Augustine Kong
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Biology
Augustine Kong's Degrees
- PhD Genetics University of Oxford
- Masters Bioinformatics Imperial College London
Why Is Augustine Kong Influential?
(Suggest an Edit or Addition)According to Wikipedia, Chung Tung Augustine Kong is a statistical geneticist who is Professor of Statistical Genetics at the University of Oxford's Nuffield Department of Medicine, where he is also the Senior Group Leader in Genomic Epidemiology. He was previously the head of the statistics team at the Icelandic company deCODE genetics, and before that, he taught at the University of Chicago. He has conducted research on the genetic basis of educational attainment and the way in which it can be influenced by "genetic nurture", or the genes carried by parents but not passed on to their children.
Augustine Kong'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
- Finding the missing heritability of complex diseases (2009) (7749)
- Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes (2006) (2206)
- New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (2010) (2087)
- Variant of TREM2 associated with the risk of Alzheimer's disease. (2013) (2004)
- Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (2008) (1882)
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) (1839)
- Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) (1801)
- Large recurrent microdeletions associated with schizophrenia (2008) (1790)
- A high-resolution recombination map of the human genome (2002) (1763)
- Rate of de novo mutations and the importance of father’s age to disease risk (2012) (1720)
- Neuregulin 1 and susceptibility to schizophrenia. (2002) (1657)
- Common variants conferring risk of schizophrenia (2009) (1653)
- Missing heritability and strategies for finding the underlying causes of complex disease (2010) (1643)
- A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline (2012) (1519)
- A variant associated with nicotine dependence, lung cancer and peripheral arterial disease (2008) (1503)
- Genetics of gene expression and its effect on disease (2008) (1345)
- Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity (2009) (1344)
- Sequential Imputations and Bayesian Missing Data Problems (1994) (1164)
- Genome-wide association study identifies 74 loci associated with educational attainment (2016) (1114)
- A variant in CDKAL1 influences insulin response and risk of type 2 diabetes (2007) (1066)
- Allele-sharing models: LOD scores and accurate linkage tests. (1997) (1035)
- A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction (2007) (1013)
- The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke (2004) (960)
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) (933)
- Variants conferring risk of atrial fibrillation on chromosome 4q25 (2007) (910)
- Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24 (2007) (904)
- Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease (2011) (894)
- Allegro, a new computer program for multipoint linkage analysis (2000) (802)
- A common variant on chromosome 9p21 affects the risk of myocardial infarction. (2007) (795)
- Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction (2009) (790)
- Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor–positive breast cancer (2007) (787)
- The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm (2008) (765)
- Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes (2007) (765)
- A common inversion under selection in Europeans (2005) (760)
- Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways (2012) (758)
- Mapping cis- and trans-regulatory effects across multiple tissues in twins (2012) (754)
- Variants in MTNR1B influence fasting glucose levels (2009) (742)
- Common Sequence Variants in the LOXL1 Gene Confer Susceptibility to Exfoliation Glaucoma (2007) (690)
- Twenty bone mineral density loci identified by large-scale meta-analysis of genome-wide association studies (2009) (687)
- Many sequence variants affecting diversity of adult human height (2008) (664)
- Covariance structure of the Gibbs sampler with applications to the comparisons of estimators and augmentation schemes (1994) (642)
- Large-scale whole-genome sequencing of the Icelandic population (2015) (638)
- Multiple genetic loci for bone mineral density and fractures. (2008) (632)
- A common variant associated with prostate cancer in European and African populations (2006) (630)
- The nature of nurture: Effects of parental genotypes (2017) (618)
- Sequence variants at the TERT-CLPTM1L locus associate with many cancer types (2009) (613)
- The gene encoding phosphodiesterase 4D confers risk of ischemic stroke (2003) (602)
- Association of neuregulin 1 with schizophrenia confirmed in a Scottish population. (2003) (581)
- Parental origin of sequence variants associated with complex diseases (2009) (573)
- Fine-scale recombination rate differences between sexes, populations and individuals (2010) (551)
- An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans (2017) (547)
- Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (516)
- Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution (2007) (515)
- Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly. (2017) (493)
- Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer (2008) (490)
- A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke (2009) (466)
- Detection of sharing by descent, long-range phasing and haplotype imputation (2008) (441)
- Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (421)
- Sequence variant on 8q24 confers susceptibility to urinary bladder cancer (2008) (410)
- Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans (1999) (410)
- Loss-of-function mutations in SLC30A8 protect against type 2 diabetes (2014) (405)
- Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations (2009) (393)
- Several common variants modulate heart rate, PR interval and QRS duration (2010) (391)
- Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
- A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction (2006) (383)
- Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility (2009) (360)
- Mutations in BRIP1 confer high risk of ovarian cancer (2011) (350)
- Genetic fine-mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci (2015) (349)
- Two newly identified genetic determinants of pigmentation in Europeans (2008) (349)
- New sequence variants associated with bone mineral density (2009) (345)
- Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer (2008) (337)
- ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma (2008) (335)
- Parental influence on human germline de novo mutations in 1,548 trios from Iceland (2017) (325)
- New common variants affecting susceptibility to basal cell carcinoma (2009) (321)
- Polygenic risk scores for schizophrenia and bipolar disorder predict creativity (2015) (317)
