type 1 diabetes mellitus in children

Shihab Hameed, Sian Ellard, Helen J Woodhead, Kristen A Neville, Jan L Walker, Maria E Craig, Taylor Armstrong, Liping Yu, George S Eisenbarth, Andrew T Hattersley, Charles F Verge

Journal:

Pediatric Diabetes

Year:

2011

Language:

english

File:

PDF, 519 KB

english, 2011

37

KCNJ11 activating mutations cause both transient and permanent neonatal diabetes mellitus in Cypriot patients

Yiannis S. Ioannou, Sian Ellard, Andrew Hattersley, Nicos Skordis

Journal:

Pediatric Diabetes

Year:

2011

Language:

english

File:

PDF, 495 KB

english, 2011

38

Genome-Wide Association Scan Allowing for Epistasis in Type 2 Diabetes

Jordana T. Bell, Nicholas J. Timpson, N. William Rayner, Eleftheria Zeggini, Timothy M. Frayling, Andrew T. Hattersley, Andrew P. Morris, Mark I. McCarthy

Journal:

Annals of Human Genetics

Year:

2011

Language:

english

File:

PDF, 276 KB

english, 2011

39

Neonatal hyperinsulinaemic hypoglycaemia and monogenic diabetes due to a heterozygous mutation of the HNF4A gene

Jennifer J. CONN, Peter J. SIMM, Jeremy J. N. OATS, Alison J. NANKERVIS, Susan E. JACOBS, Sian ELLARD, Andrew T. HATTERSLEY

Journal:

Australian and New Zealand Journal of Obstetrics and Gynaecology

Year:

2009

Language:

english

File:

PDF, 976 KB

english, 2009

40

10.1038/74321

Turnpenny, Peter D., Bulman, Michael P., Kusumi, Kenro, Frayling, Timothy M., McKeown, Carole, Garrett, Christine, Lander, Eric S., Krumlauf, Robb, Hattersley, Andrew T., Ellard, Sian

Journal:

Nature Biotechnology

Year:

2000

Language:

english

File:

PDF, 95 KB

english, 2000

41

10.1038/74307

Turnpenny, Peter D., Bulman, Michael P., Kusumi, Kenro, Frayling, Timothy M., McKeown, Carole, Garrett, Christine, Lander, Eric S., Krumlauf, Robb, Hattersley, Andrew T., Ellard, Sian

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 883 KB

english, 2000

42

10.1038/953

Hattersley, Andrew T., Beards, Frances, Ballantyne, Elizabeth, Appleton, Maggie, Harvey, Rod, Ellard, Sian

Journal:

Nature Genetics

Year:

1998

Language:

english

File:

PDF, 51 KB

english, 1998

43

A mutation (R826W) in nucleotide-binding domain 1 of ABCC8 reduces ATPase activity and causes transient neonatal diabetes

de Wet, Heidi, Proks, Peter, Lafond, Mathilde, Aittoniemi, Jussi, Sansom, Mark S P, Flanagan, Sarah E, Pearson, Ewan R, Hattersley, Andrew T, Ashcroft, Frances M

Journal:

Year:

2008

Language:

english

File:

PDF, 349 KB

english, 2008

44

Beyond the beta cell in diabetes

Hattersley, Andrew T

Journal:

Nature Genetics

Year:

2006

Language:

english

File:

PDF, 132 KB

english, 2006

45

Mutations in PTF1A cause pancreatic and cerebellar agenesis

Sellick, Gabrielle S, Barker, Karen T, Stolte-Dijkstra, Irene, Fleischmann, Christina, J Coleman, Richard, Garrett, Christine, Gloyn, Anna L, Edghill, Emma L, Hattersley, Andrew T, Wellauer, Peter K

Journal:

Nature Genetics

Year:

2004

Language:

english

File:

PDF, 582 KB

english, 2004

46

An evaluation of HapMap sample size and tagging SNP performance in large-scale empirical and simulated data sets

Zeggini, Eleftheria, Rayner, William, Morris, Andrew P, Hattersley, Andrew T, Walker, Mark, Hitman, Graham A, Deloukas, Panos, Cardon, Lon R, McCarthy, Mark I

Journal:

Nature Genetics

Year:

2005

Language:

english

File:

PDF, 118 KB

english, 2005

47

KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological features

Gloyn, Anna L, Diatloff-Zito, Catherine, Edghill, Emma L, Bellanné-Chantelot, Christine, Nivot, Sylvie, Coutant, Régis, Ellard, Sian, Hattersley, Andrew T, Robert, Jean Jacques

Journal:

European Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 131 KB

english, 2006

48

A gating mutation at the internal mouth of the Kir6.2 pore is associated with DEND syndrome

Proks, Peter, Girard, Christophe, Haider, Shozeb, Gloyn, Anna L, Hattersley, Andrew T, Sansom, Mark S P, Ashcroft, Frances M

Journal:

Year:

2005

Language:

english

File:

PDF, 273 KB

english, 2005

49

A conserved tryptophan at the membrane–water interface acts as a gatekeeper for Kir6.2/SUR1 channels and causes neonatal diabetes when mutated

Roope Männikkö, Phillip J. Stansfeld, Alexandra S. Ashcroft, Andrew T. Hattersley, Mark S. P. Sansom, Sian Ellard, Frances M. Ashcroft

Journal:

The Journal of Physiology

Year:

2011

Language:

english

File:

PDF, 795 KB

english, 2011

50

Mutations in the hepatocyte nuclear factor-1β (HNF1B) gene are common with combined uterine and renal malformations but are not found with isolated uterine malformations

Richard A. Oram, Emma L. Edghill, Jenny Blackman, Miles J.O. Taylor, Tracey Kay, Sarah E. Flanagan, Ida Ismail-Pratt, Sarah M. Creighton, Sian Ellard, Andrew T. Hattersley, Coralie Bingham

Journal:

American Journal of Obstetrics and Gynecology

Year:

2010

Language:

english

File:

PDF, 215 KB

english, 2010