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1. Full Text Abstract 37: Secondary Stroke Prevention With Aspirin and Clopidogrel in CYP2C19 17 Carriers Increases Risk of Major Non-CNS Bleeding
by Simpkins, Alexis N and McDonough, Caitrin W and McClure, Leslie A and Mitchell, Braxton D and Shuldiner, Alan R and Benavente, Oscar R and Johnson, Julie A
Stroke, ISSN 0039-2499, 02/2019, Volume 50, Issue Suppl_1
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2. Full Text Pharmacogenetic Associations of Ī²1-Adrenergic Receptor Polymorphisms With Cardiovascular Outcomes in the SPS3 Trial (Secondary Prevention of Small Subcortical Strokes)
by Magvanjav, Oyunbileg and McDonough, Caitrin W and Gong, Yan and McClure, Leslie A and Talbert, Robert L and Horenstein, Richard B and Shuldiner, Alan R and Benavente, Oscar R and Mitchell, Braxton D and Johnson, Julie A and NINDS SiGN (Stroke Genetics Network)
Stroke, ISSN 0039-2499, 03/2017, Volume 48, Issue 5, pp. 1337 - 1343
BACKGROUND AND PURPOSEā€”Functional polymorphisms (Ser49Gly and Arg389Gly) in ADRB1 have been associated with cardiovascular and Ī²-blocker response outcomes.... 
Ser49Gly | cardiovascular disease | ADRB1 | Ī²-blockers | stroke | pharmacogenetics | Myocardial Infarction - chemically induced | Myocardial Infarction - genetics | Pharmacogenetics | Stroke - prevention & control | Follow-Up Studies | Humans | Middle Aged | Brain Ischemia - genetics | Male | Brain Ischemia - prevention & control | Secondary Prevention | Stroke - genetics | Polymorphism, Genetic | Stroke - chemically induced | Adrenergic beta-Antagonists - adverse effects | Female | Receptors, Adrenergic, beta-1 - genetics | Aged | Myocardial Infarction - prevention & control | Brain Ischemia - chemically induced | beta-blockers
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3. Full Text Plasma Renin Activity Is a Predictive Biomarker of Blood Pressure Response in European but not in African Americans With Uncomplicated Hypertension
by Mehanna, Mai and Wang, Zhiying and Gong, Yan and McDonough, Caitrin W and Beitelshees, Amber L and Gums, John G and Chapman, Arlene B and Schwartz, Gary L and Bailey, Kent R and Johnson, Julie A and Turner, Stephen T and Cooper-DeHoff, Rhonda M
American journal of hypertension, ISSN 0895-7061, 06/2019, Volume 32, Issue 7, pp. 668 - 675
Interindividual variability in blood pressure (BP) response to antihypertensives has been reported. Although plasma renin activity (PRA) is a potential... 
African Americans | blood pressure | plasma renin activity | hypertension | European Americans
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4. Full Text Pharmacogenomics of osteonecrosis of the jaw
by Yang, Guang and Singh, Sonal and Chen, Yiqing and Hamadeh, Issam S and Langaee, Taimour and McDonough, Caitrin W and Holliday, L. Shannon and Lamba, Jatinder K and Moreb, Jan S and Katz, Joseph and Gong, Yan
Bone, ISSN 8756-3282, 07/2019, Volume 124, pp. 75 - 82
Osteonecrosis of the jaw (ONJ) is a rare but serious drug induced adverse event, mainly associated with the use of antiresorptive medications, such as... 
