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1. Full Text Contribution of Four Polymorphisms in Renin-Angiotensin-Aldosterone-Related Genes to Hypertension in a Thai Population
by Charoen, Pimphen and Eu-ahsunthornwattana, Jakris and Thongmung, Nisakron and Jose, Pedro A and Sritara, Piyamitr and Vathesatogkit, Prin and Kitiyakara, Chagriya
International journal of hypertension, ISSN 2090-0384, 8/2019, Volume 2019, pp. 4861081 - 8
Cardiac & Cardiovascular Systems | Peripheral Vascular Disease | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Hypertension | Corticosteroids | Genes | Angiotensin | Cytochrome P-450 | Genetic aspects | Research | Aldosterone | Genetic polymorphisms | Enzymes | Disease | Population | Employees | Genetics | Genomes | Blood pressure | Polymorphism
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2. Full Text Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux
by Darlow, John M and Darlay, Rebecca and Dobson, Mark G and Stewart, Aisling and Charoen, Pimphen and Southgate, Jennifer and Baker, Simon C and Xu, Yaobo and Hunziker, Manuela and Lambert, Heather J and Green, Andrew J and Santibanez-Koref, Mauro and Sayer, John A and Goodship, Timothy H. J and Puri, Prem and Woolf, Adrian S and Kenda, Rajko B and Barton, David E and Cordell, Heather J
Scientific reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 14595 - 13
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Vesico-Ureteral Reflux - genetics | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Genetic Testing | Humans | Cells, Cultured | Male | Genetic Loci | Case-Control Studies | Family | Female | Chromosomes, Human, Pair 10 | Genetic Linkage | Dysplasia | Kidneys | Etiology | Renal failure | Association analysis | Population studies | Genomes | Urinary tract | Children | Linkage analysis | Kidney transplantation
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3. Full Text Mendelian Randomisation study of the influence of EGFR on coronary heart disease
by Charoen, Pimphen and Nitsch, Dorothea and Engmann, Jorgen and Shah, Tina and White, Jonathan and Zabaneh, Delilah and Jefferis, Barbara and Wannamethee, Goya and Whincup, Peter and Cassidy, Amy Mulick and Gaunt, Tom and Day, Ian and McLachlan, Stela and Price, Jacqueline and Kumari, Meena and Kivimaki, Mika and Brunner, Eric and Langenberg, Claudia and Ben-Shlomo, Yoav and Hingorani, Aroon and Whittaker, John and Pablo Casas, Juan and Dudbridge, Frank and UCLEB Consortium and the UCLEB Consortium
Scientific reports, ISSN 2045-2322, 06/2016, Volume 6, Issue 1, pp. 28514 - 28514
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genome-Wide Association Study | Kidney - metabolism | Coronary Disease - metabolism | Humans | Risk Factors | Mendelian Randomization Analysis | Coronary Disease - physiopathology | Glomerular Filtration Rate - genetics | Polymorphism, Single Nucleotide | Odds Ratio | Kidney - physiopathology | Index Medicus
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4. Full Text Publisher Correction: Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux
by Darlow, John M and Darlay, Rebecca and Dobson, Mark G and Stewart, Aisling and Charoen, Pimphen and Southgate, Jennifer and Baker, Simon C and Xu, Yaobo and Hunziker, Manuela and Lambert, Heather J and Green, Andrew J and Santibanez-Koref, Mauro and Sayer, John A and Goodship, Timothy H J and Puri, Prem and Woolf, Adrian S and Kenda, Rajko B and Barton, David E and Cordell, Heather J
Scientific reports, ISSN 2045-2322, 01/2018, Volume 8, Issue 1, pp. 459 - 459
Genomes
