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Estrogen Receptor β ( ESR2) Polymorphisms in Interaction With Estrogen Receptor α ( ESR1) and Insulin-Like Growth Factor I ( IGF1) Variants Influence the Risk of Fracture in Postmenopausal Women.
Published in:
Journal of Bone & Mineral Research, 2006, v. 21, n. 9, p. 1443, doi. 10.1359/jbmr.060605
By:
- Rivadeneira, Fernando;
- van Meurs, Joyce BJ;
- Kant, Jojanneke;
- Zillikens, M Carola;
- Stolk, Lisette;
- Beck, Thomas J;
- Arp, Pascal;
- Schuit, Stephanie CE;
- Hofman, Albert;
- Houwing-Duistermaat, Jeanine J;
- van Duijn, Cornelia M;
- van Leeuwen, Johannes PTM;
- Pols, Huibert AP;
- Uitterlinden, André G
Publication type:
Article
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.
Published in:
Nature Genetics, 2015, v. 47, n. 11, p. 1294, doi. 10.1038/ng.3412
By:
- Lunetta, Kathryn L;
- Pervjakova, Natalia;
- Chasman, Daniel I;
- Stolk, Lisette;
- Finucane, Hilary K;
- Bulik-Sullivan, Brendan;
- Esko, Tõnu;
- He, Chunyan;
- Altmaier, Elisabeth;
- Huffman, Jennifer E;
- Porcu, Eleonora;
- Vuckovic, Dragana;
- Corre, Tanguy;
- Mangino, Massimo;
- Smith, Albert V;
- Andrulis, Irene L;
- Barbieri, Caterina;
- Benitez, Javier;
- Boerwinkle, Eric;
- Bojesen, Stig E
Publication type:
Article
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.
Published in:
Nature Genetics, 2012, v. 44, n. 3, p. 260, doi. 10.1038/ng.1051
By:
- Stolk, Lisette;
- Perry, John R B;
- Chasman, Daniel I;
- He, Chunyan;
- Mangino, Massimo;
- Sulem, Patrick;
- Barbalic, Maja;
- Broer, Linda;
- Byrne, Enda M;
- Ernst, Florian;
- Esko, Tõnu;
- Franceschini, Nora;
- Gudbjartsson, Daniel F;
- Hottenga, Jouke-Jan;
- Kraft, Peter;
- McArdle, Patrick F;
- Porcu, Eleonora;
- Shin, So-Youn;
- Smith, Albert V;
- van Wingerden, Sophie
Publication type:
Article
Meta-analysis of genome-wide association data identifies two loci influencing age at menarche.
Published in:
Nature Genetics, 2009, v. 41, n. 6, p. 648, doi. 10.1038/ng.386
By:
- Perry, John R. B.;
- Stolk, Lisette;
- Franceschini, Nora;
- Lunetta, Kathryn L.;
- Guangju Zhai;
- McArdle, Patrick F.;
- Smith, Albert V.;
- Aspelund, Thor;
- Bandinelli, Stefania;
- Boerwinkle, Eric;
- Cherkas, Lynn;
- Eiriksdottir, Gudny;
- Estrada, Karol;
- Ferrucci, Luigi;
- Folsom, Aaron R.;
- Garcia, Melissa;
- Gudnason, Vilmundur;
- Hofman, Albert;
- Karasik, David;
- Kiel, Douglas P.
Publication type:
Article
Loci at chromosomes 13, 19 and 20 influence age at natural menopause.
Published in:
Nature Genetics, 2009, v. 41, n. 6, p. 645, doi. 10.1038/ng.387
By:
- Stolk, Lisette;
- Guangju Zhai;
- van Meurs, Joyce B. J.;
- Verbiest, Michael M. P. J.;
- Visser, Jenny A.;
- Estrada, Karol;
- Rivadeneira, Fernando;
- Williams, Frances M.;
- Cherkas, Lynn;
- Deloukas, Panos;
- Soranzo, Nicole;
- de Keyzer, Jules J.;
- Pop, Victor J. M.;
- Lips, Paul;
- Lebrun, Corinne E. I.;
- van der Schouw, Yvonne T.;
- Grobbee, Diederick E.;
