Muin J. Khoury
#61,144
Most Influential Person Now
American geneticist and epidemiologist
Muin J. Khoury's AcademicInfluence.com Rankings
Muin J. Khourymedical Degrees
Medical
#665
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#888
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#243
USA Rank
Epidemiology
#115
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#126
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#29
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Muin J. Khourybiology Degrees
Biology
#3784
World Rank
#5738
Historical Rank
#1504
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Genetics
#299
World Rank
#352
Historical Rank
#135
USA Rank
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Medical Biology
Muin J. Khoury's Degrees
- Masters Public Health Johns Hopkins University
- PhD Epidemiology University of California, Berkeley
Why Is Muin J. Khoury Influential?
(Suggest an Edit or Addition)According to Wikipedia, Muin Joseph Khoury is an American geneticist and epidemiologist who conducts research in the field of public health genomics. He is the founding director of the Office of Public Health Genomics at the Centers for Disease Control and Prevention since 1997. He has also been a senior advisor in public health genomics at the National Cancer Institute since 2007.
Muin J. Khoury's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Increasing value and reducing waste in research design, conduct, and analysis (2014) (1144)
- Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database (2008) (1064)
- The continuum of translation research in genomic medicine: how can we accelerate the appropriate integration of human genome discoveries into health care and disease prevention? (2007) (685)
- Neural-tube defects. (1999) (649)
- Diabetes mellitus during pregnancy and the risks for specific birth defects: a population-based case-control study. (1990) (612)
- National Institutes of Health approaches to dissemination and implementation science: current and future directions. (2012) (589)
- Assessment of cumulative evidence on genetic associations: interim guidelines. (2008) (559)
- Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database (2012) (546)
- Strengthening the reporting of genetic association studies (STREGA): an extension of the STROBE statement (2009) (494)
- STrengthening the REporting of Genetic Association Studies (STREGA)— An Extension of the STROBE Statement (2009) (482)
- Deploying whole genome sequencing in clinical practice and public health: Meeting the challenge one bin at a time (2011) (475)
- Fundamentals of Genetic Epidemiology (1993) (437)
- Nontraditional epidemiologic approaches in the analysis of gene-environment interaction: case-control studies with no controls! (1996) (430)
- Population-based study of congenital heart defects in Down syndrome. (1998) (416)
- Population screening in the age of genomic medicine. (2003) (405)
- A navigator for human genome epidemiology (2008) (400)
- Reporting, appraising, and integrating data on genotype prevalence and gene-disease associations. (2002) (395)
- Letting the genome out of the bottle--will we get our wish? (2008) (368)
- Sodium and potassium intake and mortality among US adults: prospective data from the Third National Health and Nutrition Examination Survey. (2011) (365)
- Precision Public Health for the Era of Precision Medicine. (2016) (358)
- Uncovering the role of p53 splice variants in human malignancy: a clinical perspective (2013) (357)
- Can family history be used as a tool for public health and preventive medicine? (2002) (355)
- Application of support vector machine modeling for prediction of common diseases: the case of diabetes and pre-diabetes (2010) (345)
- A prospective study of the incidence and natural history of femoral vascular complications after percutaneous transluminal coronary angioplasty. (1991) (343)
- Most Published Research Findings Are False—But a Little Replication Goes a Long Way (2007) (297)
- Big data meets public health (2014) (293)
- Hereditary hemochromatosis: gene discovery and its implications for population-based screening. (1998) (290)
- Impact of violations and deviations in Hardy-Weinberg equilibrium on postulated gene-disease associations. (2006) (283)
- A population study of the VACTERL association: evidence for its etiologic heterogeneity. (1983) (281)
- Informed consent for genetic research on stored tissue samples. (1995) (280)
- Informed consent for population-based research involving genetics. (2001) (278)
- A critical appraisal of the scientific basis of commercial genomic profiles used to assess health risks and personalize health interventions. (2008) (276)
- Recommendations for returning genomic incidental findings? We need to talk! (2013) (275)
- What is the clinical utility of genetic testing? (2006) (266)
- Implications of small effect sizes of individual genetic variants on the design and interpretation of genetic association studies of complex diseases. (2006) (266)
- Periconceptional multivitamin use and the occurrence of conotruncal heart defects: results from a population-based, case-control study. (1996) (257)
- Research priorities for evaluating family history in the prevention of common chronic diseases. (2003) (253)
- A road map for efficient and reliable human genome epidemiology (2006) (252)
- Congenital malformations and intrauterine growth retardation: a population study. (1988) (246)
- The spectrum of congenital anomalies of the VATER association: an international study. (1997) (244)
- Reproducible Research Practices and Transparency across the Biomedical Literature (2016) (243)
- Convergence of Implementation Science, Precision Medicine, and the Learning Health Care System: A New Model for Biomedical Research. (2016) (239)
- Improving Validation Practices in “Omics” Research (2011) (235)
- The Emergence of Translational Epidemiology: From Scientific Discovery to Population Health Impact (2010) (235)
- Prevalence of C282Y and H63D mutations in the hemochromatosis (HFE) gene in the United States. (2001) (230)
- 5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects. (1996) (223)
- Epidemiology of biliary atresia: a population-based study. (1997) (216)
- Commentary: facing the challenge of gene-environment interaction: the two-by-four table and beyond. (2001) (211)
- Delta-aminolevulinic acid dehydratase genotype and lead toxicity: a HuGE review. (2001) (207)
