Works by Mohlke, Karen L.

Results: 70

A common frameshift mutation in von Willebrand factor does not alter mRNA stability but interferes with normal propeptide processing.
Published in:
British Journal of Haematology, 1996, v. 95, n. 1, p. 184, doi. 10.1046/j.1365-2141.1996.7572377.x
By:
- Mohlke, Karen L.;
- Nichols, William C.;
- Rehemtulla, Alnawaz;
- Kaufman, Randal J.;
- Fagerström, Heidi M.;
- Ritvanen, K. L. Annukka;
- Kekomäki, Riitta;
- Ginsburg, David
Publication type:
Article
Mitochondrial polymorphisms and susceptibility to type 2 diabetes-related traits in Finns.
Published in:
Human Genetics, 2005, v. 118, n. 2, p. 245, doi. 10.1007/s00439-005-0046-4
By:
- Mohlke, Karen L.;
- Jackson, Anne U.;
- Scott, Laura J.;
- Peck, Erin C.;
- Suh, Yong D.;
- Chines, Peter S.;
- Watanabe, Richard M.;
- Buchanan, Thomas A.;
- Conneely, Karen N.;
- Erdos, Michael R.;
- Narisu, Narisu;
- Enloe, Sareena;
- Valle, Timo T.;
- Tuomilehto, Jaakko;
- Bergman, Richard N.;
- Boehnke, Michael;
- Collins, Francis S.
Publication type:
Article
Open Chromatin Profiling in Adipose Tissue Marks Genomic Regions with Functional Roles in Cardiometabolic Traits.
Published in:
G3: Genes | Genomes | Genetics, 2019, v. 9, n. 8, p. 2521, doi. 10.1534/g3.119.400294
By:
- Cannon, Maren E.;
- Currin, Kevin W.;
- Young, Kristin L.;
- Perrin, Hannah J.;
- Vadlamudi, Swarooparani;
- Safi, Alexias;
- Lingyun Song;
- Ying Wu;
- Wabitsch, Martin;
- Laakso, Markku;
- Crawford, Gregory E.;
- Mohlke, Karen L.
Publication type:
Article
Trans-ancestry Fine Mapping and Molecular Assays Identify Regulatory Variants at the ANGPTL8 HDL-C GWAS Locus.
Published in:
G3: Genes | Genomes | Genetics, 2017, v. 7, n. 9, p. 3217, doi. 10.1534/g3.117.300088
By:
- Cannon, Maren E.;
- Qing Duan;
- Ying Wu;
- Zeynalzadeh, Monica;
- Zheng Xu;
- Kangas, Antti J.;
- Soininen, Pasi;
- Ala-Korpela, Mika;
- Civelek, Mete;
- Lusis, Aldons J.;
- Kuusisto, Johanna;
- Collins, Francis S.;
- Boehnke, Michael;
- Hua Tang;
- Laakso, Markku;
- Yun Li;
- Mohlke, Karen L.
Publication type:
Article
Integration of DNA sequencing with population pharmacokinetics to improve the prediction of irinotecan exposure in cancer patients.
Published in:
2022
By:
- Karas, Spinel;
- Etheridge, Amy S.;
- Nickerson, Deborah A.;
- Cox, Nancy J.;
- Mohlke, Karen L.;
- Cecchin, Erika;
- Toffoli, Giuseppe;
- Mathijssen, Ron H. J.;
- Forrest, Alan;
- Bies, Robert R.;
- Innocenti, Federico
Publication type:
journal article
Multi-SNP mediation intersection-union test.
Published in:
Bioinformatics, 2019, v. 35, n. 22, p. 4724, doi. 10.1093/bioinformatics/btz285
By:
- Zhong, Wujuan;
- Spracklen, Cassandra N;
- Mohlke, Karen L;
- Zheng, Xiaojing;
- Fine, Jason;
- Li, Yun
Publication type:
Article
HUGIn: Hi-C Unifying Genomic Interrogator.