Genome-wide association study | Whole exome sequencing | Bisphosphonates | Osteonecrosis of the jaw | Pharmacogenomics | Osteoporosis | Genetic markers | Pharmacogenetics | Anopheles | Analysis | Phosphonates | Cytochrome P-450 | Bones | Density
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5. Full Text Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study
by Pulit, Sara L and McArdle, Patrick F and Wong, Quenna and Malik, Rainer and Gwinn, Katrina and Achterberg, Sefanja and Algra, Ale and Amouyel, Philippe and Anderson, Christopher D and Arnett, Donna K Arnett and Arnett, Donna K and Arsava, Ethem Murat and Attia, John and Ay, Hakan and Bartz, Traci M and Battey, Thomas and Benavente, Oscar and Benavente, Oscar R and Bevan, Steve and Biffi, Alessandro and Bis, Joshua C and Blanton, Susan H and Boncoraglio, Giorgio B and Brown, Robert D and Burgess, Annette I and Carrera, Caty and Chapman Smith, Sherita N and Chasman, Daniel I and Chauhan, Ganesh and Chen, Wei-Min and Cheng, Yu-Ching and Chong, Michael and Cloonan, Lisa K and Cole, John W and Cotlarciuc, Ioana and Cruchaga, Carlos and Cuadrado-Godia, Elisa and Dave, Tushar and Dawson, Jesse and Debette, StƩphanie and Delavaran, Hossein and Dell, Cameron A and Dichgans, Martin and Doheny, Kimberly F and Dong, Chuanhui and Duggan, David J and Engstrƶm, Gunnar and Evans, Michele K and PallejƠ, Xavier Estivill and Faul, Jessica D and FernƔndez-Cadenas, Israel and Fornage, Myriam and Frossard, Philippe M and Furie, Karen and Gamble, Dale M and Gieger, Christian and Giese, Anne-Katrin and Giralt-Steinhauer, Eva and GonzƔlez, Hector M and Goris, An and Gretarsdottir, Solveig and Grewal, Raji P and Grittner, Ulrike and Gustafsson, Stefan and Han, Buhm and Hankey, Graeme J and Heitsch, Laura and Higgins, Peter and Hochberg, Marc C and Holliday, Elizabeth and Hopewell, Jemma C and Horenstein, Richard B and Howard, George and Ikram, M Arfan and Ilinca, Andreea and Ingelsson, Erik and Irvin, Marguerite R and Jackson, Rebecca D and Jern, Christina and Conde, Jordi JimƩnez and Johnson, Julie A and Jood, Katarina and Kahn, Muhammad S and Kaplan, Robert and Kappelle, L Jaap and Kardia, Sharon L R and Keene, Keith L and Kissela, Brett M and Kleindorfer, Dawn O and Koblar, Simon and Labovitz, Daniel and Launer, Lenore J and Laurie, Cathy C and Laurie, Cecelia A and Lee, Jin-Moo and Lee, Cue Hyunkyu and Lehm, Manuel and Lemmens, Robin and Levi, Christopher and Leys, Didier and ... and NINDS Stroke Genetics Network SiGN and ISGC and International Stroke Genetics Consortium (ISGC) and NINDS Stroke Genetics Network (SiGN) and Institutionen fƶr neurovetenskap och fysiologi, sektionen fƶr klinisk neurovetenskap och rehabilitering and Institute of Neuroscience and Physiology and Institutionen fƶr biomedicin, avdelningen fƶr medicinsk genetik och klinisk genetik and Gƶteborgs universitet and Gothenburg University and Institute of Biomedicine, Department of Pathology and Institute of Biomedicine, Department of Medical and Clinical Genetics and Sahlgrenska Academy and Institute of Neuroscience and Physiology, Department of Clinical Neuroscience and Rehabilitation and Institutionen fƶr biomedicin, avdelningen fƶr patologi and Sahlgrenska akademin and Institutionen fƶr neurovetenskap och fysiologi
Lancet Neurology, The, ISSN 1474-4422, 2016, Volume 15, Issue 2, pp. 174 - 184
Summary Background The discovery of disease-associated loci through genome-wide association studies (GWAS) is the leading genetic approach to the... 