- Family history in public health practice: a genomic tool for disease prevention and health promotion. (2010) (201)
- How many genes underlie the occurrence of common complex diseases in the population? (2005) (197)
- The Scientific Foundation for Personal Genomics: Recommendations from a National Institutes of Health–Centers for Disease Control and Prevention Multidisciplinary Workshop (2009) (196)
- Phenopedia and Genopedia: disease-centered and gene-centered views of the evolving knowledge of human genetic associations (2009) (196)
- Family history of type 2 diabetes: A population-based screening tool for prevention? (2006) (195)
- Contribution of birth defects and genetic diseases to pediatric hospitalizations. A population-based study. (1997) (190)
- Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study. (1996) (188)
- Family History and Prevalence of Diabetes in the U.S. Population (2007) (183)
- Genomic profiling to promote a healthy lifestyle: not ready for prime time (2003) (182)
- Evolving methods in genetic epidemiology. III. Gene-environment interaction in epidemiologic research. (1997) (182)
- Etiologic heterogeneity of neural tube defects: clues from epidemiology. (1982) (181)
- Improving reporting standards for polygenic scores in risk prediction studies (2020) (175)
- The isoforms of the p53 protein. (2010) (173)
- Trends and outcomes after prenatal diagnosis of congenital cardiac malformations by fetal echocardiography in a well defined birth population, Atlanta, Georgia, 1990-1994. (1996) (169)
- The path from genome-based research to population health: Development of an international public health genomics network (2006) (165)
- Improving the prediction of complex diseases by testing for multiple disease-susceptibility genes. (2003) (165)
- Use of Dabigatran for Periprocedural Anticoagulation in Patients Undergoing Catheter Ablation for Atrial Fibrillation (2013) (164)
- Quantifying realistic sample size requirements for human genome epidemiology (2008) (163)
- Does maternal cigarette smoking during pregnancy cause cleft lip and palate in offspring? (1989) (162)
- Do we need genomic research for the prevention of common diseases with environmental causes? (2005) (161)
- Applying public health strategies to primary immunodeficiency diseases: a potential approach to genetic disorders. (2004) (160)
- The surveillance of birth defects: the usefulness of the revised US standard birth certificate. (1996) (160)
- Hemochromatosis-Associated Mortality in the United States from 1979 to 1992: An Analysis of Multiple-Cause Mortality Data (1998) (155)
- Invited commentary: from genome-wide association studies to gene-environment-wide interaction studies--challenges and opportunities. (2008) (154)
- Awareness and utilization of BRCA1/2 testing among U.S. primary care physicians. (2011) (152)
- Future health applications of genomics: priorities for communication, behavioral, and social sciences research. (2010) (151)
- p53 Isoforms: An Intracellular Microprocessor? (2011) (151)
- Case-only design to measure gene-gene interaction. (1999) (149)
- The role of genetic polymorphisms in environmental health. (2003) (148)
- Population-based study of the prevalence of family history of cancer: Implications for cancer screening and prevention (2006) (146)
- The impact of genotype frequencies on the clinical validity of genomic profiling for predicting common chronic diseases (2007) (146)
- Maternal flu, fever, and the risk of neural tube defects: a population-based case-control study. (1994) (145)
- Genome-Wide Association Studies, Field Synopses, and the Development of the Knowledge Base on Genetic Variation and Human Diseases (2009) (144)
- Genetics and Public Health in the 21st Century (2000) (141)
- Genetics and genomics in practice: The continuum from genetic disease to genetic information in health and disease (2003) (137)
- Tracking the epidemiology of human genes in the literature: the HuGE Published Literature database. (2006) (135)
- Surveillance for anencephaly and spina bifida and the impact of prenatal diagnosis--United States, 1985-1994. (1995) (134)
- The Human Genome Epidemiology Network. (1998) (132)
- On the synthesis and interpretation of consistent but weak gene-disease associations in the era of genome-wide association studies. (2007) (132)
- The future of genetic studies of complex human diseases: an epidemiologic perspective. (1998) (131)
- Preconceptional folate intake and malformations of the cardiac outflow tract. Baltimore-Washington Infant Study Group. (1998) (130)
- From genes to public health: the applications of genetic technology in disease prevention. Genetics Working Group. (1995) (129)
- Cascade Screening for Familial Hypercholesterolemia and the Use of Genetic Testing. (2017) (128)
- The epidemiology of medium chain acyl-CoA dehydrogenase deficiency: An update (2006) (128)
- Public Attitudes regarding the Donation and Storage of Blood Specimens for Genetic Research (2001) (126)
- Developing Family Healthware, a Family History Screening Tool to Prevent Common Chronic Diseases (2008) (125)
- From Public Health Emergency to Public Health Service: The Implications of Evolving Criteria for Newborn Screening Panels (2006) (122)
- A network of investigator networks in human genome epidemiology. (2005) (121)
- The evidence dilemma in genomic medicine. (2008) (119)
- Required sample size and nonreplicability thresholds for heterogeneous genetic associations (2008) (119)
- Iron Overload, Public Health, and Genetics: Evaluating the Evidence for Hemochromatosis Screening (1998) (118)
- Will Precision Medicine Improve Population Health? (2016) (117)
- Residential mobility during pregnancy: implications for environmental teratogenesis. (1988) (117)
- DNA Banking for Epidemiologic Studies: A Review of Current Practices (2002) (116)
- Transforming Epidemiology for 21st Century Medicine and Public Health (2013) (116)
- Maternal cigarette smoking and oral clefts: a population-based study. (1987) (115)
- Challenges of translating genetic tests into clinical and public health practice (2009) (115)
- A population approach to precision medicine. (2012) (113)
- The Emergence of Networks in Human Genome Epidemiology: Challenges and Opportunities (2007) (112)
- Population Screening for Genetic Disorders in the 21st Century: Evidence, Economics, and Ethics (2009) (112)
