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1. Full Text Abstract 15371: Prevalence and Electronic Health Record-Based Phenotype of Loss-Of-Function Genetic Variants in Arrhythmogenic Cardiomyopathy-Associated Genes in 61,000 Individuals
by Haggerty, Christopher M and Young, Wilson and James, Cynthia A and Calkins, Hugh and Jing, Linyuan and Hartzel, Dustin N and Leader, Joseph B and Fornwalt, Brandon K
Circulation, ISSN 0009-7322, 11/2018, Volume 138, Issue Suppl_1 Suppl 1, pp. A15371 - A15371
IntroductionArrhythmogenic cardiomyopathy (ACM) is associated with genetic variants in desmosome genes. Incidental findings of pathogenic/likely pathogenic... 
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2. Full Text First Trimester Plasma Glucose Values in Non-Diabetic Women are Associated with Risk for Congenital Heart Disease in Offspring
by Helle, Emmi I.T and Biegley, Preston and Knowles, Joshua W and Leader, Joseph B and Pendergrass, Sarah and Yang, Wei and Reaven, Gerald R and Shaw, Gary M and Ritchie, Marylyn and Priest, James R
The Journal of pediatrics, ISSN 0022-3476, 4/2018, Volume 195, pp. 275 - 278
plasma glucose | oral glucose tolerance test | congenital malformation | congenital heart disease | diabetes
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3. Full Text First trimester elevated serum glucose values are associated with congenital heart disease in the offspring
by Helle, Emmi and Yang, Wei and Knowles, Joshua W and Leader, Joseph B and Pendergrass, Sarah A and Ritchie, Marylyn D and Priest, James R and Reaven, Gary and Biegley, Preston S and Shaw, Gary M
Circulation, ISSN 0009-7322, 11/2016, Volume 134, Issue 19
Pregnancy | Complications and side effects | Congenital heart disease | Diabetes | Glucose | Health aspects | Risk factors | Dextrose
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4. Full Text Abstract 17229: First Trimester Elevated Serum Glucose Values Are Associated With Congenital Heart Disease in the Offspring
by Helle, Emmi and Biegley, Preston S and Knowles, Joshua W and Leader, Joseph B and Pendergrass, Sarah A and Reaven, Gary and Ritchie, Marylyn D and Shaw, Gary M and Yang, Wei and Priest, James R
Circulation, ISSN 0009-7322, 11/2016, Volume 134, Issue Suppl_1 Suppl 1, pp. A17229 - A17229
IntroductionMaternal diabetes mellitus (DM) during pregnancy is a well known and prevalent risk factor for congenital heart disease (CHD) in offspring. In... 
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5. Full Text Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease
by Dewey, Frederick E and Gusarova, Viktoria and Dunbar, Richard L and O’Dushlaine, Colm and Schurmann, Claudia and Gottesman, Omri and McCarthy, Shane and Van Hout, Cristopher V and Bruse, Shannon and Dansky, Hayes M and Leader, Joseph B and Murray, Michael F and Ritchie, Marylyn D and Kirchner, H. Lester and Habegger, Lukas and Lopez, Alex and Penn, John and Zhao, An and Shao, Weiping and Stahl, Neil and Murphy, Andrew J and Hamon, Sara and Bouzelmat, Aurelie and Zhang, Rick and Shumel, Brad and Pordy, Robert and Gipe, Daniel and Herman, Gary A and Sheu, Wayne H.H and Lee, I-Te and Liang, Kae-Woei and Guo, Xiuqing and Rotter, Jerome I and Chen, Yii-Der I and Kraus, William E and Shah, Svati H and Damrauer, Scott and Small, Aeron and Rader, Daniel J and Wulff, Anders Berg and Nordestgaard, Børge G and Tybjærg-Hansen, Anne and van den Hoek, Anita M and Princen, Hans M.G and Ledbetter, David H and Carey, David J and Overton, John D and Reid, Jeffrey G and Sasiela, William J and Banerjee, Poulabi and Shuldiner, Alan R and Borecki, Ingrid B and Teslovich, Tanya M and Yancopoulos, George D and Mellis, Scott J and Gromada, Jesper and Baras, Aris
The New England Journal of Medicine, ISSN 0028-4793, 07/2017, Volume 377, Issue 3, pp. 211 - 221
Loss-of-function variants in ANGPTL3 were associated with lower plasma levels of lipids and lower rates of coronary disease. A monoclonal antibody against... 