Neurology | COMMON VARIANTS | IMPUTATION | METAANALYSIS | REPLICATION | TOAST | CAUSATIVE CLASSIFICATION | RISK | CLINICAL NEUROLOGY | ATRIAL-FIBRILLATION | Brain Ischemia - classification | Humans | Middle Aged | Brain Ischemia - genetics | Genetic Loci | Nerve Tissue Proteins - genetics | Case-Control Studies | Stroke - genetics | Young Adult | Stroke - classification | Adolescent | Aged, 80 and over | Adult | Aged | Genome-Wide Association Study - methods | Tetraspanins - genetics | Cohort Studies | Ischemia | Genetic research | Genomics | Disease susceptibility | Studies | Stroke | Genealogy | Medical imaging | Classification | Atherosclerosis | Genomes | Methods | Veins & arteries | Medicinska grundvetenskaper | Basic Medicine
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6. Full Text Multisite Investigation of Outcomes WithĀ Implementation of CYP2C19 Genotype-Guided Antiplatelet Therapy After Percutaneous Coronary Intervention
by Cavallari, Larisa H and Lee, Yee Ming and Lee, Craig R and Beitelshees, Amber L and Cooper-DeHoff, Rhonda M and Duarte, Julio D and Voora, Deepak and Kimmel, Stephen E and McDonough, Caitrin W and Gong, Yan and Dave, Chintan V and Pratt, Victoria M and Alestock, Tameka D and Anderson, R. David and Alsip, Jorge and Ardati, Amer K and Brott, Brigitta C and Brown, Lawrence and Chumnumwat, Supatat and Clare-Salzler, Michael J and Coons, James C and Denny, Joshua C and Dillon, Chrisly and Elsey, Amanda R and Hamadeh, Issam S and Harada, Shuko and Hillegass, William B and Hines, Lindsay and Horenstein, Richard B and Howell, Lucius A and Jeng, Linda J.B and Kelemen, Mark D and Magvanjav, Oyunbileg and Montasser, May and Nelson, David R and Nutescu, Edith A and Nwaba, Devon C and Pakyz, Ruth E and Palmer, Kathleen and Peterson, Josh F and Pollin, Toni I and Quinn, Alison H and Robinson, Shawn W and Schub, Jamie and Skaar, Todd C and Smith, D. Max and Sriramoju, Vindhya B and Starostik, Petr and Stys, Tomasz P and Stevenson, James M and Varunok, Nicholas and Vesely, Mark R and Wake, Dyson T and Weck, Karen E and Weitzel, Kristin W and Wilke, Russell A and Willig, James and Zhao, Richard Y and Kreutz, Rolf P and Stouffer, George A and Empey, Philip E and Limdi, Nita A and Shuldiner, Alan R and Winterstein, Almut G and Johnson, Julie A and IGNITE Network
JACC: Cardiovascular Interventions, ISSN 1936-8798, 01/2018, Volume 11, Issue 2, pp. 181 - 191
This multicenter pragmatic investigation assessed outcomes following clinical implementation of genotypeā€“guided antiplatelet therapy after percutaneous... 
cardiovascular events | clopidogrel | percutaneous coronary intervention | pharmacogenomics | antiplatelet therapy | CYP2C19 | CARDIAC & CARDIOVASCULAR SYSTEMS | METAANALYSIS | CLOPIDOGREL THERAPY | POLYMORPHISMS | TASK-FORCE | HEART-ASSOCIATION | PHARMACOGENETICS | PRASUGREL | ARTERY-DISEASE | CLINICAL-OUTCOMES | PRAGMATIC TRIALS | Predictive Value of Tests | Percutaneous Coronary Intervention - mortality | United States | Humans | Middle Aged | Male | Patient Selection | Ticagrelor - adverse effects | Time Factors | Clinical Decision-Making | Pharmacogenomic Variants | Female | Platelet Aggregation Inhibitors - therapeutic use | Ticagrelor - therapeutic use | Platelet Aggregation Inhibitors - adverse effects | Pharmacogenetics | Risk Assessment | Risk Factors | Cytochrome P-450 CYP2C19 - genetics | Treatment Outcome | Prasugrel Hydrochloride - adverse effects | Pharmacogenomic Testing | Prasugrel Hydrochloride - therapeutic use | Drug Resistance - genetics | Aged | Clopidogrel - adverse effects | Clopidogrel - therapeutic use | Percutaneous Coronary Intervention - adverse effects
