CrossRef Cited By Search Results

This article [doi:10.1038/ng1708] has been cited in the following papers, taken from those publishers and societies that are participating in CrossRef's Cited-by Linking service. The number of citations from this service is usually lower than citation numbers from databases that include more journals.

1. EISSN: 17448352 ISSN: 14737159

   Expert Review of Molecular Diagnostics

   Genetic contributions to Type�2 diabetes: recent insights

   Michèle M Sale, Stephen S Rich

   7 (2), 2007, p.207

   doi:10.1586/14737159.7.2.207

2. EISSN: 17447666 ISSN: 14656566

   Expert Opinion on Pharmacotherapy

   Defining the genetic aetiology of monogenic diabetes can improve treatment

   Anna L Gloyn, Sian Ellard

   7 (13), 2006, p.1759

   doi:10.1517/14656566.7.13.1759

3. EISSN: 13990004 ISSN: 00099163

   Clinical Genetics

   Identification of novel and recurrent glucokinase mutations in Belgian and Luxembourg maturity onset diabetes of the young patients

   L Vits et al.

   70 (4), 2006, p.355

   doi:10.1111/j.1399-0004.2006.00686.x

4. EISSN: 14764687 ISSN: 00280836

   Nature

   Human genetics illuminates the paths to metabolic disease

   Stephen O’Rahilly

   462 (7271), 2009, p.307

   doi:10.1038/nature08532

5. EISSN: 15461718 ISSN: 10614036

   Nature Genetics

   Beyond the beta cell in diabetes

   Andrew T Hattersley

   38 (1), 2006, p.12

   doi:10.1038/ng0106-12

6. EISSN: 10916490 ISSN: 00278424

   Proceedings of the National Academy of Sciences

   Mutations at the BLK locus linked to maturity onset diabetes of the young and  -cell dysfunction

   M. Borowiec et al.

   106 (34), 2009, p.14460

   doi:10.1073/pnas.0906474106

7. EISSN: 13995448 ISSN: 1399543X

   Pediatric Diabetes

   The diagnosis and management of monogenic diabetes in children and adolescents

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

   p.33

   doi:10.1111/j.1399-5448.2009.00571.x

8. EISSN: 14321203 ISSN: 03406717

   Human Genetics

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

   Janniche Torsvik et al.

   doi:10.1007/s00439-009-0740-8

9. EISSN: 14320428 ISSN: 0012186X

   Diabetologia

   Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the young

   S. Ellard, C. Bellanné-Chantelot, A. T. Hattersley

   51 (4), 2008, p.546

   doi:10.1007/s00125-008-0942-y

10. EISSN: 13995448 ISSN: 1399543X

    Pediatric Diabetes

    Differential diagnosis of type 1 diabetes: which genetic syndromes need to be considered?

    Timothy Geoffrey Barrett

    8 (s6), 2007, p.15

    doi:10.1111/j.1399-5448.2007.00278.x

11. EISSN: 1744828X ISSN: 17410541

    Personalized Medicine

    Monogenic disorders of the pancreatic ?-cell: personalizing treatment for rare forms of diabetes and hypoglycemia

    Martijn van de Bunt, Anna L Gloyn

    4 (3), 2007, p.247

    doi:10.2217/17410541.4.3.247

12. EISSN: 13995448 ISSN: 1399543X

    Pediatric Diabetes

    Childhood obesity complicating the differential diagnosis of maturity-onset diabetes of the young and type 2 diabetes

    Naomi Weintrob, Eti Stern, Yaffa Klipper-Aurbach, Moshe Phillip, Galia Gat-Yablonski

    0 (0), 2007, p.071127170524002

    doi:10.1111/j.1399-5448.2007.00259.x

13. EISSN: 13995448 ISSN: 1399543X

    Pediatric Diabetes

    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

    7 (6), 2006, p.352

    doi:10.1111/j.1399-5448.2006.00217.x

14. EISSN: 15461718 ISSN: 10614036

    Nature Genetics

    Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism

    Valérie Senée et al.

    38 (6), 2006, p.682

    doi:10.1038/ng1802

15. EISSN: 13652265 ISSN: 03000664

    Clinical Endocrinology

    Haploinsufficiency at GCK gene is not a frequent event in MODY2 patients

    Intza Garin et al.

    68 (6), 2008, p.873

    doi:10.1111/j.1365-2265.2008.03214.x

16. EISSN: 17458374 ISSN: 17458366

    Nature Clinical Practice Endocrinology & Metabolism

    Clinical implications of a molecular genetic classification of monogenic β-cell diabetes

    Rinki Murphy, Sian Ellard, Andrew T Hattersley

    4 (4), 2008, p.200

    doi:10.1038/ncpendmet0778

17. EISSN: 16443640 ISSN: 18951058

    Central European Journal of Medicine

    Successful discontinuation of insulin treatment after gestational diabetes is shown to be a case of MODY due to a glucokinase mutation

    Indrajit Talapatra, Shyam Kalavalapalli, Jonathan Mark Robinson, Sian Ellard, David James Tymms

    3 (2), 2008, p.225

    doi:10.2478/s11536-007-0065-8

18. EISSN: 14645491 ISSN: 07423071

    Diabetic Medicine

    Prevalence of HNF1A (MODY3) mutations in a Norwegian population (the HUNT2 Study)

    S. . Eide et al.

    25 (7), 2008, p.775

    doi:10.1111/j.1464-5491.2008.02459.x

19. EISSN: 14645491 ISSN: 07423071

    Diabetic Medicine

    Pancreatic exocrine insufficiency is not common in HNF-1α MODY

    T. Klupa et al.

    25 (5), 2008, p.627

    doi:10.1111/j.1464-5491.2008.02432.x

20. EISSN: 17448417 ISSN: 17446651

    Expert Review of Endocrinology & Metabolism

    Function of HNF1 in the pathogenesis of diabetes

    David B Rhoads, Lynne L Levitsky

    3 (3), 2008, p.391

    doi:10.1586/17446651.3.3.391

21. EISSN: 14645491 ISSN: 07423071

    Diabetic Medicine

    Lack of pancreatic body and tail in HNF1B mutation carriers

    I. S. Haldorsen et al.

    25 (7), 2008, p.782

    doi:10.1111/j.1464-5491.2008.02460.x

22. EISSN: 13995448 ISSN: 1399543X

    Pediatric Diabetes

    Diagnostic screening of MODY2/GCK mutations in the Norwegian MODY Registry

    Jørn V Sagen et al.

    9 (5), 2008, p.442

    doi:10.1111/j.1399-5448.2008.00399.x

23. EISSN: 13995448 ISSN: 1399543X

    Pediatric Diabetes

    Growth factor control of pancreatic islet regeneration and function

    Anke Assmann, Charlotte Hinault, Rohit N Kulkarni

    10 (1), 2009, p.14

    doi:10.1111/j.1399-5448.2008.00468.x

24. EISSN: 13995448 ISSN: 1399543X

    Pediatric Diabetes

    Diabetes mellitus, exocrine pancreatic deficiency, hypertrichosis, hyperpigmentation, and chronic inflammation: confirmation of a syndrome

    Khalid Hussain et al.

    10 (3), 2009, p.193

    doi:10.1111/j.1399-5448.2008.00470.x