Published in:
Bioinformatics, 2017, v. 33, n. 23, p. 3793, doi. 10.1093/bioinformatics/btx359
By:
- Martin, Joshua S.;
- Zheng Xu;
- Reiner, Alex P.;
- Mohlke, Karen L.;
- Sullivan, Patrick;
- Bing Ren;
- Ming Hu;
- Yun Li
Publication type:
Article
3D chromatin structure in chondrocytes identifies putative osteoarthritis risk genes.
Published in:
Genetics, 2022, v. 222, n. 4, p. 1, doi. 10.1093/genetics/iyac141
By:
- Thulson, Eliza;
- Davis, Eric S.;
- D’Costa, Susan;
- Coryell, Philip R.;
- Kramer, Nicole E.;
- Mohlke, Karen L.;
- Loeser, Richard F.;
- Diekman, Brian O.;
- Phanstiel, Douglas H.
Publication type:
Article
Single-nucleotide polymorphisms at five loci are associated with C-reactive protein levels in a cohort of Filipino young adults.
Published in:
Journal of Human Genetics, 2011, v. 56, n. 12, p. 823, doi. 10.1038/jhg.2011.106
By:
- Curocichin, Ghenadie;
- Wu, Ying;
- McDade, Thomas W;
- Kuzawa, Christopher W;
- Borja, Judith B;
- Qin, Li;
- Lange, Ethan M;
- Adair, Linda S;
- Lange, Leslie A;
- Mohlke, Karen L
Publication type:
Article
Comparison of ENCODE region SNPs between Cebu Filipino and Asian HapMap samples.
Published in:
Journal of Human Genetics, 2007, v. 52, n. 9, p. 729, doi. 10.1007/s10038-007-0175-9
By:
- Marvelle, Amanda F.;
- Lange, Leslie A.;
- Li Qin;
- Yunfei Wang;
- Lange, Ethan M.;
- Adair, Linda S.;
- Mohlke, Karen L.
Publication type:
Article
Population-specific coding variant underlies genome-wide association with adiponectin level.
Published in:
Human Molecular Genetics, 2012, v. 21, n. 2, p. 463, doi. 10.1093/hmg/ddr480
By:
- Croteau-Chonka, Damien C.;
- Wu, Ying;
- Li, Yun;
- Fogarty, Marie P.;
- Lange, Leslie A.;
- Kuzawa, Christopher W.;
- McDade, Thomas W.;
- Borja, Judith B.;
- Luo, Jingchun;
- AbdelBaky, Omar;
- Combs, Terry P.;
- Adair, Linda S.;
- Lange, Ethan M.;
- Mohlke, Karen L.
Publication type:
Article
Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1–ADIPOQ.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 24, p. 4955, doi. 10.1093/hmg/ddq423
By:
- Wu, Ying;
- Li, Yun;
- Lange, Ethan M.;
- Croteau-Chonka, Damien C.;
- Kuzawa, Christopher W.;
- McDade, Thomas W.;
- Qin, Li;
- Curocichin, Ghenadie;
- Borja, Judith B.;
- Lange, Leslie A.;
- Adair, Linda S.;
- Mohlke, Karen L.
Publication type:
Article
Allelic expression imbalance at high-density lipoprotein cholesterol locus MMAB-MVK.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 10, p. 1921, doi. 10.1093/hmg/ddq067
By:
- Fogarty, Marie P.;
- Xiao, Rui;
- Prokunina-Olsson, Ludmila;
- Scott, Laura J.;
- Mohlke, Karen L.