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7. Full Text Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci
by Tragante, Vinicius and Barnes, MichaelĀ R and Ganesh, SanthiĀ K and Lanktree, MatthewĀ B and Guo, Xiuqing and Guo, Wei and Franceschini, Nora and Smith, ErinĀ N and Johnson, AndrewĀ D and Johnson, JulieĀ A and Johnson, Toby and Holmes, MichaelĀ V and Padmanabhan, Sandosh and Karczewski, KonradĀ J and Almoguera, Berta and Barnard, John and Baumert, Jens and Chang, Yen-PeiĀ Christy and Elbers, ClaraĀ C and Farrall, Martin and Fischer, MaryĀ E and Gaunt, TomĀ R and Gho, JohannesĀ M.I.H and Gieger, Christian and Goel, Anuj and Gong, Yan and Isaacs, Aaron and Kleber, MarcusĀ E and Leach, IreneĀ Mateo and McDonough, CaitrinĀ W and Meijs, MatthijsĀ F.L and Melander, Olle and Nelson, ChristopherĀ P and Nolte, IljaĀ M and Pankratz, Nathan and Price, TomĀ S and Shaffer, Jonathan and Shah, Sonia and Tomaszewski, Maciej and vanĀ derĀ Most, PeterĀ J and VanĀ Iperen, ErikĀ P.A and Vonk, JudithĀ M and Witkowska, Kate and Wong, CarolineĀ O.L and Zhang, Li and Beitelshees, AmberĀ L and Berenson, GeraldĀ S and Bhatt, DeepakĀ L and Brown, Morris and Burt, Amber and Cooper-DeHoff, RhondaĀ M and Connell, JohnĀ M and Cruickshanks, KarenĀ J and Curtis, SeanĀ P and Davey-Smith, George and Delles, Christian and Gansevoort, RonĀ T and Haiqing, Shen and Hastie, ClaireĀ E and Hofker, MartenĀ H and Hovingh, G.Ā Kees and Kim, DanielĀ S and Kirkland, SusanĀ A and Klein, BarbaraĀ E and Klein, Ronald and Li, YunĀ R and Maiwald, Steffi and Newton-Cheh, Christopher and Oā€™Brien, EoinĀ T and Onland-Moret, N.Ā Charlotte and Palmas, Walter and Parsa, Afshin and Penninx, BrendaĀ W and Pettinger, Mary and Vasan, Ramachandran S and Ranchalis, JaneĀ E and M Ridker, Paul and Rose, LyndaĀ M and Sever, Peter and Shimbo, Daichi and Steele, Laura and Stolk, RonaldĀ P and Thorand, Barbara and Trip, MiekeĀ D and vanĀ Duijn, CorneliaĀ M and Verschuren, W.Ā Monique and Wijmenga, Cisca and Wyatt, Sharon and Young, J.Ā Hunter and Zwinderman, AeilkoĀ H and Bezzina, ConnieĀ R and Boerwinkle, Eric and Casas, JuanĀ P and Caulfield, MarkĀ J and Chakravarti, Aravinda and Chasman, DanielĀ I and Davidson, KarinaĀ W and Doevendans, PieterĀ A and Dominiczak, AnnaĀ F and FitzGerald, GarretĀ A and ... and KardiovaskulƤr forskning - hypertoni and Cardiovascular Research - Hypertension and EpiHealth: Epidemiology for Health and Lund University and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
The American Journal of Human Genetics, ISSN 0002-9297, 03/2014, Volume 94, Issue 3, pp. 349 - 360
Blood pressure (BP) is a heritable risk factor for cardiovascular disease. To investigate genetic associations with systolic BP (SBP), diastolic BP (DBP), mean... 