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5. Full Text TTC12-ANKK1-DRD2 and CHRNA5-CHRNA3-CHRNB4 Influence Different Pathways Leading to Smoking Behavior from Adolescence to Mid-Adulthood
by Ducci, Francesca and Kaakinen, Marika and Pouta, Anneli and Hartikainen, Anna-Liisa and Veijola, Juha and Isohanni, Matti and Charoen, Pimphen and Coin, Lachlan and Hoggart, Clive and Ekelund, Jesper and Peltonen, Leena and Freimer, Nelson and Elliott, Paul and Schumann, Gunter and Järvelin, Marjo-Riitta
Biological psychiatry (1969), ISSN 0006-3223, 2011, Volume 69, Issue 7, pp. 650 - 660
Psychiatry | Adolescence | CHRNA3 | CHRNB4 | nicotine | TTC12 | CHRNA5 | gene | smoking | ANKK1 | DRD2 | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Genetic Predisposition to Disease | Gene Frequency | Humans | Middle Aged | Risk Factors | Community Health Planning | Protein-Serine-Threonine Kinases - genetics | Genotype | Male | Smoking - genetics | Chromosomes, Human, Pair 11 - genetics | Receptors, Dopamine D2 - genetics | Proteins - genetics | Models, Biological | Adolescent | Finland | Sex Factors | Statistics, Nonparametric | Female | Retrospective Studies | Longitudinal Studies | Receptors, Nicotinic - genetics | Index Medicus | adolescence
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6. Full Text Erratum: Publisher Correction: Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux (Scientific reports (2017) 7 1 (14595))
by Darlow, John M and Darlay, Rebecca and Dobson, Mark G and Stewart, Aisling and Charoen, Pimphen and Southgate, Jennifer and Baker, Simon C and Xu, Yaobo and Hunziker, Manuela and Lambert, Heather J and Green, Andrew J and Santibanez-Koref, Mauro and Sayer, John A and Goodship, Timothy H J and Puri, Prem and Woolf, Adrian S and Kenda, Rajko B and Barton, David E and Cordell, Heather J
Scientific reports, 01/2018, Volume 8, Issue 1, p. 459
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7. Full Text A neurobiological pathway to smoking in adolescence: TTC12-ANKK1-DRD2 variants and reward response
by Macare, Christine and Ducci, Francesca and Zhang, Yuning and Ruggeri, Barbara and Jia, Tianye and Kaakinen, Marika and Kalsi, Gursharan and Charoen, Pimphen and Casoni, Filippo and Peters, Jan and Bromberg, Uli and Hill, Matthew and Buxton, Jessica and Blakemore, Alexandra and Veijola, Juha and Büchel, Christian and Banaschewski, Tobias and Bokde, Arun L.W and Conrod, Patricia and Flor, Herta and Frouin, Vincent and Gallinat, Jürgen and Garavan, Hugh and Gowland, Penny A and Heinz, Andreas and Ittermann, Bernd and Lathrop, Mark and Martinot, Jean-Luc and Paus, Tomáš and Desrivières, Sylvane and Munafò, Marcus and Järvelin, Marjo-Riitta and Schumann, Gunter and The IMAGEN Consortium and IMAGEN Consortium
European neuropsychopharmacology, ISSN 0924-977X, 10/2018, Volume 28, Issue 10, pp. 1103 - 1114
fMRI | Genetics | Risk taking | IMAGEN-ALSPAC-NFBC | Meta-analysis | Smoking | Neurosciences | Clinical Neurology | Life Sciences & Biomedicine | Pharmacology & Pharmacy | Neurosciences & Neurology | Psychiatry | Science & Technology | Brain - diagnostic imaging | Behavior, Addictive - diagnostic imaging | Genetic Association Studies | Behavior, Addictive - genetics | Brain - physiopathology | Humans | Protein-Serine-Threonine Kinases - genetics | Anticipation, Psychological - physiology | Male | Smoking - genetics | Receptors, Dopamine D2 - genetics | Genetic Variation | Proteins - genetics | Magnetic Resonance Imaging | Cotinine - blood | Adolescent Behavior - psychology | Smoking - physiopathology | Adolescent | Female | Adolescent Behavior - physiology | Behavior, Addictive - psychology | Reward | Smoking - psychology | Behavior, Addictive - physiopathology | Analysis | Dopamine receptors | Index Medicus