- Witteman, Jacqueline;
- Hofman, Albert;
- Pols, Huibert A. P.
Publication type:
Article
Cross-ethnic meta-analysis of genetic variants for polycystic ovary syndrome.
Published in:
2013
By:
- Louwers, Yvonne V;
- Stolk, Lisette;
- Uitterlinden, André G;
- Laven, Joop S E
Publication type:
journal article
Variants in SULT2A1 Affect the DHEA Sulphate to DHEA Ratio in Patients With Polycystic Ovary Syndrome But Not the Hyperandrogenic Phenotype.
Published in:
2013
By:
- Louwers, Yvonne V;
- de Jong, Frank H;
- van Herwaarden, Nathalie A A;
- Stolk, Lisette;
- Fauser, Bart C J M;
- Uitterlinden, André G;
- Laven, Joop S E
Publication type:
Journal Article
Mendelian Randomization Study of Interleukin-6 in Chronic Obstructive Pulmonary Disease.
Published in:
Respiration, 2011, v. 82, n. 6, p. 530, doi. 10.1159/000332336
By:
- van Durme, Yannick M.T.A.;
- Lahousse, Lies;
- Verhamme, Katia M.C.;
- Stolk, Lisette;
- Eijgelsheim, Mark;
- Loth, Daan W.;
- Uitterlinden, Andre G.;
- Breteler, Monique M.B.;
- Joos, Guy F.;
- Hofman, Albert;
- Stricker, Bruno H.C.;
- Brusselle, Guy G.
Publication type:
Article
Genome-Wide Association Study in an Admixed Case Series Reveals IL12A as a New Candidate in Behçet Disease.
Published in:
PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0119085
By:
- Kappen, Jasper H.;
- Medina-Gomez, Carolina;
- Hagen, P. Martin van;
- Stolk, Lisette;
- Estrada, Karol;
- Rivadeneira, Fernando;
- Uitterlinden, Andre G.;
- Stanford, Miles R.;
- Ben-Chetrit, Eldat;
- Wallace, Graham R.;
- Soylu, Merih;
- Laar, Jan A.M. van
Publication type:
Article
Methylation of Migraine-Related Genes in Different Tissues of the Rat.
Published in:
PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0087616
By:
- Labruijere, Sieneke;
- Stolk, Lisette;
- Verbiest, Michael;
- de Vries, René;
- Garrelds, Ingrid M.;
- Eilers, Paul H. C.;
- Danser, A. H. Jan;
- Uitterlinden, André G.;
- MaassenVanDenBrink, Antoinette
Publication type:
Article
BMI-Associated Alleles Do Not Constitute Risk Alleles for Polycystic Ovary Syndrome Independently of BMI: A Case-Control Study.
Published in:
PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0087335
By:
- Louwers, Yvonne V.;
- Rayner, Nigel W.;
- Herrera, Blanca M.;
- Stolk, Lisette;
- Groves, Christopher J.;
- Barber, Thomas M.;
- Uitterlinden, Andre G.;
- Franks, Stephen;
- Laven, Joop S. E.;
- McCarthy, Mark I.
Publication type:
Article
DNA Methylation of IGF2DMR and H19 Is Associated with Fetal and Infant Growth: The Generation R Study.
Published in:
PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0081731
By:
- Bouwland-Both, Marieke I.;
- van Mil, Nina H.;
- Stolk, Lisette;
- Eilers, Paul H. C.;
- Verbiest, Michael M. P. J.;
- Heijmans, Bastiaan T.;
- Tiemeier, Henning;
- Hofman, Albert;
- Steegers, Eric A. P.;
- Jaddoe, Vincent W. V.;
- Steegers-Theunissen, Régine P. M.
Publication type:
Article
Epigenetic Profiles in Children with a Neural Tube Defect; A Case-Control Study in Two Populations.