COMMON VARIANTS | CANDIDATE GENES | DRUG DISCOVERY | GENETICS & HEREDITY | HUMAN PREFRONTAL CORTEX | FACTOR-KAPPA-B | ESSENTIAL-HYPERTENSION | SUSCEPTIBILITY LOCUS | PULSE PRESSURE | CORONARY-ARTERY-DISEASE | GENOME-WIDE ASSOCIATION | Blood Pressure | Genetics, Population | Computational Biology - methods | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Diastole | Europe | Humans | Risk Factors | Genotype | Genetic Loci | Systole | Phenotype | Arterial Pressure | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Quality Control | Quantitative trait loci | Physiological aspects | Genetic research | Blood pressure | Genetic aspects | Research | Identification and classification | Meta-analysis | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hƤlsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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8. Full Text Hypertension in Florida: Data from the one Florida clinical data research network
by Smith, Steven M and McAuliffe, Kathryn and Hall, Jaclyn M and McDonough, Caitrin W and Gurka, Matthew J and Robinson, Temple O and Sacco, Ralph L and Pepine, Carl and Shenkman, Elizabeth and Cooper-DeHoff, Rhonda M
Preventing Chronic Disease, ISSN 1545-1151, 03/2018, Volume 15, Issue 3
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9. Full Text Genomic Association Analysis of Common Variants Influencing Antihypertensive Response to Hydrochlorothiazide
by Turner, Stephen T and Boerwinkle, Eric and Oā€™Connell, Jeffrey R and Bailey, Kent R and Gong, Yan and Chapman, Arlene B and McDonough, Caitrin W and Beitelshees, Amber L and Schwartz, Gary L and Gums, John G and Padmanabhan, Sandosh and Hiltunen, Timo P and Citterio, Lorena and Donner, Kati M and Hedner, Thomas and Lanzani, Chiara and Melander, Olle and Saarela, Janna and Ripatti, Samuli and Wahlstrand, Bjƶrn and Manunta, Paolo and Kontula, Kimmo and Dominiczak, Anna F and Cooper-DeHoff, Rhonda M and Johnson, Julie A and KardiovaskulƤr forskning - hypertoni and Cardiovascular Research - Hypertension and EpiHealth: Epidemiology for Health and Lund University and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
Hypertension, ISSN 0194-911X, 08/2013, Volume 62, Issue 2, pp. 391 - 397
To identify novel genes influencing blood pressure response to thiazide diuretic therapy for hypertension, we conducted genome-wide association meta-analyses... 
Hypertension | Protein kinase C | Hydrochlorothiazide | Genomics | Antihypertensive agents | Pharmacogenomics | GENOMEWIDE ASSOCIATION | antihypertensive agents | POLYMORPHISM | pharmacogenomics | PREDICTORS | hydrochlorothiazide | DRUGS | BLOOD-PRESSURE RESPONSE | genomics | PERIPHERAL VASCULAR DISEASE | ESSENTIAL-HYPERTENSION | hypertension | protein kinase C | BLOCKER | Genome-Wide Association Study | Humans | Middle Aged | Protein Kinase C-alpha - genetics | Hypertension - drug therapy | Male | Transcription Factors - genetics | Antihypertensive Agents - therapeutic use | Atenolol - therapeutic use | Chromosomes, Human, Pair 17 | Adult | Diuretics - therapeutic use | Female | Blood Pressure - drug effects | Polymorphism, Single Nucleotide | Hypertension - genetics | Hydrochlorothiazide - therapeutic use | antihypertensive therapy | diuretics | high blood pressure | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Medical and Health Sciences | Medicin och hƤlsovetenskap | Klinisk medicin
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10. Full Text A genetic response score for hydrochlorothiazide use
by Shahin, Mohamed H and Gong, Yan and McDonough, Caitrin W and Rotroff, Daniel M and Beitelshees, Amber L and Garrett, Timothy J and Gums, John G and Motsinger-Reif, Alison and Chapman, Arlene B and Turner, Stephen T and Boerwinkle, Eric and Frye, Reginald F and Fiehn, Oliver and Cooper-Dehoff, Rhonda M and Kaddurah-Daouk, Rima and Johnson, Julie A
Hypertension, ISSN 0194-911X, 09/2016, Volume 68, Issue 3, pp. 621 - 629