- An epidemiologic assessment of genomic profiling for measuring susceptibility to common diseases and targeting interventions (2004) (111)
- Sample size requirements in case-only designs to detect gene-environment interaction. (1997) (111)
- Duplex scanning-guided thrombin injection for the treatment of iatrogenic pseudoaneurysms. (2002) (109)
- Size matters: just how big is BIG? (2008) (108)
- Family history and prevalence of diabetes in the US population: 6-year results from the National Health and Nutrition Examination Survey (NHANES, 1999 2004). (2007) (108)
- Results of endovascular therapy and aortobifemoral grafting for Transatlantic Inter-Society type C and D aortoiliac occlusive disease. (2008) (107)
- Transmission disequilibrium test (TDT) when only one parent is available: the 1-TDT. (1999) (106)
- Strengthening the reporting of genetic association studies (STREGA): an extension of the strengthening the reporting of observational studies in epidemiology (STROBE) statement. (2009) (105)
- STrengthening the REporting of Genetic Association Studies (STREGA)—an extension of the STROBE statement (2009) (104)
- p53 directly transactivates Δ133p53α, regulating cell fate outcome in response to DNA damage (2011) (104)
- From public health genomics to precision public health: a 20-year journey (2017) (104)
- An epidemiologic approach to ecogenetics. (1988) (103)
- STrengthening the REporting of Genetic Association studies (STREGA) – an extension of the STROBE statement (2009) (103)
- The current state of implementation science in genomic medicine: opportunities for improvement (2017) (103)
- Strengthening the reporting of genetic risk prediction studies: the GRIPS statement (2011) (101)
- The emergence of epidemiology in the genomics age. (2004) (98)
- Mendelian randomisation: a new spin or real progress? (2003) (98)
- The changing epidemiology of neural tube defects. United States, 1968-1989. (1992) (97)
- Risk of childhood cancer for infants with birth defects. I. A record-linkage study, Atlanta, Georgia, 1968-1988. (1993) (97)
- Population study of congenital hypothyroidism and associated birth defects, Atlanta, 1979-1992. (1997) (97)
- p53 mutant breast cancer patients expressing p53γ have as good a prognosis as wild-type p53 breast cancer patients (2011) (97)
- Prevalence in the United States of Selected Candidate Gene Variants (2008) (95)
- Inbreeding and diseases: demographic, genetic, and epidemiologic perspectives. (1991) (92)
- Familial cancer history and chronic lymphocytic leukemia. A case-control study. (1989) (92)
- Epidemiological evaluation of the use of genetics to improve the predictive value of disease risk factors. (1995) (92)
- Health status of Vietnam veterans. III. Reproductive outcomes and child health. The Centers for Disease Control Vietnam Experience Study. (1988) (92)
- Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: summary of a public health/clinical collaborative meeting (2011) (91)
- Extending the reach of public health genomics: What should be the agenda for public health in an era of genome-based and “personalized” medicine? (2010) (90)
- Interpretation of recurring weak associations obtained from epidemiologic studies of suspected human teratogens. (1992) (90)
- Human Genome Epidemiology: A Scientific Foundation for Using Genetic Information to Improve Health and Prevent Disease (2003) (89)
- Assessing value in biomedical research: the PQRST of appraisal and reward. (2014) (88)
- Impact of prenatal diagnosis on the birth prevalence of neural tube defects, Atlanta, 1990-1991. (1995) (87)
- Gene Prospector: An evidence gateway for evaluating potential susceptibility genes and interacting risk factors for human diseases (2008) (87)
- Risk factors for trisomy 21: Maternal cigarette smoking and oral contraceptive use in a spopulation-based case-control study (1999) (86)
- Contribution of different HFE genotypes to iron overload disease: a pooled analysis (2000) (85)
- First-trimester anesthesia exposure and the risk of central nervous system defects: a population-based case-control study. (1994) (82)
- Will Precision Medicine Improve Population Health (2017) (81)
- Genetic analysis of plasma sitosterol, apoprotein B, and lipoproteins in a large Amish pedigree with sitosterolemia. (1986) (80)
- Applications of the case-control method in genetic epidemiology. (1994) (80)
- Health care provider and consumer awareness, perceptions, and use of direct-to-consumer personal genomic tests, United States, 2008 (2009) (80)
- On the use of affected controls to address recall bias in case-control studies of birth defects. (1994) (79)
- Is Family History a Useful Tool for Detecting Children at Risk for Diabetes and Cardiovascular Diseases? A Public Health Perspective (2007) (79)
- A public health perspective on a national precision medicine cohort: balancing long-term knowledge generation with early health benefit. (2015) (79)
- Weak disorder: anomalous transport and diffusion are normal yet again. (2010) (77)
- Etiologic heterogeneity of neural tube defects. II. Clues from family studies. (1982) (76)
- Application of population screening principles to genetic screening for adult-onset conditions. (2001) (76)
- Cardiac sarcoidosis responding to monotherapy with infliximab (2007) (76)
- The Integration of Genomics into Public Health Research, Policy and Practice in the United States (2001) (76)
- Selected midline defect associations: a population study. (1989) (76)
- Current priorities for public health practice in addressing the role of human genomics in improving population health. (2011) (74)
- Personal utility and genomic information: Look before you leap (2009) (74)
- Prevalence and Predictors of Cholesterol Screening, Awareness, and Statin Treatment Among US Adults With Familial Hypercholesterolemia or Other Forms of Severe Dyslipidemia (1999–2014) (2018) (72)
- Strengthening the reporting of genetic association studies (STREGA): an extension of the STROBE Statement (2009) (71)
- Limitations of electroencephalographic monitoring in the detection of cerebral ischemia accompanying carotid endarterectomy. (1991) (71)
- Descriptive epidemiology of small intestinal atresia, Atlanta, Georgia. (1993) (70)
- Increased risk for transverse digital deficiency after chorionic villus sampling: results of the United States Multistate Case-Control Study, 1988-1992. (1995) (69)
- Genetic epidemiology and the future of disease prevention and public health. (1997) (69)