Published in:
PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0078462
By:
- Stolk, Lisette;
- Bouwland-Both, Marieke I.;
- van Mill, Nina H.;
- Verbiest, Michael M. P. J.;
- Eilers, Paul H. C.;
- Zhu, Huiping;
- Suarez, Lucina;
- Uitterlinden, André G.;
- Steegers-Theunissen, Régine P. M.
Publication type:
Article
The Catechol-O-Methyltransferase Met158 Low-Activity Allele and Association with Nonvertebral Fracture Risk in Elderly Men
Published in:
Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 8, p. 3206, doi. 10.1210/jc.2006-2136
By:
- Stolk, Lisette;
- van Meurs, Joyce B. J.;
- Jhamai, Mila;
- Arp, Pascal P.;
- van Leeuwen, Johannes P. T.;
- Hofman, Albert;
- de Jong, Frank H.;
- Pols, Huibert A. P.;
- Uitterlinden, André G.
Publication type:
Article
Reproductive aging-associated common genetic variants and the risk of breast cancer.
Published in:
2012
By:
- He, Chunyan;
- Chasman, Daniel I;
- Dreyfus, Jill;
- Hwang, Shih-Jen;
- Ruiter, Rikje;
- Sanna, Serena;
- Buring, Julie E;
- Fernández-Rhodes, Lindsay;
- Franceschini, Nora;
- Hankinson, Susan E;
- Hofman, Albert;
- Lunetta, Kathryn L;
- Palmieri, Giuseppe;
- Porcu, Eleonora;
- Rivadeneira, Fernando;
- Rose, Lynda M;
- Splansky, Greta L;
- Stolk, Lisette;
- Uitterlinden, André G;
- Chanock, Stephen J
Publication type:
journal article
Low prevalence of NOD2 SNPs in Behcet's disease suggests protective association in Caucasians.
Published in:
Rheumatology, 2009, v. 48, n. 11, p. 1375, doi. 10.1093/rheumatology/kep292
By:
- Kappen, Jasper H.;
- Wallace, Graham R.;
- Stolk, Lisette;
- Rivadeneira, Fernando;
- Uitterlinden, Andre G.;
- van Daele, Paul L.A.;
- Laman, Jon D.;
- Kuijpers, Robert W.A.M.;
- Seerp Baarsma, Goitze;
- Stanford, Miles R.;
- Fortune, Farida;
- Madanat, Wafa;
- Martin van Hagen, Petrus;
- van Laar, Jan A.M.
Publication type:
Article
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass.
Published in:
Nature Communications, 2017, v. 8, n. 7, p. 1, doi. 10.1038/s41467-017-00031-7
By:
- Zillikens, M. Carola;
- Demissie, Serkalem;
- Yi-Hsiang Hsu;
- Yerges-Armstrong, Laura M.;
- Wen-Chi Chou;
- Stolk, Lisette;
- Livshits, Gregory;
- Broer, Linda;
- Johnson, Toby;
- Koller, Daniel L.;
- Kutalik, Zoltán;
- Luan, Jian’an;
- Malkin, Ida;
- Ried, Janina S.;
- Smith, Albert V.;
- Thorleifsson, Gudmar;
- Vandenput, Liesbeth;
- Jing Hua Zhao;
- Weihua Zhang;
- Aghdassi, Ali
Publication type:
Article
Corrigendum: Rare coding variants and X-linked loci associated with age at menarche.
Published in:
Nature Communications, 2015, v. 6, n. 12, p. 10257, doi. 10.1038/ncomms10257
By:
- Lunetta, Kathryn L.;
- Day, Felix R.;
- Sulem, Patrick;
- Ruth, Katherine S.;
- Tung, Joyce Y.;
- Hinds, David A.;
- Esko, Tõnu;
- Elks, Cathy E.;
- Altmaier, Elisabeth;
- He, Chunyan;
- Huffman, Jennifer E.;
- Mihailov, Evelin;
- Porcu, Eleonora;
- Robino, Antonietta;
- Rose, Lynda M.;
- Schick, Ursula M.;