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8. Full Text Robust approaches for performing meta-analysis of genome-wide association studies to identify single nucleotide polymorphisms and copy number variations associated with complex traits
by Charoen, Pimphen
2013
614
Dissertation
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9. Full Text Erratum: Whole-genome sequence-based analysis of thyroid function (Nature Communications (2015) 6(5681) 10.1038/ncomms6681)
by Taylor, Peter N and Porcu, Eleonora and Chew, Shelby and Campbell, Purdey J and Traglia, Michela and Brown, Suzanne J and Mullin, Benjamin H and Shihab, Hashem A and Min, Josine and Walter, Klaudia and Memari, Yasin and Huang, Jie and Barnes, Michael R and Beilby, John P and Charoen, Pimphen and Danecek, Petr and Dudbridge, Frank and Forgetta, Vincenzo and Greenwood, Celia and Grundberg, Elin and Johnson, Andrew D and Hui, Jennie and Lim, Ee M and McCarthy, Shane and Muddyman, Dawn and Panicker, Vijay and Perry, John R.B and Bell, Jordana T and Yuan, Wei and Relton, Caroline and Gaunt, Tom and Schlessinger, David and Abecasis, Goncalo and Cucca, Francesco and Surdulescu, Gabriela L and Woltersdorf, Wolfram and Zeggini, Eleftheria and Zheng, Hou-Feng and Toniolo, Daniela and Dayan, Colin M and Naitza, Silvia and Walsh, John P and Spector, Tim and Smith, George Davey and Durbin, Richard and Richards, J. Brent and Sanna, Serena and Soranzo, Nicole and Timpson, Nicholas J and Wilson, Scott G
Nature communications, 05/2015, Volume 6
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10. Full Text Glucocorticoid receptor (NR3C1) gene polymorphisms and onset of alcohol abuse in adolescents
by Desrivières, Sylvane and Lourdusamy, Anbarasu and Müller, Christian and Ducci, Francesca and Wong, Cybele P and Kaakinen, Marika and Pouta, Anneli and Hartikainen, Anna‐Liisa and Isohanni, Matti and Charoen, Pimphen and Peltonen, Leena and Freimer, Nelson and Elliott, Paul and Jarvelin, Marjo‐Riitta and Schumann, Gunter
Addiction biology, ISSN 1355-6215, 07/2011, Volume 16, Issue 3, pp. 510 - 513
alcohol | adolescent | glucocorticoid receptor | polymorphism | Addiction | NR3C1 | Alcohol | Adolescent | Glucocorticoid receptor | Polymorphism | Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Substance Abuse | Science & Technology | Alcoholic Intoxication - genetics | Genetic Predisposition to Disease - genetics | Genetic Testing | Prospective Studies | Humans | Male | Alcohol Drinking - genetics | Phenotype | Age of Onset | Alleles | Finland | Receptors, Glucocorticoid - genetics | Sex Factors | Polymorphism, Single Nucleotide - genetics | Alcoholism - genetics | Female | Polymorphism, Genetic - genetics | Cohort Studies | Corticosteroids | Youth | Alcohol and youth | Genetic aspects | Teenagers | Drinking of alcoholic beverages | Public health | Alcohol use | Steroids | Index Medicus
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11. Full Text Erratum: Whole-genome sequence-based analysis of thyroid function
by Taylor, Peter N and Porcu, Eleonora and Chew, Shelby and Campbell, Purdey J and Traglia, Michela and Brown, Suzanne J and Mullin, Benjamin H and Shihab, Hashem A and Min, Josine and Walter, Klaudia and Memari, Yasin and Huang, Jie and Barnes, Michael R and Beilby, John P and Charoen, Pimphen and Danecek, Petr and Dudbridge, Frank and Forgetta, Vincenzo and Greenwood, Celia and Grundberg, Elin and Johnson, Andrew D and Hui, Jennie and Lim, Ee M and McCarthy, Shane and Muddyman, Dawn and Panicker, Vijay and Perry, John R B and Bell, Jordana T and Yuan, Wei and Relton, Caroline and Gaunt, Tom and Schlessinger, David and Abecasis, Goncalo and Cucca, Francesco and Surdulescu, Gabriela L and Woltersdorf, Wolfram and Zeggini, Eleftheria and Zheng, Hou-Feng and Toniolo, Daniela and Dayan, Colin M and Naitza, Silvia and Walsh, John P and Spector, Tim and Smith, George Davey and Durbin, Richard and Richards, J Brent and Sanna, Serena and Soranzo, Nicole and Timpson, Nicholas J and Wilson, Scott G and UK10K Consortium and the UK10K Consortium