- Dealing With the Evidence Dilemma in Genomics and Personalized Medicine (2010) (69)
- Will genomics widen or help heal the schism between medicine and public health? (2007) (68)
- Translational Research in Cancer Genetics: The Road Less Traveled (2009) (68)
- Personal genomics: information can be harmful (2010) (67)
- Familial risk assessment for early-onset coronary heart disease (2006) (67)
- Prevalence, family history, and prevention of reported osteoporosis in U.S. women. (2008) (67)
- Medium chain acyl‐CoA dehydrogenase deficiency: Human genome epidemiology review (1999) (66)
- Transrenal fixation of aortic stent-grafts for the treatment of infrarenal aortic aneurysmal disease. (2000) (66)
- Evidence-based classification of recommendations on use of genomic tests in clinical practice: Dealing with insufficient evidence (2010) (66)
- The human genome project is complete. How do we develop a handle for the pump? (2003) (66)
- Sensitivity, specificity, and positive predictive value of multiple malformations in isotretinoin embryopathy surveillance. (1990) (64)
- Challenges in communicating genetics: A public health approach (2000) (64)
- The Genomic Applications in Practice and Prevention Network (2009) (63)
- An action plan for translating cancer survivorship research into care. (2014) (63)
- On the ability of birth defects monitoring to detect new teratogens. (1987) (63)
- A systematic review of cancer GWAS and candidate gene meta-analyses reveals limited overlap but similar effect sizes (2013) (63)
- Genetics and genomics in practice: the continuum from genetic disease to genetic information in health and disease. (2003) (63)
- Prevalence of birth defects among low-birth-weight infants. A population study. (1991) (62)
- Contribution of Mendelian disorders to common chronic disease: Opportunities for recognition, intervention, and prevention (2004) (62)
- Family history of heart disease and cardiovascular disease risk-reducing behaviors (2004) (62)
- Collaborative Biomedicine in the Age of Big Data: The Case of Cancer (2014) (62)
- The impact of early cystic fibrosis diagnosis on pulmonary function in children. (2002) (61)
- Human genome epidemiologic reviews: the beginning of something HuGE. (2000) (61)
- Descriptive epidemiology of holoprosencephaly and arhinencephaly in metropolitan Atlanta, 1968-1992. (1996) (60)
- Comparative effectiveness research and genomic medicine: An evolving partnership for 21st century medicine (2009) (60)
- Evaluation of family history as a risk factor and screening tool for detecting undiagnosed diabetes in a nationally representative survey population (2006) (59)
- The case for a global human genome epidemiology initiative (2004) (59)
- Human teratogens, prenatal mortality, and selection bias. (1989) (59)
- Expanding the definition of a positive family history for early-onset coronary heart disease (2006) (58)
- The contribution of maternal epilepsy and its treatment to the etiology of oral clefts: A population based case‐control study (1994) (58)
- Awareness and use of direct-to-consumer nutrigenomic tests, United States, 2006 (2007) (58)
- The effect of genetic susceptibility on causal inference in epidemiologic studies. (1987) (57)
- Early diagnosis of cystic fibrosis in the newborn period and risk of Pseudomonas aeruginosa acquisition in the first 10 years of life: A registry-based longitudinal study. (2001) (57)
- Family history score as a predictor of breast cancer mortality: prospective data from the Cancer Prevention Study II, United States, 1982-1991. (1998) (57)
- Proceedings from the 9th annual conference on the science of dissemination and implementation (2017) (57)
- Clinical-epidemiologic assessment of pattern of birth defects associated with human teratogens: application to diabetic embryopathy. (1989) (57)
- Risk of childhood cancer for infants with birth defects. II. A record-linkage study, Iowa, 1983-1989. (1993) (57)
- Paternal effects on the human sex ratio at birth: evidence from interracial crosses. (1984) (56)
- Influence of arterial access sites and interventional procedures on vascular complications after cardiac catheterizations. (1992) (56)
- Health-Related Direct-to-Consumer Genetic Tests: A Public Health Assessment and Analysis of Practices Related to Internet-Based Tests for Risk of Thrombosis (2008) (56)
- Limb defects associated with major congenital anomalies: clinical and epidemiological study from the International Clearinghouse for Birth Defects Monitoring Systems. (2000) (55)
- Improved ascertainment of cardiovascular malformations in infants with Down's syndrome, Atlanta, 1968 through 1989. Implications for the interpretation of increasing rates of cardiovascular malformations in surveillance systems. (1992) (55)
- The probiotic E. coli strain Nissle 1917 for the treatment of collagenous colitis: first results of an open-label trial. (2004) (55)
- Is maternal obesity a risk factor for anencephaly and spina bifida (1996) (55)
- Population and familial relative risks of disease associated with environmental factors in the presence of gene-environment interaction. (1993) (55)
- Trends and patterns of mortality associated with birth defects and genetic diseases in the United States, 1979–1992: An analysis of multiple‐cause mortality data (1997) (55)
- Prospective study of methylenetetrahydrofolate reductase (MTHFR) variant C677T and risk of all-cause and cardiovascular disease mortality among 6000 US adults. (2012) (55)
- Public health impact of genetic tests at the end of the 20th century (2001) (54)
- The interaction between dysmorphology and epidemiology: methodologic issues of lumping and splitting. (1992) (54)
- Public Health Action in Genomics Is Now Needed beyond Newborn Screening (2012) (54)
- Maternal thyroid disease and risk of birth defects in offspring: a population-based case-control study. (1989) (54)
- Contribution of birth defects to infant mortality among racial/ethnic minority groups, United States, 1983. (1990) (53)
- Human Genome Sequencing at the Population Scale: A Primer on High-Throughput DNA Sequencing and Analysis (2017) (53)
- On the measurement of susceptibility in epidemiologic studies. (1989) (53)
- An epidemiologic approach to the evaluation of the effect of inbreeding on prereproductive mortality. (1987) (52)
- Beyond base pairs to bedside: a population perspective on how genomics can improve health. (2012) (52)
