1-9 of 9
Mark Lathrop
Close
Save search
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Journal Articles

Impact of Common Variation in Bone-Related Genes on Type 2 Diabetes and Related Traits

Open Access
Liana K. Billings, Yi-Hsiang Hsu, Rachel J. Ackerman, Josée Dupuis, Benjamin F. Voight, Laura J. Rasmussen-Torvik, Serge Hercberg, Mark Lathrop, Daniel Barnes, Claudia Langenberg, Jennie Hui, Mao Fu, Nabila Bouatia-Naji, Cecile Lecoeur, Ping An, Patrik K. Magnusson, Ida Surakka, Samuli Ripatti, Lene Christiansen, Christine Dalgård, Lasse Folkersen, Elin Grundberg, the MAGIC Investigators, the DIAGRAM + Consortium, the MuTHER Consortium, the ASCOT Investigators, the GEFOS Consortium, Per Eriksson, Jaakko Kaprio, Kirsten Ohm Kyvik, Nancy L. Pedersen, Ingrid B. Borecki, Michael A. Province, Beverley Balkau, Philippe Froguel, Alan R. Shuldiner, Lyle J. Palmer, Nick Wareham, Pierre Meneton, Toby Johnson, James S. Pankow, David Karasik, James B. Meigs, Douglas P. Kiel, Jose C. Florez
Journal: Diabetes
Diabetes 2012;61(8):2176–2186
https://doi.org/10.2337/db11-1515
Published: 17 July 2012
View article titled, Impact of Common Variation in Bone-Related Genes on Type 2 Diabetes and Related Traits
Open the PDF for Impact of Common Variation in Bone-Related Genes on Type 2 Diabetes and Related Traits in another window
Includes: Supplementary data
Journal Articles

G/T Substitution in Intron 1 of the UNC13B Gene Is Associated With Increased Risk of Nephropathy in Patients With Type 1 Diabetes

Free
David-Alexandre Trégouet, Per-Henrik Groop, Steven McGinn, Carol Forsblom, Samy Hadjadj, Michel Marre, Hans-Henrik Parving, Lise Tarnow, Ralph Telgmann, Tiphaine Godefroy, Viviane Nicaud, Rachel Rousseau, Maikki Parkkonen, Anna Hoverfält, Ivo Gut, Simon Heath, Fumihiko Matsuda, Roger Cox, Gbenga Kazeem, Martin Farrall, Dominique Gauguier, Stefan-Martin Brand-Herrmann, François Cambien, Mark Lathrop, Nathalie Vionnet, for the EURAGEDIC Consortium
Journal: Diabetes
Diabetes 2008;57(10):2843–2850
https://doi.org/10.2337/db08-0073
Published: 01 October 2008
View article titled, G/T Substitution in Intron 1 of the UNC13B Gene Is Associated With Increased Risk of Nephropathy in Patients With Type 1 Diabetes
Open the PDF for G/T Substitution in Intron 1 of the UNC13B Gene Is Associated With Increased Risk of Nephropathy in Patients With Type 1 Diabetes in another window
Includes: Supplementary data
Journal Articles

Association Analysis Indicates That a Variant GATA-Binding Site in the PIK3CB Promoter Is a Cis-Acting Expression Quantitative Trait Locus for This Gene and Attenuates Insulin Resistance in Obese Children

Free
Catherine Le Stunff, Agnès Dechartres, Virginie Mariot, Chantal Lotton, Cecelia Trainor, Emanuele Miraglia Del Giudice, David Meyre, Ivan Bieche, Ingrid Laurendeau, Philippe Froguel, Diana Zelenika, Dani Fallin, Mark Lathrop, Paul-Henri Roméo, Pierre Bougnères
Journal: Diabetes
Diabetes 2008;57(2):494–502
https://doi.org/10.2337/db07-1273
Published: 01 February 2008
View article titled, Association Analysis Indicates That a Variant GATA-Binding Site in the PIK3CB Promoter Is a Cis-Acting Expression Quantitative Trait Locus for This Gene and Attenuates Insulin Resistance in Obese Children
Open the PDF for Association Analysis Indicates That a Variant GATA-Binding Site in the PIK3CB Promoter Is a Cis-Acting Expression Quantitative Trait Locus for This Gene and Attenuates Insulin Resistance in Obese Children in another window
Journal Articles

Quantitative Trait Loci for Fasting Glucose in Young Europeans Replicate Previous Findings for Type 2 Diabetes in 2q23–24 and Other Locations

Free
Delphine Fradin, Simon Heath, Mark Lathrop, Pierre Bougnères
Journal: Diabetes
Diabetes 2007;56(6):1742–1745
https://doi.org/10.2337/db06-1329
Published: 01 June 2007
View article titled, Quantitative Trait Loci for Fasting Glucose in Young Europeans Replicate Previous Findings for Type 2 Diabetes in 2q23–24 and Other Locations
Open the PDF for Quantitative Trait Loci for Fasting Glucose in Young Europeans Replicate Previous Findings for Type 2 Diabetes in 2q23–24 and Other Locations in another window
Journal Articles

Analysis of 14 Candidate Genes for Diabetic Nephropathy on Chromosome 3q in European Populations : Strongest Evidence for Association With a Variant in the Promoter Region of the Adiponectin Gene