Nature communications, ISSN 2041-1723, 05/2015, Volume 6, Issue 1, pp. 7172 - 7172
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12. Full Text TTC12-ANKK1-DRD2 and CHRNAS-CHRNA3-CHRN84 Influence Different Pathways Leading to Smoking Behavior from Adolescence to Mid-Adulthood
: Reduced Behavioral Flexibility in Addiction
by DUCCI, Francesca and KAAKINEN, Marika and PELTONEN, Leena and FREIMER, Nelson and ELLIOTT, Paul and SCHUMANN, Gunter and JÄRVELIN, Marjo-Riitta and POUTA, Anneli and HARTIKAINEN, Anna-Liisa and VEIJOLA, Juha and ISOHANNI, Matti and CHAROEN, Pimphen and COIN, Lachlan and HOGGART, Clive and EKELUND, Jesper
Biological psychiatry (1969), ISSN 0006-3223, 2011, Volume 69, Issue 7, pp. 650 - 660
Toxicology | Psychology. Psychoanalysis. Psychiatry | Adult and adolescent clinical studies | Psychopathology. Psychiatry | Addictive behaviors | Tobacco smoking | Biological and medical sciences | Medical sciences | Tobacco, tobacco smoking
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13. Full Text Erratum: Common variants at 12q15 and 12q24 are associated with infant head circumference (Nature Genetics (2012) 44 (532-538))
by Taal, H Rob and St Pourcain, Beate and Thiering, Elisabeth and Das, Shikta and Mook-Kanamori, Dennis O and Warrington, Nicole M and Kaakinen, Marika and Kreiner-Møller, Eskil and Bradfield, Jonathan P and Freathy, Rachel M and Geller, Frank and Guxens, Mònica and Cousminer, Diana L and Kerkhof, Marjan and Timpson, Nicholas J and Ikram, M Arfan and Beilin, Lawrence J and Bønnelykke, Klaus and Buxton, Jessica L and Charoen, Pimphen and Chawes, Bo Lund Krogsgaard and Eriksson, Johan and Evans, David M and Hofman, Albert and Kemp, John P and Kim, Cecilia E and Klopp, Norman and Lahti, Jari and Lye, Stephen J and McMahon, George and Mentch, Frank D and Müller-Nurasyid, Martina and O'Reilly, Paul F and Prokopenko, Inga and Rivadeneira, Fernando and Steegers, Eric A. P and Sunyer, Jordi and Tiesler, Carla and Yaghootkar, Hanieh and Breteler, Monique M. B and Debette, Stéphanie and Fornage, Myriam and Gudnason, Vilmundur and Launer, Lenore J and Van Der Lugt, Aad and Mosley Jr, Thomas H and Seshadri, Sudha and Smith, Albert V and Vernooij, Meike W and Blakemore, Alexandra I. F and Chiavacci, Rosetta M and Feenstra, Bjarke and Fernandez-Banet, Julio and Grant, Struan F. A and Hartikainen, Anna-Liisa and Van Der Heijden, Albert J and Iñiguez, Carmen and Lathrop, Mark and McArdle, Wendy L and Mølgaard, Anne and Newnham, John P and Palmer, Lyle J and Palotie, Aarno and Pouta, Annneli and Ring, Susan M and Sovio, Ulla and Standl, Marie and Uitterlinden, Andre G and Wichmann, H-Erich and Vissing, Nadja Hawwa and DeCarli, Charles and Van Duijn, Cornelia M and McCarthy, Mark I and Koppelman, Gerard H and Estivill, Xavier and Hattersley, Andrew T and Melbye, Mads and Bisgaard, Hans and Pennell, Craig E and Widen, Elisabeth and Hakonarson, Hakon and Smith, George Davey and Heinrich, Joachim and Jarvelin, Marjo-Riitta and Jaddoe, Vincent W. V
Nature genetics, ISSN 1061-4036, 06/2013, Volume 45, Issue 6, p. 713
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14. Full Text Common variants at 12q15 and 12q24 are associated with infant head circumference (vol 44, pg 532, 2012)