Publication type:
Article
Genome-wide association study of homocysteine levels in Filipinos provides evidence for CPS1 in women and a stronger MTHFR effect in young adults.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 10, p. 2050, doi. 10.1093/hmg/ddq062
By:
- Lange, Leslie A.;
- Croteau-Chonka, Damien C.;
- Marvelle, Amanda F.;
- Qin, Li;
- Gaulton, Kyle J.;
- Kuzawa, Christopher W.;
- McDade, Thomas W.;
- Wang, Yunfei;
- Li, Yun;
- Levy, Shawn;
- Borja, Judith B.;
- Lange, Ethan M.;
- Adair, Linda S.;
- Mohlke, Karen L.
Publication type:
Article
Metabolic and cardiovascular traits: an abundance of recently identified common genetic variants.
Published in:
Human Molecular Genetics, 2008, v. 17, n. R2, p. R102, doi. 10.1093/hmg/ddn275
By:
- Mohlke, Karen L.;
- Boehnke, Michael;
- Abecasis, Gonçalo R.
Publication type:
Article
Identification of Novel Candidate Genes and Variants for Hearing Loss and Temporal Bone Anomalies.
Published in:
Genes, 2021, v. 12, n. 4, p. 566, doi. 10.3390/genes12040566
By:
- Santos-Cortez, Regie Lyn P.;
- Yarza, Talitha Karisse L.;
- Bootpetch, Tori C.;
- Tantoco, Ma. Leah C.;
- Mohlke, Karen L.;
- Cruz, Teresa Luisa G.;
- Chiong Perez, Mary Ellen;
- Chan, Abner L.;
- Lee, Nanette R.;
- Tobias-Grasso, Celina Ann M.;
- Reyes-Quintos, Maria Rina T.;
- Cutiongco-de la Paz, Eva Maria;
- Chiong, Charlotte M.
Publication type:
Article
Association of FTO With Obesity-Related Traits in the Cebu Longitudinal Health and Nutrition Survey (CLHNS) Cohort.
Published in:
Diabetes, 2008, v. 57, n. 7, p. 1987, doi. 10.2337/db07-1700
By:
- Marvelle, Amanda F.;
- Lange, Leslie A.;
- Qin, Li;
- Mohlke, Karen L.;
- Adair, Linda S.
Publication type:
Article
Association of Transcription Factor 7-Like 2 (TCF7L2) Variants With Type 2 Diabetes in a Finnish Sample.
Published in:
Diabetes, 2006, v. 55, n. 9, p. 2649, doi. 10.2337/db06-0341
By:
- Scott, Laura J.;
- Bonnycastle, Lori L.;
- Willer, Cristen J.;
- Sprau, Andrew G.;
- Jackson, Anne U.;
- Narisu, Narisu;
- Duren, William L.;
- Chines, Peter S.;
- Stringham, Heather M.;
- Erdos, Michael R.;
- Valle, Timo T.;
- Tuomilehto, Jaakko;
- Bergman, Richard N.;
- Mohlke, Karen L.;
- Collins, Francis S.;
- Boehnke, Michael
Publication type:
Article
Common Variants in Maturity-Onset Diabetes of the Young Genes Contribute to Risk of Type 2 Diabetes in Finns.
Published in:
Diabetes, 2006, v. 55, n. 9, p. 2534, doi. 10.2337/db06-0178
By:
- Bonnycastle, Lori L.;
- Willer, Cristen J.;
- Conneely, Karen N.;
- Jackson, Anne U.;
- Burrill, Cecily P.;
- Watanabe, Richard M.;
- Chines, Peter S.;
- Narisu, Narisu;
- Scott, Laura J.;
- Enloe, Sareena T.;
- Swift, Amy J.;
- Duren, William L.;
- Stringham, Heather M.;
- Erdos, Michael R.;
- Riebow, Nancy L.;
- Buchanan, Thomas A.;
- Valle, Timo T.;
- Tuomilehto, Jaakko;
- Bergman, Richard N.;
- Mohlke, Karen L.
Publication type:
Article
Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes.