- Evaluation of the validity and utility of genetic testing for rare diseases. (2010) (52)
- Elevated midtrimester serum methylmalonic acid levels as a risk factor for neural tube defects. (1995) (52)
- Ectopia cordis, midline defects and chromosome abnormalities: an epidemiologic perspective. (1988) (51)
- Making genomic medicine evidence-based and patient-centered: a structured review and landscape analysis of comparative effectiveness research (2017) (51)
- How can polygenic inheritance be used in population screening for common diseases? (2013) (51)
- Transcatheter aortic valve implantation, patient selection process and procedure: two centres' experience of the intervention without general anaesthesia. (2010) (51)
- The Relation of Computer-Based Measures of Sperm Morphology and Motility to Male Infertility (1992) (51)
- Predictive genetic testing for type 2 diabetes (2006) (51)
- Population Sciences, Translational Research, and the Opportunities and Challenges for Genomics to Reduce the Burden of Cancer in the 21st Century (2011) (50)
- Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration (2011) (50)
- Charting a future for epidemiologic training. (2015) (50)
- Prioritizing Genomic Applications for Action by Level of Evidence: A Horizon‐Scanning Method (2014) (49)
- Results of iliac stenting and aortofemoral grafting for iliac artery occlusions. (2013) (49)
- Epidemiology of birth defects. (1989) (49)
- Reducing the burden of disease and death from familial hypercholesterolemia: a call to action. (2014) (49)
- Monitoring for multiple congenital anomalies: an international perspective. (1994) (48)
- GAPscreener: An automatic tool for screening human genetic association literature in PubMed using the support vector machine technique (2008) (48)
- Does light-to-moderate alcohol consumption during pregnancy increase the risk for renal anomalies among offspring? (1997) (48)
- Public awareness and use of direct-to-consumer genetic tests: results from 3 state population-based surveys, 2006. (2009) (48)
- Steroid 5-{alpha}-reductase Type 2 (SRD5a2) gene polymorphisms and risk of prostate cancer: a HuGE review. (2010) (47)
- Cancer Pharmacogenomics and Pharmacoepidemiology: Setting a Research Agenda to Accelerate Translation (2010) (47)
- Precision Public Health as a Key Tool in the COVID-19 Response. (2020) (47)
- Inbreeding and prereproductive mortality in the Old Order Amish. I. Genealogic epidemiology of inbreeding. (1987) (47)
- Evaluation of birth defect histories obtained through maternal interviews. (1990) (46)
- Differences in the epidemiology of prematurity and intrauterine growth retardation. (1986) (46)
- Public awareness and use of direct-to-consumer personal genomic tests from four state population-based surveys, and implications for clinical and public health practice (2012) (45)
- On the measurement and interpretation of birth defect associations in epidemiologic studies. (1990) (45)
- Maternal factors in cleft lip with or without palate: evidence from interracial crosses in the United States. (1983) (45)
- The Geometric Increase in Meta-Analyses from China in the Genomic Era (2013) (45)
- Clinical presentation and treatment of cardiac myxoma in 153 patients (2018) (45)
- Recommendations and proposed guidelines for assessing the cumulative evidence on joint effects of genes and environments on cancer occurrence in humans. (2012) (45)
- Epigenetic Research in Cancer Epidemiology: Trends, Opportunities, and Challenges (2013) (44)
- Does Genetic Testing Really Improve the Prediction of Future Type 2 Diabetes? (2006) (44)
- Trends in Utilization and Costs of BRCA Testing among Women Aged 18–64 Years in the United States, 2003–2014 (2017) (44)
- BRCA Genetic Testing and Receipt of Preventive Interventions Among Women Aged 18–64 Years with Employer-Sponsored Health Insurance in Nonmetropolitan and Metropolitan Areas — United States, 2009–2014 (2017) (44)
- Reporting of Human Genome Epidemiology (HuGE) association studies: An empirical assessment (2008) (43)
- Horizon scanning for new genomic tests (2011) (43)
- “Drivers” of Translational Cancer Epidemiology in the 21st Century: Needs and Opportunities (2013) (43)
- Multilevel research and the challenges of implementing genomic medicine. (2012) (43)
- Evaluation of the potential excess of statistically significant findings in published genetic association studies: application to Alzheimer's disease. (2008) (43)
- Increased frequency of cystic fibrosis among infants with jejunoileal atresia. (1998) (43)
- Epidemiologic evaluation of screening for risk factors: application to genetic screening. (1985) (42)
- Case-parental control method in the search for disease-susceptibility genes. (1994) (41)
- Does periconceptional multivitamin use reduce the risk of neural tube defects associated with other birth defects? data from two population-based case-control studies. (1996) (40)
- Recurrence of low birth weight in siblings. (1989) (40)
- A case-control study of maternal alcohol consumption and intrauterine growth retardation. (2001) (40)
- The Impact of Genomics on Public Health Practice: The Case for Change (2012) (39)
- The HuGENetTM HuGE Review Handbook, version 1.0 (2006) (39)
- Is there etiologic heterogeneity between upper and lower neural tube defects? (1992) (39)
- Preemployment screening for allergy to laboratory animals: epidemiologic evaluation of its potential usefulness. (1986) (39)
- A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health (2018) (39)
- The association between family history of asthma and the prevalence of asthma among US adults: National Health and Nutrition Examination Survey, 1999–2004 (2009) (38)
- Family history and personal genomics as tools for improving health in an era of evidence-based medicine. (2010) (38)
- Population-Based Precision Cancer Screening: A Symposium on Evidence, Epidemiology, and Next Steps (2016) (38)
- Imaging and counting threading dislocations in c-oriented epitaxial GaN layers (2013) (38)
- Completeness of the discharge diagnoses as a measure of birth defects recorded in the hospital birth record. (1991) (38)
- Genome-wide association studies in pharmacogenomics: untapped potential for translation (2009) (38)
- A Proposed Approach for Implementing Genomics-Based Screening Programs for Healthy Adults (2018) (37)
- Human genome epidemiology : building the evidence for using genetic information to improve health and prevent disease (2010) (37)