MEDICINE, GENERAL & INTERNAL | HEART-DISEASE | REMNANT CHOLESTEROL | PLASMA-LIPIDS | IMMUNOGLOBULIN GENES | ATHEROSCLEROSIS | RISK | CORONARY-ARTERY-DISEASE | FAMILIAL COMBINED HYPOLIPIDEMIA | LIPOPROTEIN-LIPASE GENE | TRANSGENIC MICE | Cardiovascular Diseases - prevention & control | Humans | Middle Aged | Antibodies, Monoclonal - adverse effects | Male | Angiopoietins - antagonists & inhibitors | Dose-Response Relationship, Drug | Dyslipidemias - blood | Angiopoietin-like Proteins | Lipids - blood | Female | Disease Models, Animal | Dyslipidemias - drug therapy | Atherosclerosis - drug therapy | Double-Blind Method | Antibodies, Monoclonal - pharmacology | Coronary Artery Disease - metabolism | Mice, Inbred Strains | Atherosclerosis - metabolism | Animals | Antibodies, Monoclonal - administration & dosage | Coronary Artery Disease - genetics | Lipid Metabolism - drug effects | Aged | Mice | Mutation | Angiopoietins - genetics | Cholesterol, LDL | Research | Antibiosis | Atherosclerosis | Lipoproteins (low density) | Medical research | Angiopoietin | Genomics | Genes | Coronary artery | Triglycerides | Biochemistry | Gene expression | Cholesterol | Serum levels | Proteins | Antagonism | Arteriosclerosis | Plasma levels | Cardiovascular diseases | Lipoproteins (high density) | Heart diseases | Drug dosages | Pharmaceuticals | Index Medicus | Abridged Index Medicus
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6. Full Text Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study
by Dewey, Frederick E and Murray, Michael F and Overton, John D and Habegger, Lukas and Leader, Joseph B and Fetterolf, Samantha N and O'Dushlaine, Colm and Van Hout, Cristopher V and Staples, Jeffrey and Gonzaga-Jauregui, Claudia and Metpally, Raghu and Pendergrass, Sarah A and Giovanni, Monica A and Kirchner, H. Lester and Balasubramanian, Suganthi and Abul-Husn, Noura S and Hartzel, Dustin N and Lavage, Daniel R and Kost, Korey A and Packer, Jonathan S and Lopez, Alexander E and Penn, John and Mukherjee, Semanti and Gosalia, Nehal and Kanagaraj, Manoj and Li, Alexander H and Mitnaul, Lyndon J and Adams, Lance J and Person, Thomas N and Praveen, Kavita and Marcketta, Anthony and Lebo, Matthew S and Austin-Tse, Christina A and Mason-Suares, Heather M and Bruse, Shannon and Mellis, Scott and Phillips, Robert and Stahl, Neil and Murphy, Andrew and Economides, Aris and Skelding, Kimberly A and Still, Christopher D and Elmore, James R and Borecki, Ingrid B and Yancopoulos, George D and Davis, F. Daniel and Faucett, William A and Gottesman, Omri and Ritchie, Marylyn D and Shuldiner, Alan R and Reid, Jeffrey G and Ledbetter, David H and Baras, Aris and Carey, David J
Science, ISSN 0036-8075, 12/2016, Volume 354, Issue 6319, pp. aaf6814 - aaf6814
The DiscovEHR collaboration between the Regeneron Genetics Center and Geisinger Health System couples high-throughput sequencing to an integrated health care... 