Published in:
2004
By:
- Silander, Kaisa;
- Mohlke, Karen L.;
- Scott, Laura J.;
- Peck, Erin C.;
- Hollstein, Pablo;
- Skol, Andrew D.;
- Jackson, Anne U.;
- Deloukas, Panagiotis;
- Hunt, Sarah;
- Stavrides, George;
- Chines, Peter S.;
- Erdos, Michael R.;
- Narisu, Narisu;
- Conneely, Karen N.;
- Li, Chun;
- Fingerlin, Tasha E.;
- Dhanjal, Sharanjeet K.;
- Valle, Timo T.;
- Bergman, Richard N.;
- Tuomilehto, Jaakko
Publication type:
journal article
A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14.
Published in:
2004
By:
- Silander, Kaisa;
- Scott, Laura J.;
- Valle, Timo T.;
- Mohlke, Karen L.;
- Stringham, Heather M.;
- Wiles, Kerry R.;
- Duren, William L.;
- Doheny, Kimberly F.;
- Pugh, Elizabeth W.;
- Chines, Peter;
- Narisu, Narisu;
- White, Peggy P.;
- Fingerlin, Tasha E.;
- Jackson, Anne U.;
- Li, Chun;
- Ghosh, Soumitra;
- Magnuson, Victoria L.;
- Colby, Kimberly;
- Erdos, Michael R.;
- Hill, Jason E.
Publication type:
journal article
Variation in three single nucleotide polymorphisms in the calpain-10 gene not associated with type 2 diabetes in a large Finnish cohort.
Published in:
2002
By:
- Fingerlin, Tasha E.;
- Erdos, Michael R.;
- Watanabe, Richard M.;
- Wiles, Kerry R.;
- Stringham, Heather M.;
- Mohlke, Karen L.;
- Silander, Kaisa;
- Valle, Timo T.;
- Buchanan, Thomas A.;
- Tuomilehto, Jaakko;
- Bergman, Richard N.;
- Boehnke, Michael;
- Collins, Francis S.
Publication type:
journal article
The peroxisome proliferator-activated receptor-gamma2 Pro12A1a variant: association with type 2 diabetes and trait differences.
Published in:
2001
By:
- Douglas, Julie A.;
- Erdos, Michael R.;
- Watanabe, Richard M.;
- Braun, Andi;
- Johnston, Cristy L.;
- Oeth, Paul;
- Mohlke, Karen L.;
- Valle, Timo T.;
- Ehnholm, Christian;
- Buchanan, Thomas A.;
- Bergman, Richard N.;
- Collins, Francis S.;
- Boehnke, Michael;
- Douglas, J A;
- Erdos, M R;
- Watanabe, R M;
- Braun, A;
- Johnston, C L;
- Oeth, P;
- Mohlke, K L
Publication type:
journal article
Chromatin accessibility and gene expression during adipocyte differentiation identify context-dependent effects at cardiometabolic GWAS loci.
Published in:
PLoS Genetics, 2021, v. 17, n. 10, p. 1, doi. 10.1371/journal.pgen.1009865
By:
- Perrin, Hannah J.;
- Currin, Kevin W.;
- Vadlamudi, Swarooparani;
- Pandey, Gautam K.;
- Ng, Kenneth K.;
- Wabitsch, Martin;
- Laakso, Markku;
- Love, Michael I.;
- Mohlke, Karen L.
Publication type:
Article
Mediation analysis of multiple mediators with incomplete omics data.
Published in:
Genetic Epidemiology, 2023, v. 47, n. 1, p. 61, doi. 10.1002/gepi.22504
By:
- Kidd, John;
- Raulerson, Chelsea K.;
- Mohlke, Karen L.;
- Lin, Dan‐Yu
Publication type:
Article
Assessing exposure effects on gene expression.
Published in:
Genetic Epidemiology, 2020, v. 44, n. 6, p. 601, doi. 10.1002/gepi.22324
By:
- Reifeis, Sarah A.;
- Hudgens, Michael G.;
- Civelek, Mete;
- Mohlke, Karen L.;
- Love, Michael I.