- Adolescents with severe obesity: outcomes of participation in an intensive obesity management programme (2015) (37)
- Communication of cancer-related genetic and genomic information: A landscape analysis of reviews. (2018) (37)
- Surgical treatment of primary intracardiac myxoma: 19 years of experience. (2011) (37)
- Strengthening the reporting of genetic risk prediction studies: the GRIPS statement. (2011) (37)
- Genomics and the Prevention and Control of Common Chronic Diseases: Emerging Priorities for Public Health Action (2005) (36)
- TP53 drives invasion through expression of its Δ133p53β variant (2016) (36)
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- Cavity-enhanced zero-phonon emission from an ensemble of G centers in a silicon-on-insulator microring (2022) (3)
- The probiotic E. coli strain Nissle 1917 for the treatment of collagenous colitis: First results of an open labeled trial# (2003) (3)
- Multiple Giant Coronary Artery Aneurysms Surgically Treated with Bypass Grafting: A Challenging Rarity (2018) (2)
- Challenges and Opportunities for Communication about the Role of Genomics in Public Health (2021) (2)
- Cardiac cavernous haemangioma: diagnosis and treatment (2014) (2)
- Commentary: contributions of epidemiology to the study of birth defects in humans. (1995) (2)
- Mutation detection in the ABCC6 gene and analysis in a large international cohort affected by pseudoxanthoma elasticum (2007) (2)
- Combining molecular and genetic data from different sources. (2011) (2)
- Gestational age and intrauterine growth retardation among white and black very low birthweight infants: a population-based cohort study. (1994) (2)
- Growth rate of an apical left ventricular myxoma using serial two dimensional echocardiographic and computed tomography observations over twelve months: a case report (2014) (2)
- Reply to Stephan et al. (2008) (2)
- Evaluation of predictive genetic tests for common diseases: Bridging epidemiological, clinical, and public health measures (2010) (2)
- Reviewer Acknowledgment (2013) (2)
- Tracking human genes along the translational continuum (2019) (2)
- Erratum: Correction: A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health (PLoS medicine (2018) 15 8 (e1002631)) (2018) (2)
- Cardiac electrophysiology in Lebanon. (2010) (2)
- Knowledge Gaps Remain in the Use of Family Health History in Public Health (2010) (2)
- Why a special issue on atrial fibrillation? (2013) (2)
- The use of family history in public health practice: the epidemiologic view (2009) (2)
- Evaluating the role of public health in implementation of genomics-related recommendations: a case study of hereditary cancers using the CDC Science Impact Framework (2018) (2)
- Response to Letter by May et al regarding article, "Use of dabigatran for periprocedural anticoagulation in patients undergoing catheter ablation for atrial fibrillation" by Bassiouny et al. (2013) (2)
- Correspondence to Sand et al. “Critical Reappraisal of a Catechol-O-Methyltransferase Transversion Variant in Schizophrenia” (2010) (2)
- From Genes to Public Health: The Applications of Genetic Technology in Disease Prevention (2018) (2)
- D133P53, directly transactivated by p53, prevents p53-mediated apoptosis without inhibiting p53-mediated cell cycle arrest (2010) (2)
- (Mis)classifying limb deficiencies: Reply to "Academicians are more likely to share each other's toothbrush than each other's nomenclature (Cohen, 1982)". (1998) (2)
- Addressing the routine failure to clinically identify monogenic cases of common disease (2022) (2)
- Cancer Epidemiology in the 21 st Century " Drivers " of Translational Cancer Epidemiology in the 21 st Century : Needs and Opportunities (2013) (2)
- The atrial FibriLlatiOn real World management registry in the Middle East and Africa: design and rationale (2020) (2)
- Mechanisms of sequential ion-molecule reactions in protonated methanol (2019) (2)
- A genealogic study of inbreeding and prereproductive mortality in the old order Amish (1986) (2)
- Genomic and Proteomic Study of the Inflammatory Pathway in Patients With Atrial Fibrillation and Cardiometabolic Syndrome (2017) (2)
- Steroid 5-a-Reductase Type 2 ( SRD 5 a 2 ) Gene Polymorphisms and Risk of Prostate Cancer : A HuGE Review (2009) (2)
- Myelomeningocele and necrotizing enterocolitis. (1989) (2)
- Genomic, Personalized Medicine and Public Health (2013) (2)
- Cox‐maze procedure for treatment of atrial flutter associated with an atrial septal defect (2000) (1)
- Prevalence of Genetic Variants in the United States: Results from the Third National Health and Nutrition Examination Survey (NHANES III), 1991-1994 (1994) (1)
- COVID-19-Related manuscripts: lag from preprint to publication (2022) (1)
- Are randomized trials obsolete or more important than ever in the genomic era? (2013) (1)
- Ultrasound-guided Thrombin Injection of an AVF Pseudoaneurysm (2000) (1)
- When Does a Difference Make a Difference? (2010) (1)
- Introduction to the 4th National Conference on Genomics and Public Health (2012) (1)
- Evaluating Precision Medicine's Ability to Improve Population Health-Reply. (2017) (1)
- COVID-19 GPH: tracking the contribution of genomics and precision health to the COVID-19 pandemic response (2022) (1)
- A Confused Pacemaker. (2016) (1)
- Cancer and family history : using genomics for prevention (2016) (1)
- Looking back at genomic medicine in 2011 (2012) (1)
- Building a knowledge base on genetic variation and cancer risk through field synopses. (2009) (1)
- The Cancer Genomics and Epidemiology Navigator: An NCI Online Tool to Enhance Cancer Epidemiology Research (2014) (1)
- Passive smoking: A reply (1991) (1)
- The Cancer Epidemiology Descriptive Cohort Database: A Tool to Support Population-Based Interdisciplinary Research (2016) (1)
- Lethal Injection: Other Views (2007) (1)
- PREVALENCE OF BIRTH DEFECTS AMONG LBW INFANTS. A POPULATION STUDY (1991) (1)
- Long-Term Results after Modified Bentall Operation in 200 Patients. (2017) (1)
- Atrial fibrillation in the WPW syndrome during pregnancy. (2000) (1)
- Graves' disease presentation after covid-19 infection (2021) (1)
- Ablation of an orthodromic reentrant tachycardia via a concealed accessory pathway targeted in the non-coronary sinus (2015) (1)
- Vitamin A and birth defects. (1996) (1)
- Isolated dextrocardia and congenital heart blocking (2015) (1)