- Stolk, Lisette;
- Teumer, Alexander;
- Thompson, Deborah J.;
- Traglia, Michela
Publication type:
Article
Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome.
Published in:
Nature Communications, 2015, v. 6, n. 9, p. 8464, doi. 10.1038/ncomms9464
By:
- Day, Felix R.;
- Hinds, David A.;
- Tung, Joyce Y.;
- Stolk, Lisette;
- Styrkarsdottir, Unnur;
- Saxena, Richa;
- Bjonnes, Andrew;
- Broer, Linda;
- Dunger, David B.;
- Halldorsson, Bjarni V.;
- Lawlor, Debbie A.;
- Laval, Guillaume;
- Mathieson, Iain;
- McCardle, Wendy L.;
- Louwers, Yvonne;
- Meun, Cindy;
- Ring, Susan;
- Scott, Robert A.;
- Sulem, Patrick;
- Uitterlinden, André G.
Publication type:
Article
Rare coding variants and X-linked loci associated with age at menarche.
Published in:
Nature Communications, 2015, v. 6, n. 8, p. 7756, doi. 10.1038/ncomms8756
By:
- Lunetta, Kathryn L.;
- Day, Felix R.;
- Sulem, Patrick;
- Ruth, Katherine S.;
- Tung, Joyce Y.;
- Hinds, David A.;
- Esko, Tõnu;
- Elks, Cathy E.;
- Altmaier, Elisabeth;
- He, Chunyan;
- Huffman, Jennifer E.;
- Mihailov, Evelin;
- Porcu, Eleonora;
- Robino, Antonietta;
- Rose, Lynda M.;
- Schick, Ursula M.;
- Stolk, Lisette;
- Teumer, Alexander;
- Thompson, Deborah J.;
- Traglia, Michela
Publication type:
Article
A genome-wide association study of early menopause and the combined impact of identified variants.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 7, p. 1465, doi. 10.1093/hmg/dds551
By:
- Perry, John R. B.;
- Corre, Tanguy;
- Esko, Tõnu;
- Chasman, Daniel I.;
- Fischer, Krista;
- Franceschini, Nora;
- He, Chunyan;
- Kutalik, Zoltan;
- Mangino, Massimo;
- Rose, Lynda M.;
- Vernon Smith, Albert;
- Stolk, Lisette;
- Sulem, Patrick;
- Weedon, Michael N.;
- Zhuang, Wei V.;
- Arnold, Alice;
- Ashworth, Alan;
- Bergmann, Sven;
- Buring, Julie E.;
- Burri, Andrea
Publication type:
Article
Genetic variation and bone mineral density in long-term adult survivors of childhood cancer.
Published in:
2016
By:
- den Hoed, Marissa A. H.;
- Pluijm, Saskia M. F.;
- Stolk, Lisette;
- Uitterlinden, André G.;
- Pieters, Rob;
- den Heuvel‐Eibrink, Marry M.;
- Uitterlinden, André G;
- van den Heuvel-Eibrink, Marry M
Publication type:
journal article
Genetic Determinants of Serum Testosterone Concentrations in Men.
Published in:
PLoS Genetics, 2011, v. 7, n. 10, p. 1, doi. 10.1371/journal.pgen.1002313
By:
- Ohlsson, Claes;
- Wallaschofski, Henri;
- Lunetta, Kathryn L.;
- Stolk, Lisette;
- Perry, John R. B.;
- Koster, Annemarie;
- Petersen, Ann-Kristin;
- Eriksson, Joel;
- Lehtimäki, Terho;
- Huhtaniemi, Ilpo T.;
- Hammond, Geoffrey L.;
- Maggio, Marcello;
- Coviello, Andrea D.;
- Ferrucci, Luigi;
- Heier, Margit;
- Hofman, Albert;
- Holliday, Kate L.;
- Jansson, John-Olov;
- Kähönen, Mika;
- Karasik, David
Publication type:
Article
Eight Common Genetic Variants Associated with Serum DHEAS Levels Suggest a Key Role in Ageing Mechanisms.
Published in:
PLoS Genetics, 2011, v. 7, n. 4, p. 1, doi. 10.1371/journal.pgen.1002025
By:
- Guangju Zhai;
- Teumer, Alexander;
- Stolk, Lisette;
- Perry, John R. B.;
- Vandenput, Liesbeth;
- Coviello, Andrea D.;
- Koster, Annemarie;
- Bell, Jordana T.;
- Bhasin, Shalender;
- Eriksson, Joel;
- Eriksson, Anna;
- Ernst, Florian;
- Ferrucci, Luigi;
- Frayling, Timothy M.;
- Glass, Daniel;
- Grundberg, Elin;
- Haring, Robin;
- Hedman, Asa K.;
- Hofman, Albert;
- Kiel, Douglas P.
Publication type:
Article
Meta-Analysis of Genome-Wide Scans for Human Adult Stature Identifies Novel Loci and Associations with Measures of Skeletal Frame Size.
Published in:
PLoS Genetics, 2009, v. 5, n. 4, p. 1, doi. 10.1371/journal.pgen.1000445
By:
- Soranzo, Nicole;
- Rivadeneira, Fernando;
- Chinappen-Horsley, Usha;
- Malkina, Ida;
- Richards, J. Brent;
- Hammond, Naomi;
- Stolk, Lisette;
- Nica, Alexandra;
- Inouye, Michael;
- Hofman, Albert;
- Stephens, Jonathan;
- Wheeler, Eleanor;
- Arp, Pascal;
- Gwilliam, Rhian;
- Jhamai, P. Mila;
- Potter, Simon;
- Chaney, Amy;
- Ghori, Mohammed J. R.;
- Ravindrarajah, Radhi;
- Ermakov, Sergey
Publication type:
Article
A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.
Published in:
Human Molecular Genetics, 2009, v. 18, n. 18, p. 3516, doi. 10.1093/hmg/ddp296
By:
- Estrada, Karol;
- Krawczak, Michael;
- Schreiber, Stefan;
- van Duijn, Kate;
- Stolk, Lisette;
- van Meurs, Joyce B.J.;
- Liu, Fan;
- Penninx, Brenda W.J.H.;
- Smit, Jan H.;
- Vogelzangs, Nicole;
- Hottenga, Jouke Jan;
- Willemsen, Gonneke;
- de Geus, Eco J.C.;
- Lorentzon, Mattias;
- von Eller-Eberstein, Huberta;
- Lips, Paul;
- Schoor, Natascha;
- Pop, Victor;
- de Keijzer, Jules;
- Hofman, Albert
Publication type:
Article
Prenatal parental tobacco smoking, gene specific DNA methylation, and newborns size: the Generation R study.
Published in:
Clinical Epigenetics, 2015, v. 7, n. 1, p. 1, doi. 10.1186/s13148-015-0115-z
By:
- Bouwland-Both, Marieke I.;
- van Mil, Nina H.;
- Tolhoek, Catharina P.;
- Stolk, Lisette;
- Eilers, Paul H. C.;
- Verbiest, Michael M. P. J.;
- Heijmans, Bastiaan T.;
- Uitterlinden, André G.;
- Hofman, Albert;
- van Ijzendoorn, Marinus H.;
- Duijts, Liesbeth;
- de Jongste, Johan C.;
- Tiemeier, Henning;
- Steegers, Eric A. P.;
- Jaddoe, Vincent W. V.;
- Steegers-Theunissen, Régine P. M.
Publication type:
Article
Tobacco smoking is associated with methylation of genes related to coronary artery disease.
Published in:
Clinical Epigenetics, 2015, v. 7, n. 1, p. 1, doi. 10.1186/s13148-015-0088-y
By:
- Steenaard, Rebecca V.;
- Ligthart, Symen;
- Stolk, Lisette;
- Peters, Marjolein J.;
- van Meurs, Joyce B.;
- Uitterlinden, Andre G.;
- Hofman, Albert;
- Franco, Oscar H.;
- Dehghan, Abbas
Publication type:
Article
Identification of Genetic Loci Associated With Helicobacter pylori Serologic Status.
Published in:
JAMA: Journal of the American Medical Association, 2013, v. 309, n. 18, p. 1992, doi. 10.1001/jama.2013.4350
By:
- Mayerle, Julia;