Free
Nathalie Vionnet, David Tregouët, Gbenga Kazeem, Ivo Gut, Per-Henrik Groop, Lise Tarnow, Hans-Henrik Parving, Samy Hadjadj, Carol Forsblom, Martin Farrall, Dominique Gauguier, Roger Cox, Fumihiko Matsuda, Simon Heath, Alexandre Thévard, Rachel Rousseau, François Cambien, Michel Marre, Mark Lathrop
Journal: Diabetes
Diabetes 2006;55(11):3166–3174
https://doi.org/10.2337/db06-0271
Published: 01 November 2006
View article titled, Analysis of 14 Candidate Genes for Diabetic Nephropathy on Chromosome 3q in European Populations : Strongest Evidence for Association With a Variant in the Promoter Region of the Adiponectin Gene
Open the PDF for Analysis of 14 Candidate Genes for Diabetic Nephropathy on Chromosome 3q in European Populations : Strongest Evidence for Association With a Variant in the Promoter Region of the Adiponectin Gene in another window
Includes: Supplementary data
Journal Articles

Wolcott-Rallison Syndrome: Clinical, Genetic, and Functional Study of EIF2AK3 Mutations and Suggestion of Genetic Heterogeneity

Free
Valérie Senée, Krishna M. Vattem, Marc Delépine, Lynn A. Rainbow, Céline Haton, Annick Lecoq, Nick J. Shaw, Jean-Jacques Robert, Raoul Rooman, Catherine Diatloff-Zito, Jacques L. Michaud, Bassan Bin-Abbas, Doris Taha, Bernard Zabel, Piergiorgio Franceschini, A. Kemal Topaloglu, G. Mark Lathrop, Timothy G. Barrett, Marc Nicolino, Ronald C. Wek, Cécile Julier
Journal: Diabetes
Diabetes 2004;53(7):1876–1883
https://doi.org/10.2337/diabetes.53.7.1876
Published: 01 July 2004
View article titled, Wolcott-Rallison Syndrome: Clinical, Genetic, and Functional Study of EIF2AK3 Mutations and Suggestion of Genetic Heterogeneity
Open the PDF for Wolcott-Rallison Syndrome: Clinical, Genetic, and Functional Study of EIF2AK3 Mutations and Suggestion of Genetic Heterogeneity in another window
Journal Articles

Polymorphisms in Type II SH2 Domain–Containing Inositol 5-Phosphatase (INPPL1, SHIP2) Are Associated With Physiological Abnormalities of the Metabolic Syndrome

Free
Pamela J. Kaisaki, Marc Delépine, Peng Y. Woon, Liam Sebag-Montefiore, Steven P. Wilder, Stephan Menzel, Nathalie Vionnet, Evelyne Marion, Jean-Pierre Riveline, Guillaume Charpentier, Stéphane Schurmans, Jonathan C. Levy, Mark Lathrop, Martin Farrall, Dominique Gauguier
Journal: Diabetes
Diabetes 2004;53(7):1900–1904
https://doi.org/10.2337/diabetes.53.7.1900
Published: 01 July 2004
View article titled, Polymorphisms in Type II SH2 Domain–Containing Inositol 5-Phosphatase (INPPL1, SHIP2) Are Associated With Physiological Abnormalities of the Metabolic Syndrome
Open the PDF for Polymorphisms in Type II SH2 Domain–Containing Inositol 5-Phosphatase (INPPL1, SHIP2) Are Associated With Physiological Abnormalities of the Metabolic Syndrome in another window
Includes: Supplementary data
Journal Articles

Prevalence of Mutations in AGPAT2 Among Human Lipodystrophies

Free
Jocelyne Magré, Marc Delépine, Lionel Van Maldergem, Jean-Jacques Robert, J. Antonie Maassen, Muriel Meier, Vanessa R. Panz, Chong Ae Kim, Nadia Tubiana-Rufi, Paul Czernichow, Eva Seemanova, Charles R. Buchanan, Didier Lacombe, Corinne Vigouroux, Olivier Lascols, C. Ronald Kahn, Jacqueline Capeau, Mark Lathrop
Journal: Diabetes
Diabetes 2003;52(6):1573–1578
https://doi.org/10.2337/diabetes.52.6.1573
Published: 01 June 2003
View article titled, Prevalence of Mutations in AGPAT2 Among Human Lipodystrophies
Open the PDF for Prevalence of Mutations in AGPAT2 Among Human Lipodystrophies in another window
Journal Articles

Molecular Analysis of Berardinelli-Seip Congenital Lipodystrophy in Oman: Evidence for Multiple Loci

Free
Kirsten Heathcote, Anna Rajab, Jocelyne Magré, Petros Syrris, Mehran Besti, Michael Patton, Marc Délépine, Mark Lathrop, Jacqueline Capeau, Steve Jeffery
Journal: Diabetes
Diabetes 2002;51(4):1291–1293
https://doi.org/10.2337/diabetes.51.4.1291
Published: 01 April 2002
View article titled, Molecular Analysis of Berardinelli-Seip Congenital Lipodystrophy in Oman: Evidence for Multiple Loci
Open the PDF for Molecular Analysis of Berardinelli-Seip Congenital Lipodystrophy in Oman: Evidence for Multiple Loci in another window