by Taal, H. Rob and St Pourcain, Beate and Thiering, Elisabeth and Das, Shikta and Mook-Kanamori, Dennis O and Warrington, Nicole M and Kaakinen, Marika and Kreiner-Moller, Eskil and Bradfield, Jonathan P and Freathy, Rachel M and Geller, Frank and Guxens, Monica and Cousminer, Diana L and Kerkhof, Marjan and Timpson, Nicholas J and Ikram, M. Arfan and Beilin, Lawrence J and Bonnelykke, Klaus and Buxton, Jessica L and Charoen, Pimphen and Chawes, Bo Lund Krogsgaard and Eriksson, Johan and Evans, David M and Hofman, Albert and Kemp, John P and EKim, Cecilia and Klopp, Norman and Lahti, Jari and Lye, Stephen J and McMahon, George and Mentch, Frank D and Mueller-Nurasyid, Martina and O'Reilly, Paul F and Prokopenko, Inga and Rivadeneira, Fernando and Steegers, Eric A. P and Sunyer, Jordi and Tiesler, Carla and Yaghootkar, Hanieh and Breteler, Monique M. B and Debette, Stephanie and Fornage, Myriam and Gudnason, Vilmundur and Launer, Lenore J and van der Lugt, Aad and Mosley, Thomas H and Seshai, Sudha and Smith, Albert V and Vernooij, Meike W and Koppelman, Gerard H and EAGLE Consortium and EGG Consortium and CHARGE Consortium
Nature genetics, ISSN 1061-4036, 06/2013, Volume 45, Issue 6, pp. 713 - 713
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology
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15. Full Text Erratum: Common variants at 12q15 and 12q24 are associated with infant head circumference
by Taal, H Rob and St Pourcain, Beate and Thiering, Elisabeth and Das, Shikta and Mook-Kanamori, Dennis O and Warrington, Nicole M and Kaakinen, Marika and Kreiner-Møller, Eskil and Bradfield, Jonathan P and Freathy, Rachel M and Geller, Frank and Guxens, Mònica and Cousminer, Diana L and Kerkhof, Marjan and Timpson, Nicholas J and Ikram, M Arfan and Beilin, Lawrence J and Bønnelykke, Klaus and Buxton, Jessica L and Charoen, Pimphen and Chawes, Bo Lund Krogsgaard and Eriksson, Johan and Evans, David M and Hofman, Albert and Kemp, John P and Kim, Cecilia E and Klopp, Norman and Lahti, Jari and Lye, Stephen J and McMahon, George and Mentch, Frank D and Müller-Nurasyid, Martina and O'Reilly, Paul F and Prokopenko, Inga and Rivadeneira, Fernando and Steegers, Eric A P and Sunyer, Jordi and Tiesler, Carla and Yaghootkar, Hanieh and Breteler, Monique M B and Debette, Stéphanie and Fornage, Myriam and Gudnason, Vilmundur and Launer, Lenore J and van der Lugt, Aad and Mosley, Thomas H and Seshadri, Sudha and Smith, Albert V and Vernooij, Meike W and Blakemore, Alexandra I F and Chiavacci, Rosetta M and Feenstra, Bjarke and Fernandez-Banet, Julio and Grant, Struan F A and Hartikainen, Anna-Liisa and van der Heijden, Albert J and Iñiguez, Carmen and Lathrop, Mark and McArdle, Wendy L and Mølgaard, Anne and Newnham, John P and Palmer, Lyle J and Palotie, Aarno and Pouta, Annneli and Ring, Susan M and Sovio, Ulla and Standl, Marie and Uitterlinden, Andre G and Wichmann, H-Erich and Vissing, Nadja Hawwa and DeCarli, Charles and van Duijn, Cornelia M and McCarthy, Mark I and Koppelman, Gerard H and Estivill, Xavier and Hattersley, Andrew T and Melbye, Mads and Bisgaard, Hans and Pennell, Craig E and Widen, Elisabeth and Hakonarson, Hakon and Smith, George Davey and Heinrich, Joachim and Jarvelin, Marjo-Riitta and Jaddoe, Vincent W V and Early Genetics & Lifecourse Epidemiology (EAGLE) Consortium and Early Growth Genetics (EGG) Consortium and The Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium
Nature genetics, ISSN 1061-4036, 05/2013, Volume 45, Issue 6, pp. 713 - 713
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