- den Hoed, Caroline M.;
- Schurmann, Claudia;
- Stolk, Lisette;
- Homuth, Georg;
- Peters, Marjolein J.;
- Capelle, Lisette G.;
- Zimmermann, Kathrin;
- Rivadeneira, Fernando;
- Gruska, Sybille;
- Völzke, Henry;
- de Vries, Annemarie C.;
- Völker, Uwe;
- Teumer, Alexander;
- van Meurs, Joyce B. J.;
- Steinmetz, Ivo;
- Nauck, Matthias;
- Ernst, Florian;
- Weiss, Frank-Ulrich;
- Hofman, Albert
Publication type:
Article
High bone mineral density and fracture risk in type 2 diabetes as skeletal complications of inadequate glucose control: the Rotterdam Study.
Published in:
2013
By:
- Oei, Ling;
- Zillikens, M Carola;
- Dehghan, Abbas;
- Buitendijk, Gabriëlle H S;
- Castaño-Betancourt, Martha C;
- Estrada, Karol;
- Stolk, Lisette;
- Oei, Edwin H G;
- van Meurs, Joyce B J;
- Janssen, Joseph A M J L;
- Hofman, Albert;
- van Leeuwen, Johannes P T M;
- Witteman, Jacqueline C M;
- Pols, Huibert A P;
- Uitterlinden, André G;
- Klaver, Caroline C W;
- Franco, Oscar H;
- Rivadeneira, Fernando
Publication type:
journal article
High Bone Mineral Density and Fracture Risk in Type 2 Diabetes as Skeletal Complications of Inadequate Glucose Control.
Published in:
Diabetes Care, 2013, v. 36, n. 6, p. 1619, doi. 10.2337/dc12-1188
By:
- OEI, LING;
- ZILLIKENS, M. CAROLA;
- DEHGHAN, ABBAS;
- BUITENDIJK, GABRIËLLE H. S.;
- CASTAÑO-BETANCOURT, MARTHA C.;
- ESTRADA, KAROL;
- STOLK, LISETTE;
- OEI, EDWIN H. G.;
- VAN MEURS, JOYCE B. J.;
- JANSSEN, JOSEPH A. M. J. L.;
- HOFMAN, ALBERT;
- VAN LEEUWEN, JOHANNES P. T. M.;
- WITTEMAN, JACQUELINE C. M.;
- POLS, HUIBERT A. P.;
- UITTERLINDEN, ANDRÉ G.;
- KLAVER, CAROLINE C. W.;
- FRANCO, OSCAR H.;
- RIVADENEIRA, FERNANDO
Publication type:
Article
Genetically defined elevated homocysteine levels do not result in widespread changes of DNA methylation in leukocytes.
Published in:
PLoS ONE, 2017, v. 12, n. 10, p. 1, doi. 10.1371/journal.pone.0182472
By:
- Mandaviya, Pooja R.;
- Joehanes, Roby;
- Aïssi, Dylan;
- Kühnel, Brigitte;
- Marioni, Riccardo E.;
- Truong, Vinh;
- Stolk, Lisette;
- Beekman, Marian;
- Bonder, Marc Jan;
- Franke, Lude;
- Gieger, Christian;
- Huan, Tianxiao;
- Ikram, M. Arfan;
- Kunze, Sonja;
- Liang, Liming;
- Lindemans, Jan;
- Liu, Chunyu;
- McRae, Allan F.;
- Mendelson, Michael M.;
- Müller-Nurasyid, Martina
Publication type:
Article
Common genetic variation in the Estrogen Receptor Beta (ESR2) gene and osteoarthritis: results of a meta-analysis.
Published in:
BMC Medical Genetics, 2010, v. 11, p. 164, doi. 10.1186/1471-2350-11-164
By:
- Kerkhof, Hanneke J. M.;
- Meulenbelt, Ingrid;
- Carr, Andrew;
- Gonzalez, Antonio;
- Hart, Deborah;
- Hofman, Albert;
- Kloppenburg, Margreet;
- Lane, Nancy E.;
- Loughlin, John;
- Nevitt, Michael C.;
- Pols, Huibert A. P.;
- Rivadeneira, Fernando;
- Slagboom, Eline P.;
- Spector, Tim D.;
- Stolk, Lisette;
- Tsezou, Aspasia;
- Uitterlinden, André G.;
- Valdes, Ana M.;
- van Meurs, Joyce B. J.
Publication type:
Article