HEART-DISEASE | IDENTIFIES RARE | OF-FUNCTION VARIANTS | LOW-FREQUENCY | MULTIDISCIPLINARY SCIENCES | DENSITY-LIPOPROTEIN | B SYNTHESIS INHIBITOR | RISK | PCSK9 | ASSOCIATION | GENOME | Disease - genetics | Delivery of Health Care, Integrated | Gene Frequency | Genomics | Humans | Hypolipidemic Agents - pharmacology | Molecular Targeted Therapy | Sequence Analysis, DNA | INDEL Mutation | Exome - genetics | Lipids - blood | Drug Design | Adult | High-Throughput Nucleotide Sequencing | Polymorphism, Single Nucleotide | Electronic Health Records | Precision medicine | Genetic diversity | Index Medicus | Medicine | Health | Genes | Genetics | Lipids | Electronic health records | Patients | Blood
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7. Full Text Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease
by Dewey, Frederick E and Gusarova, Viktoria and O’Dushlaine, Colm and Gottesman, Omri and Trejos, Jesus and Hunt, Charleen and Van Hout, Cristopher V and Habegger, Lukas and Buckler, David and Lai, Ka-Man V and Leader, Joseph B and Murray, Michael F and Ritchie, Marylyn D and Kirchner, H. Lester and Ledbetter, David H and Penn, John and Lopez, Alexander and Borecki, Ingrid B and Overton, John D and Reid, Jeffrey G and Carey, David J and Murphy, Andrew J and Yancopoulos, George D and Baras, Aris and Gromada, Jesper and Shuldiner, Alan R
The New England Journal of Medicine, ISSN 0028-4793, 03/2016, Volume 374, Issue 12, pp. 1123 - 1133
This study showed an association of loss-of-function mutations in ANGPTL4 with low triglyceride levels and protection against coronary artery disease.... 
MEDICINE, GENERAL & INTERNAL | HEART-DISEASE | GENE | CHOLESTEROL | TRIGLYCERIDES | MICE | ANGIOPOIETIN-LIKE PROTEIN-4 | MUTATIONS | LIPOPROTEIN-LIPASE | PARTICIPANTS | LIPIDS | Cholesterol - blood | Humans | Middle Aged | Risk Factors | Gene Silencing | Male | Angiopoietins - antagonists & inhibitors | Macaca mulatta | Angiopoietin-like 4 Protein | Animals | Coronary Artery Disease - genetics | Triglycerides - blood | Female | Heterozygote | Aged | Mice | Mutation | Angiopoietins - genetics | Disease Models, Animal | Care and treatment | Triglycerides | Dosage and administration | Research | Coronary heart disease | Risk factors | Antilipemic agents | Enzymes | Angiopoietin | Exons | Genes | Coronary artery | Heterozygotes | Cardiovascular disease | Lipoprotein lipase | Lipase | Cholesterol | Homozygotes | Ischemia | Monoclonal antibodies | Cardiovascular diseases | Lipoproteins (high density) | Heart diseases | Index Medicus | Abridged Index Medicus
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8. Full Text Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes
by Gusarova, Viktoria and O'Dushlaine, Colm and Teslovich, Tanya M and Benotti, Peter N and Mirshahi, Tooraj and Gottesman, Omri and Van Hout, Cristopher V and Murray, Michael F and Mahajan, Anubha and Nielsen, Jonas B and Fritsche, Lars and Wulff, Anders Berg and Gudbjartsson, Daniel F and Sjögren, Marketa and Emdin, Connor A and Scott, Robert A and Lee, Wen-Jane and Small, Aeron and Kwee, Lydia C and Dwivedi, Om Prakash and Prasad, Rashmi B and Bruse, Shannon and Lopez, Alexander E and Penn, John and Marcketta, Anthony and Leader, Joseph B and Still, Christopher D and Kirchner, H. Lester and Mirshahi, Uyenlinh L and Wardeh, Amr H and Hartle, Cassandra M and Habegger, Lukas and Fetterolf, Samantha N and Tusie-Luna, Teresa and Morris, Andrew P and Holm, Hilma and Steinthorsdottir, Valgerdur and Sulem, Patrick and Thorsteinsdottir, Unnur and Rotter, Jerome I and Chuang, Lee-Ming and Damrauer, Scott and Birtwell, David and Brummett, Chad M and Khera, Amit V and Natarajan, Pradeep and Orho-Melander, Marju and Flannick, Jason and Lotta, Luca A and Willer, Cristen J and Holmen, Oddgeir L and Ritchie, Marylyn D and Ledbetter, David H and Murphy, Andrew J and Borecki, Ingrid B and Reid, Jeffrey G and Overton, John D and Hansson, Ola and Groop, Leif and Shah, Svati H and Kraus, William E and Rader, Daniel J and Chen, Yii-Der I and Hveem, Kristian and Wareham, Nicholas J and Kathiresan, Sekar and Melander, Olle and Stefansson, Kari and Nordestgaard, Børge G and Tybjærg-Hansen, Anne and Abecasis, Goncalo R and Altshuler, David and Florez, Jose C and Boehnke, Michael and McCarthy, Mark I and Yancopoulos, George D and Carey, David J and Shuldiner, Alan R and Baras, Aris and Dewey, Frederick E and Gromada, Jesper and Diabetes - Cardiovascular Disease and Kardiovaskulär forskning - hypertoni and Cardiovascular Research - Hypertension and Diabetes - kardiovaskulär sjukdom and Lund University and Genomics, Diabetes and Endocrinology and EpiHealth: Epidemiology for Health and Genomik, diabetes och endokrinologi and Institutionen för kliniska vetenskaper, Malmö and Lunds universitet and Department of Clinical Sciences, Malmö
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 2252 - 11
Angiopoietin-like 4 (ANGPTL4) is an endogenous inhibitor of lipoprotein lipase that modulates lipid levels, coronary atherosclerosis risk, and nutrient... 