- National Office of Public Health Genomics Coordinating Center for Health Promotion Centers for Disease Control and Prevention (2007) (1)
- A Population Study of the VACTERL Association: Evidence for Its Etiologic Heterogeneity (1983) (1)
- Polymorphisms of adrenergic receptors and the risk of heart failure. (2003) (1)
- A New Resource for Genomics and Precision Health Information and Publications on the Investigation and Control of COVID-19 and other Coronaviruses (2020) (1)
- Evidence Dilemma: The Authors Respond (2009) (1)
- Evaluating the Clinical Utility of Genomic Variants Derived from Next-Generation Sequencing for Opportunistic Disease Screening and Risk Assessment: Evidence Gaps and Priorities (2015) (1)
- The Public Health Role in Translating Advances in Genomics (2014) (1)
- Abstract #1017450: COVID-19 Associated Grave’s Disease Identified in a 45-year-old Male (2021) (1)
- Predictors of high trust and the role of confidence levels in seeking cancer-related information (2021) (1)
- Predictive Analytics (2019) (1)
- An Epidemiologic Approach toEcogenetics (1988) (1)
- COVID-19 Scientific Publications From the Centers for Disease Control and Prevention, January 2020–January 2022 (2022) (0)
- Reconstruction of the Standard Electrocardiogram From Recording Using Modified Limb Lead Positions for Wolf-Parkinson-White (WPW) Syndrome Diagnosis (2005) (0)
- HLBS-PopOmics: an online knowledge base to accelerate dissemination and implementation of research advances in population genomics to reduce the burden of heart, lung, blood, and sleep disorders (2018) (0)
- 259 Atopy as a screening criterion for employment; an epidemiologic evaluation (1985) (0)
- Epidemiology matters: peering inside the “black box” in economic evaluations of genetic testing (2016) (0)
- Hemochromatosis: Evidence for population-based testing for hemochromatosis (2000) (0)
- Cardiac Electrophysiology in Lebanon—Part II (2013) (0)
- Extraction of a tunneled jugular defibrillator lead via a superior approach. (2014) (0)
- A Software detector of the Wolff‐Parkinson‐White (WPW) Syndrome (2000) (0)
- THE INTERFACE OF EPIDEMIOLOGIC METHODS Interface of Genetics and Epidemiology (2005) (0)
- Translation research is an essential but not sufficient ingredient for translation of genomic medicine into population health benefits (2009) (0)
- Will genetics revolutionize medicine? (2000) (0)
- The Joint Public Health Impact of Family History of Diabetes and Cardiovascular Disease among Adults in the United States: A Population-Based Study (2022) (0)
- Tying the knot: An uncommon complication (2019) (0)
- Human Genome Epidemiology (HuGE) Review Steroid 5-a-Reductase Type 2 (SRD5a2) Gene Polymorphisms and Risk of Prostate Cancer: A HuGE Review (2009) (0)
- STREGA Reporting Recommendations, Extended from STROBE Statement (2009) (0)
- BeyondBasePairstoBedside:APopulationPerspectiveon HowGenomicsCanImproveHealth (2012) (0)
- Subject Index Vol. 9, 2006 (2006) (0)
- for Renal Anomalies Among Offspring? Does Light-to-Moderate Alcohol Consumption During Pregnancy Increase the Risk (2013) (0)
- Contents Vol. 22, 2019 (2020) (0)
- Title Neuraminidase antibodies and H 5 N 1 : Geographic-dependent influenza epidemiology could determine cross-protection against emerging strains (2007) (0)
- Cost-Effective Regression Testing (2006) (0)
- Genetics and Genomics in Public Health (2019) (0)
- An epidemiologic assessment of the relationship between the G985A medium chain acyl-coA dehydrogenase deficiency (MCADD) allelic variant and sudden infant death syndrome (SIDS) (1999) (0)
- Rewriting the Twentieth-century French Literary Right: Translation, Ideology, and Literary History (2017) (0)
- Evaluation of Family History as a Screening Tool for Detecting Undiagnosed Diabetes (2006) (0)
- The impact of genomics on precision public health: beyond the pandemic (2021) (0)
- Communication About Hereditary Cancers on Social Media: A Content Analysis of Tweets About Hereditary Breast and Ovarian Cancer and Lynch Syndrome (2018) (0)
- Appendix 3: Parkinson’s Disease: Environmental and Genetic Risk Factors (2013) (0)
- Erratum: Stakeholder assessment of the evidence for cancer genomic tests: Insights from three case studies (Genetics in Medicine (2012) 14 (656-662) DOI: 10.1038/gim.2012.3) (2013) (0)
- Trends in published meta-analyses in cancer research, 2008–2013 (2016) (0)
- Difference Make a Difference? Assessment of Improved Prediction Beyond Traditional Risk Factors : When Does a (2012) (0)
- 2012 highlights in translational 'omics (2013) (0)
- Abstract 035: Prevalence and Predictors of Cholesterol Screening, Awareness, and Statin Treatment Among Individuals With Familial Hypercholesterolemia in the U.S. (1999-2014) (2018) (0)
- Results of Iliac Stenting for Iliac Artery Occlusions (2011) (0)
- Rupture of Abdominal Aortic and Iliac Aneurysms in Patients With and Without Antecedent Endovascular Repair (2015) (0)
- Technical considerations in endovascular repair of large symptomatic iliac anastomotic aneurysms. (2007) (0)
- Correction to: Communication about Hereditary Cancers on Social Media: a Content Analysis of Tweets about Hereditary Breast and Ovarian Cancer and Lynch Syndrome (2020) (0)
- Performance Assessment of the C-Mod Multi-Spectral Line Polarization MSE (MSE-MSLP) Diagnostic (2015) (0)
- Ten years of Genome Medicine (2019) (0)
- Silicon quantum dots in a metal-oxide semiconductor structure (1999) (0)
- Posttraumatic Treatment Interventions for Refugee Children Residing in the Middle East and North Africa (MENA) Region: A Brief Review (2022) (0)
- Superfluous Amylase/lipase Testing at University-Affiliated Teaching Hospital: Retrospective Review: Presidential Poster Award (2018) (0)
- Superfluous Amylase/Lipase Testing at a University-Affiliated Teaching Hospital: A Retrospective Review (2019) (0)
- Serum Amylase Added Value to Non-Diagnostic Serum Lipase in Acute Pancreatitis: Retrospective Study (2018) (0)
- Sa1377 – Reduction in Amylase/Lipase Superfluous Testing: A Quality Improvement Study (2019) (0)
- Lam et al. respond to "Driving for further evolution". (2015) (0)
- A program planning design for a physical education curriculum, grades K-6, for American-Sponsored Overseas schools, specifically Spain (1986) (0)
- Evaluating data from newborn screening programs - Georgia, 1998 (2000) (0)
- Emerging Precision Medicine Concepts and Cardiovascular Health in African Americans and Hispanics (2021) (0)