metabolomics | hypertension | pharmacogenetics | genome-wide association study | hydrochlorothiazide
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11. Full Text Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci
by Asselbergs, FolkertĀ W and Guo, Yiran and vanĀ Iperen, ErikĀ P.A and Sivapalaratnam, Suthesh and Tragante, Vinicius and Lanktree, MatthewĀ B and Lange, LeslieĀ A and Almoguera, Berta and Appelman, YolandeĀ E and Barnard, John and Baumert, Jens and Beitelshees, AmberĀ L and Bhangale, TusharĀ R and Chen, Yii-DerĀ Ida and Chen, Wei and Gaunt, TomĀ R and Gong, Yan and Hopewell, JemmaĀ C and Johnson, Toby and Johnson, JulieĀ A and Kleber, MarcusĀ E and Langaee, TaimourĀ Y and Li, Mingyao and Li, YunĀ R and Liu, Kiang and McDonough, CaitrinĀ W and Meijs, MatthijsĀ F.L and Middelberg, RitaĀ P.S and Musunuru, Kiran and Nelson, ChristopherĀ P and Oā€™Connell, JefferyĀ R and Padmanabhan, Sandosh and Pankow, JamesĀ S and Pankratz, Nathan and Rafelt, Suzanne and Rajagopalan, Ramakrishnan and Romaine, SimonĀ P.R and Schork, NicholasĀ J and Shaffer, Jonathan and Shen, Haiqing and Smith, ErinĀ N and Tischfield, SamĀ E and vanĀ derĀ Most, PeterĀ J and vanĀ Vliet-Ostaptchouk, JanaĀ V and Verweij, Niek and Volcik, KellyĀ A and Zhang, Li and Bailey, KristianĀ M and Bailey, KentĀ R and Bauer, Florianne and Boer, JolandaĀ M.A and Braund, PeterĀ S and Burt, Amber and Burton, PaulĀ R and Buxbaum, SarahĀ G and Cooper-DeHoff, RhondaĀ M and Cupples, L.Ā Adrienne and deJong, JonasĀ S and Delles, Christian and Duggan, David and Fornage, Myriam and Furlong, ClementĀ E and Glazer, Nicole and Gums, JohnĀ G and Hastie, Claire and Holmes, MichaelĀ V and Illig, Thomas and Kirkland, SusanĀ A and Kivimaki, Mika and Klein, BarbaraĀ E and Klein, Ronald and Kooperberg, Charles and Kottke-Marchant, Kandice and Kumari, Meena and LaCroix, AndreaĀ Z and Mallela, Laya and Murugesan, Gurunathan and Ordovas, Jose and Ouwehand, WillemĀ H and Post, WendyĀ S and Saxena, Richa and Scharnagl, Hubert and Schreiner, PamelaĀ J and Shah, Tina and Shields, DenisĀ C and Shimbo, Daichi and Srinivasan, SathanurĀ R and Stolk, RonaldĀ P and Swerdlow, DanielĀ I and Taylor, HermanĀ A and Topol, EricĀ J and Toskala, Elina and vanĀ Pelt, JoostĀ L and vanĀ Setten, Jessica and Yusuf, Salim and Whittaker, JohnĀ C and Zwinderman, A.H and Anand, SoniaĀ S and Balmforth, AnthonyĀ J and Berenson, GeraldĀ S and ... and LifeLines Cohort Study and KardiovaskulƤr forskning - hypertoni and Cardiovascular Research - Hypertension and EpiHealth: Epidemiology for Health and Lund University and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
The American Journal of Human Genetics, ISSN 0002-9297, 11/2012, Volume 91, Issue 5, pp. 823 - 838
Genome-wide association studies (GWASs) have identified many SNPs underlying variations in plasma-lipid levels. We explore whether additional loci associated... 
DENSITY-LIPOPROTEIN CHOLESTEROL | FAMILIAL HYPERCHOLESTEROLEMIA | QUANTITATIVE TRAITS | APOLIPOPROTEIN B-100 | GENETICS & HEREDITY | MISSING HERITABILITY | CORONARY-HEART-DISEASE | COMPLEX TRAITS | GENOME-WIDE ASSOCIATION | PLASMA TRIGLYCERIDES | STATISTICAL-MODEL | Genome-Wide Association Study | Lipids - genetics | Humans | European Continental Ancestry Group | Genotype | Male | Cholesterol, HDL - genetics | Cholesterol, LDL - genetics | Phenotype | Lipids - blood | Sex Factors | Triglycerides - blood | Cholesterol, HDL - blood | Cholesterol, LDL - blood | Female | Polymorphism, Single Nucleotide | Triglycerides - genetics | Quantitative Trait Loci | Europeans | Usage | Genome-wide association studies | Genetic variation | Cholesterol, HDL | Multifactorial traits | Genetic aspects | Research | Health aspects | Genetic screening | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hƤlsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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