HEART-DISEASE | REMNANT CHOLESTEROL | PLASMA-LIPIDS | MULTIDISCIPLINARY SCIENCES | MICE | ANGIOPOIETIN-LIKE PROTEIN-4 | LIPOPROTEIN-LIPASE | HAN CHINESE | CHINESE POPULATION | GENOME-WIDE ASSOCIATION | ADIPOSE-TISSUE | Diabetes Mellitus, Type 2 - genetics | Humans | Homeostasis | Male | Diabetes Mellitus, Type 2 - metabolism | Case-Control Studies | Genetic Variation | Diabetes Mellitus, Type 2 - etiology | Female | Lipoprotein Lipase - metabolism | Genetic Association Studies | Mice, Inbred C57BL | Risk Factors | Gene Silencing | Angiopoietin-like 4 Protein - deficiency | Mice, Knockout | Whole Exome Sequencing | Animals | Insulin Resistance - genetics | Angiopoietin-like 4 Protein - metabolism | Heterozygote | Mice | Blood Glucose - metabolism | Amino Acid Substitution | Angiopoietin-like 4 Protein - genetics | Deactivation | Angiopoietin | Diabetes mellitus | Health risks | Risk reduction | Risk | Lipoprotein lipase | Glucose | Lipase | Inactivation | Insulin | Proteins | Confidence intervals | Sensitivity | Nutrient loss | Rodents | Arteriosclerosis | Atherosclerosis | Genetics | Diabetes | Diabetes mellitus (non-insulin dependent) | Index Medicus | Medicinsk genetik | Basic Medicine | Medical Genetics | Clinical Medicine | Medical and Health Sciences | Endokrinologi och diabetes | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Klinisk medicin | Endocrinology and Diabetes
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9. Full Text Genetic identification of familial hypercholesterolemia within a single U.S. Health care system
by Abul-Husn, Noura S and Manickam, Kandamurugu and Jones, Laney K and Wright, Eric A and Hartzel, Dustin N and Gonzaga-Jauregui, Claudia and O'Dushlaine, Colm and Leader, Joseph B and Kirchner, H. Lester and Lindbuchler, D'Andra M and Barr, Marci L and Giovanni, Monica A and Ritchie, Marylyn D and Overton, John D and Reid, Jeffrey G and Metpally, Raghu P.R and Wardeh, Amr H and Borecki, Ingrid B and Yancopoulos, George D and Baras, Aris and Shuldiner, Alan R and Gottesman, Omri and Ledbetter, David H and Carey, David J and Dewey, Frederick E and Murray, Michael F
Science, ISSN 0036-8075, 12/2016, Volume 354, Issue 6319, pp. aaf7000 - aaf7000
Familial hypercholesterolemia (FH) remains underdiagnosed despite widespread cholesterol screening. Exome sequencing and electronic health record (EHR) data of... 