Publication type:
Article
Tag SNP selection for Finnish individuals based on the CEPH Utah HapMap database.
Published in:
Genetic Epidemiology, 2006, v. 30, n. 2, p. 180, doi. 10.1002/gepi.20131
By:
- Cristen J. Willer;
- Laura J. Scott;
- Lori L. Bonnycastle;
- Anne U. Jackson;
- Peter Chines;
- Randall Pruim;
- Craig W. Bark;
- Ya‐Yu Tsai;
- Elizabeth W. Pugh;
- Kimberly F. Doheny;
- Leena Kinnunen;
- Karen L. Mohlke;
- Timo T. Valle;
- Richard N. Bergman;
- Jaakko Tuomilehto;
- Francis S. Collins;
- Michael Boehnke
Publication type:
Article
Genetic Variants Associated With Hidradenitis Suppurativa.
Published in:
JAMA Dermatology, 2023, v. 159, n. 9, p. 930, doi. 10.1001/jamadermatol.2023.2217
By:
- Sun, Quan;
- Broadaway, K. Alaine;
- Edmiston, Sharon N.;
- Fajgenbaum, Kristen;
- Miller-Fleming, Tyne;
- Westerkam, Linnea Lackstrom;
- Melendez-Gonzalez, Maria;
- Bui, Helen;
- Blum, Franklin R.;
- Levitt, Brandt;
- Lin, Lan;
- Hao, Honglin;
- Harris, Kathleen Mullan;
- Liu, Zhi;
- Thomas, Nancy E.;
- Cox, Nancy J.;
- Li, Yun;
- Mohlke, Karen L.;
- Sayed, Christopher J.
Publication type:
Article
Author Correction: Integration of human adipocyte chromosomal interactions with adipose gene expression prioritizes obesity-related genes from GWAS.
Published in:
Nature Communications, 2018, v. 9, p. 1, doi. 10.1038/s41467-018-05849-3
By:
- Pan, David Z.;
- Garske, Kristina M.;
- Alvarez, Marcus;
- Bhagat, Yash V.;
- Boocock, James;
- Nikkola, Elina;
- Zong Miao;
- Raulerson, Chelsea K.;
- Cantor, Rita M.;
- Civelek, Mete;
- Glastonbury, Craig A.;
- Small, Kerrin S.;
- Boehnke, Michael;
- Lusis, Aldons J.;
- Sinsheimer, Janet S.;
- Mohlke, Karen L.;
- Laakso, Markku;
- Pajukanta, Päivi;
- Ko, Arthur
Publication type:
Article
Integration of human adipocyte chromosomal interactions with adipose gene expression prioritizes obesity-related genes from GWAS.
Published in:
Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-03554-9
By:
- Pan, David Z.;
- Garske, Kristina M.;
- Alvarez, Marcus;
- Bhagat, Yash V.;
- Boocock, James;
- Nikkola, Elina;
- Zong Miao;
- Raulerson, Chelsea K.;
- Cantor, Rita M.;
- Civelek, Mete;
- Glastonbury, Craig A.;
- Small, Kerrin S.;
- Boehnke, Michael;
- Lusis, Aldons J.;
- Sinsheimer, Janet S.;
- Mohlke, Karen L.;
- Laakso, Markku;
- Pajukanta, Päivi;
- Ko, Arthur
Publication type:
Article
Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees.
Published in:
Clinical Genetics, 2019, v. 95, n. 5, p. 634, doi. 10.1111/cge.13515
By:
- Truong, Brittany T.;
- Yarza, Talitha K.L.;
- Bootpetch Roberts, Tori;
- Roberts, Susannah;
- Xu, Jonathan;
- Steritz, Matthew J.;
- Tobias‐Grasso, Celina A.M.;
- Azamian, Mahshid;
- Lalani, Seema R.;
- Mohlke, Karen L.;
- Lee, Nanette R.;
- Cutiongco‐de la Paz, Eva Maria;
- Reyes‐Quintos, Maria Rina T.;
- Santos‐Cortez, Regie Lyn P.;
- Chiong, Charlotte M.