- Using case‐control designs for genome‐wide screening for associations between genetic markers and disease susceptibility loci (1999) (0)
- From genomic medicine to precision medicine: highlights of 2015 (2016) (0)
- Public Health Genomics (2011) (0)
- 2.4 Genomics and public health (2009) (0)
- PublicAwarenessandUse ofDirect-to-Consumer GeneticTests:Results From3StatePopulation- BasedSurveys,2006 (2009) (0)
- A public health approach to pharmacogenomics and gene-based diagnostic tests – PERSPECTIVE (2006) (0)
- Trends in Clinical Characteristics (2016) (0)
- Genetics and Public Health in 2121 Century: A Scientific Foundation for Using Genetic Information to Improve Health and Prevent Discease? (2000) (0)
- Translational Genomic Epidemiology: From the Science of Discovery to the Science of Action (2012) (0)
- Editorial: DNA-based population screening for precision public health (2022) (0)
- in economic evaluations of genetic testing (2016) (0)
- Abstract 254: How can epidemiology become more effective in reducing the burden of cancer in the 21stcentury? An analysis of NCI-funded grants and the scientific literature (2014) (0)
- Front & Back Matter (2012) (0)
- Current status of the implementation of gene expression testing in breast cancer management in the United States. (2013) (0)
- 14 – Genetic Disease (1993) (0)
- Genomics and public health research. Authors' reply (2007) (0)
- The integration of genomics into paediatric and perinatal epidemiology: guidelines for submitting human genome epidemiology (HuGE) reviews. (2005) (0)
- Training the Twenty-First Century Cancer Epidemiologist (2018) (0)
- Contents Vol. 9, 2006 (2006) (0)
- Appendix 2: The Calculus of the Decision Theoretic Framework (DTF) (2013) (0)
- Reply to Dr. Hook (1990) (0)
- Translating Genomic Advances (2014) (0)
- an action Plan f or t ranslating Cancer Sur vivorship r esearch Into Care (2014) (0)
- Cancer Epidemiology Consortia Network Analysis (2013) (0)
- Abstract LB-195: Supporting cancer epidemiology research through cohort registration: NCI's cancer epidemiology cohort descriptive database (2015) (0)
- Newborn screening for sickle cell disease: assessing program effectiveness (2000) (0)
- Authors' response to a refinement to ‘how many genes underlie the occurrence of common complex diseases in the population?’ by Ramal Moonesinghe (2006) (0)
- Contents Vol. 13, 2010 (2010) (0)
- Abstract 3698: The landscape of published cancer meta-analyses: a descriptive look from 2008-2013 (2015) (0)
- On the use of population attributable fraction to estimate sample size required in case-control study of gene-environment interaction (2001) (0)
- CORRIGENDUM: Stakeholder assessment of the evidence for cancer genomic tests: insights from three case studies (2013) (0)
- The authors reply. (2015) (0)
- Using Precision Medicine to Improve Health and Healthcare (2018) (0)
- Meta-Analysis Evaluation of the Potential Excess of Statistically Significant Findings in Published Genetic Association Studies : Application to Alzheimer ’ s Disease (2008) (0)
- HuGE Reviews and Meta-analysis of Gene Association Studies (2007) (0)
- Evolutionary Conservation Genetics (2020) (0)
- Data for: Redundant meta-analyses are common in genetic epidemiology (2020) (0)
- Method of Estimating Sodium Intake and Its Possible Influence on NHANES III Outcome—Reply (2011) (0)
- Subject Index Vol. 13, 2010 (2010) (0)
- Contents Vol. 15, 2012 (2012) (0)
- CHAPTER 40 – Principles of Human Genome Epidemiology (2009) (0)
- Epidemiology in the 21 st Century : the Model of Cancer Consortia (2013) (0)
- CHAPTER 39 – Why Do We Need Public Health in the Era of Genomic Medicine? (2009) (0)
- Addressing the routine failure to clinically identify monogenic cases of common disease (2022) (0)
- Public Health Genomics: Using Genetic Information to Improve Health Now and in the Future (2012) (0)
- Cancer Epidemiology in the 21 st Century Transforming Epidemiology for 21 st Century Medicine and Public Health (2013) (0)
- Appendix 1: Using Austin Bradford Hill’s Guidelines in Genetics and Genomics (2013) (0)
- Arabic, as a Home Language, Acts as a Resource in an English Writing Class: Borrowing Translation Strategies in a First Year Writing Course (2020) (0)
- The Growth and Development of a Discipline: Review of Three Books on Reproductive and Perinatal Epidemiology (1992) (0)
- Guidelines for submitting human genome epidemiology (HuGE) reviews to Teratology (2001) (0)
- Q&A: Muin Khoury on cancer epidemiology. (2014) (0)
- Agent Orange as a Cause of Spina Bifida (2017) (0)
- Atrial fibrillation and stroke: risk stratification and new anticoagulants. (2013) (0)
- Abstract PL03-02: Public health genomics: A scientific foundation for using genetic information in cancer prevention (2010) (0)
- INVESTIGATION OF CARDIAC ARRHYTHMIAS IN CANCER PATIENTS TREATED WITH THORACIC RADIOTHERAPY (2022) (0)
- WHOLE EXOME SEQUENCING OF THREE PATIENTS WITH BRUGADA SYNDROME IN THE MIDDLE EAST- NOVEL VARIANTS IN KNOWN GENES IN RELATION TO A RANGE OF PHENOTYPES (2021) (0)
- PP-136 [AJC » Arrhythmias and antiarrhythmic therapy] Arrhythmia and Impact on Patient's Life (2017) (0)
- Cancer communication research in the era of genomics and precision medicine: a scoping review (2018) (0)
- Genetic Analysis ofPlasmaSitosterol, Apoprotein B, andLipoproteins inaLargeAmishPedigree withSitosterolemia (1986) (0)
- Epidemiology: The logic of medicine, Milos Jenicek. Montreal: EPIMED International, 1995 (1995) (0)
- HIGH INCIDENCE OF STEAM POP FORMATION WITH THERAPY COOL FLEX RF ABLATION CATHETER (2019) (0)
- Establishing Safe Working Parameters for Radiofrequency Ablation In Vitro Using Acoustic Sensing, Probability Mapping, and Catheter Contact Angle (2022) (0)
- Non-familial cardiomyopathies in Lebanon: exome sequencing results for five idiopathic cases (2019) (0)
- NationalInstitutesofHealthApproachestoDisseminationand ImplementationScience:CurrentandFutureDirections (2012) (0)
- A medical mystery--palpitations. (2014) (0)
- TARGETED AND EXOME SEQUENCING OF 27 LEBANESE PATIENTS WITH CARDIOMYOPATHIES: NOVEL VARIANTS IN KNOWN GENES, AND POTENTIAL NOVEL GENES (2017) (0)
- Khoury et al. Reply (2011) (0)
- OP-069 [AJC » Cardiac Resynchronization Therapy] Cardiac Implantable Electronic Device (CIED) Infections in a Tertiary Care Center in Lebanon (2017) (0)
- Incessant Long R-P Tachycardia. (2012) (0)
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