DIAGNOSIS | GENERAL-POPULATION | MANAGEMENT | CHOLESTEROL | VARIANTS | RECOMMENDATIONS | MULTIDISCIPLINARY SCIENCES | GUIDELINES | ASSOCIATION EXPERT PANEL | PREVALENCE | GENOME | United States - epidemiology | Genetic Testing | Prevalence | Humans | Hyperlipoproteinemia Type II - diagnosis | Exome - genetics | Coloring Agents - therapeutic use | Hyperlipoproteinemia Type II - epidemiology | Delivery of Health Care | Heterozygote | Coronary Artery Disease - epidemiology | Electronic Health Records | Drug Utilization - statistics & numerical data | Lipoproteins, LDL - blood | Hyperlipoproteinemia Type II - genetics | Lipids | Cardiovascular disease | Family medical history | Genomics | Risk factors | Index Medicus | Carriers | Screening | Health | Risk | Genetics | Diagnosis | Electronic health records | Patients
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10. Full Text Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease
by Khera, Amit V and Won, Hong-Hee and Peloso, Gina M and O’Dushlaine, Colm and Liu, Dajiang and Stitziel, Nathan O and Natarajan, Pradeep and Nomura, Akihiro and Emdin, Connor A and Gupta, Namrata and Borecki, Ingrid B and Asselta, Rosanna and Duga, Stefano and Merlini, Piera Angelica and Correa, Adolfo and Kessler, Thorsten and Wilson, James G and Bown, Matthew J and Hall, Alistair S and Braund, Peter S and Carey, David J and Murray, Michael F and Kirchner, H. Lester and Leader, Joseph B and Lavage, Daniel R and Manus, J. Neil and Hartzel, Dustin N and Samani, Nilesh J and Schunkert, Heribert and Marrugat, Jaume and Elosua, Roberto and McPherson, Ruth and Farrall, Martin and Watkins, Hugh and Lander, Eric S and Rader, Daniel J and Danesh, John and Ardissino, Diego and Gabriel, Stacey and Willer, Cristen and Abecasis, Gonçalo R and Saleheen, Danish and Dewey, Frederick E and Kathiresan, Sekar and Global Lipids Genetics Consortium and DiscovEHR Study Grp and Myocardial Infarction Genetics and CARDIoGRAM Exome Consortium and Myocardial Infarction Genetics Consortium, DiscovEHR Study Group, CARDIoGRAM Exome Consortium, and Global Lipids Genetics Consortium and for the Myocardial Infarction Genetics Consortium, DiscovEHR Study Group, CARDIoGRAM Exome Consortium, and Global Lipids Genetics Consortium
JAMA, ISSN 0098-7484, 03/2017, Volume 317, Issue 9, pp. 937 - 946
IMPORTANCE: The activity of lipoprotein lipase (LPL) is the rate-determining step in clearing triglyceride-rich lipoproteins from the circulation. Mutations... 
POPULATION | MEDICINE, GENERAL & INTERNAL | HEART-DISEASE | MYOCARDIAL-INFARCTION | VARIANTS | CHOLESTEROL | NONFASTING TRIGLYCERIDES | RISK | OF-FUNCTION MUTATIONS | MENDELIAN RANDOMIZATION | DEFICIENCY | Cross-Sectional Studies | Lipoprotein Lipase - genetics | Humans | Middle Aged | Genotype | Male | Lipoproteins - blood | Case-Control Studies | Age of Onset | Coronary Artery Disease - genetics | Triglycerides - blood | Adult | Female | Heterozygote | Mutation | Odds Ratio | Lipoprotein lipase | Research | Gene mutations | Coronary heart disease | Genotype & phenotype | Cardiovascular disease | Lipoproteins | Risk factors | Index Medicus | Abridged Index Medicus
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11. Full Text 238-LB: Prevalence of GCK-MODY in 92,412 Exomes from an Unselected Clinical Population
by MIRSHAHI, UYENLINH L and GOEHRINGER, JESSICA M and HU, YING and WARDEH, AMR H and WILLIAMS, JANET and MANNEY, CATARINA B and STAPLES, JEFFREY C and LEADER, JOSEPH B and SHULDINER, ALAN R and POLLIN, TONI I and CAREY, DAVID J
Diabetes, ISSN 0012-1797, 06/2019, Volume 68, Issue Supplement 1, p. 238
Maturity onset diabetes of the young (MODY) is a monogenic form of diabetes attributed to a highly penetrant variant in one of several genes, including GCK.... 
Hyperglycemia | Phenotypes | Fasting | Gene frequency | Diabetes mellitus | Fetuses | Glucose | Diabetes | Diabetes mellitus (non-insulin dependent)
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12. Full Text Contrasting Association Results between Existing PheWAS Phenotype Definition Methods and Five Validated Electronic Phenotypes
by Leader, Joseph B and Pendergrass, Sarah A and Verma, Anurag and Carey, David J and Hartzel, Dustin N and Ritchie, Marylyn D and Kirchner, H Lester
AMIA ... Annual Symposium proceedings. AMIA Symposium, 2015, Volume 2015, pp. 824 - 832
Phenome-Wide Association Studies (PheWAS) comprehensively investigate the association between genetic variation and a wide array of outcome traits. Electronic... 