Publication type:
Article
Evidence for Association between SH2B1 Gene Variants and Glycated Hemoglobin in Nondiabetic European American Young Adults: The Add Health Study.
Published in:
Annals of Human Genetics, 2016, v. 80, n. 5, p. 294, doi. 10.1111/ahg.12165
By:
- Lange, Leslie A.;
- Graff, Mariaelisa;
- Lange, Ethan M.;
- Young, Kristin L.;
- Richardson, Andrea S.;
- Mohlke, Karen L.;
- North, Kari E;
- Harris, Kathleen M;
- Gordon‐Larsen, Penny
Publication type:
Article
Removing reference mapping biases using limited or no genotype data identifies allelic differences in protein binding at diseaseassociated loci.
Published in:
BMC Medical Genomics, 2015, v. 8, n. 1, p. 1, doi. 10.1186/s12920-015-0117-x
By:
- Buchkovich, Martin L.;
- Eklund, Karl;
- Qing Duan;
- Yun Li;
- Mohlke, Karen L.;
- Furey, Terrence S.
Publication type:
Article
Removing reference mapping biases using limited or no genotype data identifies allelic differences in protein binding at disease-associated loci.
Published in:
BMC Medical Genomics, 2015, v. 8, n. 1, p. 43, doi. 10.1186/s12920-015-0117-x
By:
- Buchkovich, Martin L.;
- Eklund, Karl;
- Qing Duan;
- Yun Li;
- Mohlke, Karen L.;
- Furey, Terrence S.
Publication type:
Article
Identification of a Regulatory Variant That Binds FOXA1 and FOXA2 at the CDC123/CAMK1D Type 2 Diabetes GWAS Locus.
Published in:
PLoS Genetics, 2014, v. 10, n. 9, p. 1, doi. 10.1371/journal.pgen.1004633
By:
- Fogarty, Marie P.;
- Cannon, Maren E.;
- Vadlamudi, Swarooparani;
- Gaulton, Kyle J.;
- Mohlke, Karen L.
Publication type:
Article
Fine-Mapping and Initial Characterization of QT Interval Loci in African Americans.
Published in:
PLoS Genetics, 2012, v. 8, n. 8, p. 1, doi. 10.1371/journal.pgen.1002870
By:
- Avery, Christy L.;
- Sethupathy, Praveen;
- Buyske, Steven;
- He, Qianchuan;
- Lin, Dan-Yu;
- Arking, Dan E.;
- Carty, Cara L.;
- Duggan, David;
- Fesinmeyer, Megan D.;
- Hindorff, Lucia A.;
- Jeff, Janina M.;
- Klein, Liviu;
- Patton, Kristen K.;
- Peters, Ulrike;
- Shohet, Ralph V.;
- Sotoodehnia, Nona;
- Young, Alicia M.;
- Kooperberg, Charles;
- Haiman, Christopher A.;
- Mohlke, Karen L.
Publication type:
Article
Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.
Published in:
2022
By:
- Loh, Marie;
- Zhang, Weihua;
- Ng, Hong Kiat;
- Schmid, Katharina;
- Lamri, Amel;
- Tong, Lin;
- Ahmad, Meraj;
- Lee, Jung-Jin;
- Ng, Maggie C. Y.;
- Petty, Lauren E.;
- Spracklen, Cassandra N.;
- Takeuchi, Fumihiko;
- Islam, Md. Tariqul;
- Jasmine, Farzana;
- Kasturiratne, Anuradhani;
- Kibriya, Muhammad;
- Mohlke, Karen L.;
- Paré, Guillaume;
- Prasad, Gauri;
- Shahriar, Mohammad
Publication type:
Correction Notice
Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.