Found: 33

Estrogen Receptor β ( ESR2) Polymorphisms in Interaction With Estrogen Receptor α ( ESR1) and Insulin-Like Growth Factor I ( IGF1) Variants Influence the Risk of Fracture in Postmenopausal Women.

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.

Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.

Meta-analysis of genome-wide association data identifies two loci influencing age at menarche.

Loci at chromosomes 13, 19 and 20 influence age at natural menopause.

Cross-ethnic meta-analysis of genetic variants for polycystic ovary syndrome.

Variants in SULT2A1 Affect the DHEA Sulphate to DHEA Ratio in Patients With Polycystic Ovary Syndrome But Not the Hyperandrogenic Phenotype.

Mendelian Randomization Study of Interleukin-6 in Chronic Obstructive Pulmonary Disease.

Genome-Wide Association Study in an Admixed Case Series Reveals IL12A as a New Candidate in Behçet Disease.

Methylation of Migraine-Related Genes in Different Tissues of the Rat.

BMI-Associated Alleles Do Not Constitute Risk Alleles for Polycystic Ovary Syndrome Independently of BMI: A Case-Control Study.

DNA Methylation of <i>IGF2DMR</i> and <i>H19</i> Is Associated with Fetal and Infant Growth: The Generation R Study.

Epigenetic Profiles in Children with a Neural Tube Defect; A Case-Control Study in Two Populations.

The Catechol-O-Methyltransferase Met<sup>158</sup> Low-Activity Allele and Association with Nonvertebral Fracture Risk in Elderly Men

Reproductive aging-associated common genetic variants and the risk of breast cancer.

Low prevalence of NOD2 SNPs in Behcet's disease suggests protective association in Caucasians.

Large meta-analysis of genome-wide association studies identifies five loci for lean body mass.

Corrigendum: Rare coding variants and X-linked loci associated with age at menarche.

Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome.

Rare coding variants and X-linked loci associated with age at menarche.

A genome-wide association study of early menopause and the combined impact of identified variants.

Genetic variation and bone mineral density in long-term adult survivors of childhood cancer.

Genetic Determinants of Serum Testosterone Concentrations in Men.

Eight Common Genetic Variants Associated with Serum DHEAS Levels Suggest a Key Role in Ageing Mechanisms.

Meta-Analysis of Genome-Wide Scans for Human Adult Stature Identifies Novel Loci and Associations with Measures of Skeletal Frame Size.

A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.

Prenatal parental tobacco smoking, gene specific DNA methylation, and newborns size: the Generation R study.

Tobacco smoking is associated with methylation of genes related to coronary artery disease.

Identification of Genetic Loci Associated With Helicobacter pylori Serologic Status.

High bone mineral density and fracture risk in type 2 diabetes as skeletal complications of inadequate glucose control: the Rotterdam Study.

High Bone Mineral Density and Fracture Risk in Type 2 Diabetes as Skeletal Complications of Inadequate Glucose Control.

Genetically defined elevated homocysteine levels do not result in widespread changes of DNA methylation in leukocytes.

Common genetic variation in the Estrogen Receptor Beta (ESR2) gene and osteoarthritis: results of a meta-analysis.