Genetic Variation | International Classification of Diseases | Genome-Wide Association Study | Phenotype | Algorithms | Humans | Polymorphism, Single Nucleotide | Electronic Health Records | Index Medicus
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13. Full Text Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease
by Nomura, Akihiro and Won, Hong-Hee and Khera, Amit V and Takeuchi, Fumihiko and Ito, Kaoru and McCarthy, Shane and Emdin, Connor A and Klarin, Derek and Natarajan, Pradeep and Zekavat, Seyedeh M and Gupta, Namrata and Peloso, Gina M and Borecki, Ingrid B and Teslovich, Tanya M and Asselta, Rosanna and Duga, Stefano and Merlini, Piera A and Correa, Adolfo and Kessler, Thorsten and Wilson, James G and Bown, Matthew J and Hall, Alistair S and Braund, Peter S and Carey, David J and Murray, Michael F and Kirchner, H. Lester and Leader, Joseph B and Lavage, Daniel R and Manus, J. Neil and Hartze, Dustin N and Samani, Nilesh J and Schunkert, Heribert and Marrugat, Jaume and Elosua, Roberto and McPherson, Ruth and Farrall, Martin and Watkins, Hugh and Juang, Jyh-Ming J and Hsiung, Chao A and Lin, Shih-Yi and Wang, Jun-Sing and Tada, Hayato and Kawashiri, Masa-Aki and Inazu, Akihiro and Yamagishi, Masakazu and Katsuya, Tomohiro and Nakashima, Eitaro and Nakatochi, Masahiro and Yamamoto, Ken and Yokota, Mitsuhiro and Momozawa, Yukihide and Rotter, Jerome I and Lander, Eric S and Rader, Daniel J and Danesh, John and Ardissino, Diego and Gabriel, Stacey and Willer, Cristen J and Abecasis, Goncalo R and Saleheen, Danish and Kubo, Michiaki and Kato, Norihiro and Ida Chen, Yii-Der and Dewey, Frederick E and Kathiresan, Sekar and DiscovEHR Study Grp and Taichi Consortium
Circulation Research, ISSN 0009-7330, 06/2017, Volume 121, Issue 1, pp. 81 - 88
Rationale: Therapies that inhibit CETP (cholesteryl ester transfer protein) have failed to demonstrate a reduction in risk for coronary heart disease (CHD).... 
coronary disease | lipids | cholesteryl ester transfer protein | case-control studies | CETP | CARDIAC & CARDIOVASCULAR SYSTEMS | PROTECTION | POLYMORPHISM | DEFICIENCY | HDL | DENSITY-LIPOPROTEIN CHOLESTEROL | INHIBITION | METABOLISM | PERIPHERAL VASCULAR DISEASE | MUTATIONS | HEMATOLOGY | ASSOCIATION | Coronary Disease - blood | Humans | Middle Aged | Risk Factors | Male | Coronary Disease - diagnosis | Case-Control Studies | Cholesterol Ester Transfer Proteins - blood | Coronary Disease - genetics | Cholesterol Ester Transfer Proteins - genetics | Adult | Female | Aged | Genetic Variation - genetics | Nucleotide sequence | Exons | Lipids | Cardiovascular disease | Triglycerides | CETP gene | Low density lipoprotein | Coronary artery disease | Cholesterol | Cholesteryl ester transfer protein | Confidence intervals | Proteins | Health risk assessment | Heart diseases | Index Medicus | Lipids and Cholesterol | exome sequencing | genetics | coronary heart disease | protein truncating variants | Coronary Artery Disease | human
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14. Full Text The limited utility of the double-blind food challenge in diagnosing non-IgE mediated cow’s milk allergy in infants
by Wallace, Kathleen G and Virkud, Yamini V and Patil, Sarita U and Leader, Joseph B and Southwick, Caroline and Katz, Aubrey J and Shreffler, Wayne G and Virk Hundal, Navneet K
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 02/2018, Volume 141, Issue 2, pp. AB256 - AB256
Infants received 90ml of active (1.6g cow’s milk protein (CMP) + amino acid formula (AAF)) or placebo (AAF) formula daily for one week. High-threshold CMA... 
Immunoglobulin E | Food allergies | Infants | Cow's milk | Medical diagnosis | Food hypersensitivity
Journal Article
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