Published in:
Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-022-03248-5
By:
- Loh, Marie;
- Zhang, Weihua;
- Ng, Hong Kiat;
- Schmid, Katharina;
- Lamri, Amel;
- Tong, Lin;
- Ahmad, Meraj;
- Lee, Jung-Jin;
- Ng, Maggie C. Y.;
- Petty, Lauren E.;
- Spracklen, Cassandra N.;
- Takeuchi, Fumihiko;
- Islam, Md. Tariqul;
- Jasmine, Farzana;
- Kasturiratne, Anuradhani;
- Kibriya, Muhammad;
- Mohlke, Karen L.;
- Paré, Guillaume;
- Prasad, Gauri;
- Shahriar, Mohammad
Publication type:
Article
Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.
Published in:
Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-022-03248-5
By:
- Loh, Marie;
- Zhang, Weihua;
- Ng, Hong Kiat;
- Schmid, Katharina;
- Lamri, Amel;
- Tong, Lin;
- Ahmad, Meraj;
- Lee, Jung-Jin;
- Ng, Maggie C. Y.;
- Petty, Lauren E.;
- Spracklen, Cassandra N.;
- Takeuchi, Fumihiko;
- Islam, Md. Tariqul;
- Jasmine, Farzana;
- Kasturiratne, Anuradhani;
- Kibriya, Muhammad;
- Mohlke, Karen L.;
- Paré, Guillaume;
- Prasad, Gauri;
- Shahriar, Mohammad
Publication type:
Article
Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease.
Published in:
2019
By:
- Qiong Jia;
- Yi Han;
- Pin Huang;
- Woodward, Nicholas C.;
- Gukasyan, Janet;
- Kettunen, Johannes;
- Ala-Korpela, Mika;
- Anufrieva, Olga;
- Qin Wang;
- Perola, Markus;
- Raitakari, Olli;
- Lehtimäki, Terho;
- Viikari, Jorma;
- Järvelin, Marjo-Riitta;
- Boehnke, Michael;
- Laakso, Markku;
- Mohlke, Karen L.;
- Fiehn, Oliver;
- Zeneng Wang;
- Tang, W. H. Wilson
Publication type:
journal article
Associations of genetic variants in/near body mass index-associated genes with type 2 diabetes: a systematic meta-analysis.
Published in:
Clinical Endocrinology, 2014, v. 81, n. 5, p. 702, doi. 10.1111/cen.12428
By:
- Xi, Bo;
- Takeuchi, Fumihiko;
- Meirhaeghe, Aline;
- Kato, Norihiro;
- Chambers, John C.;
- Morris, Andrew P.;
- Cho, Yoon Shin;
- Zhang, Weihua;
- Mohlke, Karen L.;
- Kooner, Jaspal S.;
- Shu, Xiao Ou;
- Pan, Hongwei;
- Tai, E Shyong;
- Pan, Haiyan;
- Wu, Jer‐Yuarn;
- Zhou, Donghao;
- Chandak, Giriraj R.
Publication type:
Article
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Published in:
PLoS Genetics, 2017, v. 13, n. 10, p. 1, doi. 10.1371/journal.pgen.1007079
By:
- Davis, James P.;
- Huyghe, Jeroen R.;
- Locke, Adam E.;
- Jackson, Anne U.;
- Sim, Xueling;
- Stringham, Heather M.;
- Teslovich, Tanya M.;
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Article
Publisher Correction: Pla2g12b drives expansion of triglyceride-rich lipoproteins.
Published in:
2024
By:
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Publication type:
Correction Notice
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Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-46102-4
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Nonsynonymous variants and fatty liver disease.
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The causal effect of obesity on prediabetes and insulin resistance reveals the important role of adipose tissue in insulin resistance.
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GREGOR: evaluating global enrichment of trait-associated variants in epigenomic features using a systematic, data-driven approach.
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2015
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Product Review