- Identification of an imprinted master trans-regulator at the KLF14 locus related to multiple metabolic phenotypes (2011) (316)
- A direct characterization of human mutation based on microsatellites (2012) (310)
- Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma (2010) (296)
- A genetic risk factor for periodic limb movements in sleep. (2007) (295)
- Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes (2014) (294)
- A rare variant in MYH6 is associated with high risk of sick sinus syndrome (2011) (294)
- Familial aggregation of Parkinson's disease in Iceland. (2000) (292)
- Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke (2008) (284)
- Cancer as a Complex Phenotype: Pattern of Cancer Distribution within and beyond the Nuclear Family (2004) (278)
- Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease (2015) (275)
- Collaborative Meta-analysis: Associations of 150 Candidate Genes With Osteoporosis and Osteoporotic Fracture (2009) (267)
- Mapping of a familial essential tremor gene, FET1, to chromosome 3q13 (1997) (264)
- Linkage of Osteoporosis to Chromosome 20p12 and Association to BMP2 (2003) (263)
- A germline variant in the TP53 polyadenylation signal confers cancer susceptibility (2011) (261)
- Rate of de novo mutations, father’s age, and disease risk (2012) (258)
- Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density (2009) (256)
- Genome-wide analysis identifies 12 loci influencing human reproductive behavior (2016) (250)
- Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits (2013) (249)
- Association between the gene encoding 5-lipoxygenase-activating protein and stroke replicated in a Scottish population. (2005) (245)
- CFH Y402H Confers Similar Risk of Soft Drusen and Both Forms of Advanced AMD (2005) (238)
- Inheritance of human longevity in Iceland (2000) (230)
- Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease (2011) (228)
- A susceptibility gene for late‐onset idiopathic Parkinson's disease (2002) (222)
- Effects of a 5-lipoxygenase-activating protein inhibitor on biomarkers associated with risk of myocardial infarction: a randomized trial. (2005) (221)
- Localization of a susceptibility gene for common forms of stroke to 5q12. (2002) (219)
- Genetic factors contribute to the risk of developing endometriosis. (2002) (218)
- Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche (2009) (213)
- Common variants at VRK2 and TCF4 conferring risk of schizophrenia. (2011) (210)
- A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13. (1999) (208)
- Discovery of common variants associated with low TSH levels and thyroid cancer risk (2012) (207)
- Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2. (2003) (206)
- Variant in the sequence of the LINGO1 gene confers risk of essential tremor (2009) (204)
- Sequence Variants in the RNF212 Gene Associate with Genome-Wide Recombination Rate (2008) (203)
- A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1–1q1 (1994) (201)
- Allegro version 2 (2005) (199)
- Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm (2010) (197)
- Genomewide scan for hand osteoarthritis: a novel mutation in matrilin-3. (2003) (193)
- Identification of a large set of rare complete human knockouts (2015) (192)
- Recombination rate and reproductive success in humans (2004) (191)
- Single-Tissue and Cross-Tissue Heritability of Gene Expression Via Identity-by-Descent in Related or Unrelated Individuals (2011) (189)
- A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer (2012) (185)
- A susceptibility gene for psoriatic arthritis maps to chromosome 16q: evidence for imprinting. (2003) (180)
- Covariance Structure and Convergence Rate of the Gibbs Sampler with Various Scans (1995) (176)
- A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer (2010) (174)
- Expanding the range of ZNF804A variants conferring risk of psychosis (2011) (169)
- The Association of a SNP Upstream of INSIG2 with Body Mass Index is Reproduced in Several but Not All Cohorts (2007) (163)
- Weighting sequence variants based on their annotation increases power of whole-genome association studies (2016) (159)
- Blocking Gibbs sampling in very large probabilistic expert systems (1995) (158)
- Genetic Correction of PSA Values Using Sequence Variants Associated with PSA Levels (2010) (154)
- Graphical Templates for Model Registration (1996) (151)
- Identification of low-frequency variants associated with gout and serum uric acid levels (2011) (149)
- A genome-wide scan for preeclampsia in the Netherlands (2001) (147)
- Physical and neurobehavioral determinants of reproductive onset and success (2016) (146)
- The genetic spectrum of a population-based sample of familial hemiplegic migraine. (2007) (139)
- A sequence variant on 17q21 is associated with age at onset and severity of asthma (2010) (137)
- A major susceptibility gene for asthma maps to chromosome 14q24. (2002) (133)
- European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene. (2011) (133)
- Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases (2010) (131)
- A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration (2013) (129)
- Selection against variants in the genome associated with educational attainment (2017) (129)
- A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration). (2004) (127)
- Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31 (2014) (125)
- Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits (2008) (122)
- Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption. (2011) (121)
- Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms (2014) (120)
- Relatedness disequilibrium regression estimates heritability without environmental bias (2018) (119)
- Familial risk of lung carcinoma in the Icelandic population. (2004) (118)
- Male-pattern baldness susceptibility locus at 20p11 (2008) (117)
- HLA class II sequence variants influence tuberculosis risk in populations of European ancestry (2016) (117)
- Genetic Architecture of Vitamin B12 and Folate Levels Uncovered Applying Deeply Sequenced Large Datasets (2013) (115)
- Deconstructing the sources of genotype-phenotype associations in humans (2019) (108)
- Common and low-frequency variants associated with genome-wide recombination rate (2013) (106)
- Linkage of Essential Hypertension to Chromosome 18q (2002) (105)
- The Impact of Divergence Time on the Nature of Population Structure: An Example from Iceland (2009) (103)
- A theory of statistical models for Monte Carlo integration (2003) (101)
- Common variant at 16p11.2 conferring risk of psychosis (2014) (100)
- Multi-nucleotide de novo Mutations in Humans (2016) (97)
- Localization of a gene for migraine without aura to chromosome 4q21. (2003) (97)
- Anxiety with panic disorder linked to chromosome 9q in Iceland. (2003) (96)
- Allelic frequencies and patterns of single-nucleotide polymorphisms in candidate genes for asthma and atopy in Iceland. (2001) (92)
- Whole genome characterization of sequence diversity of 15,220 Icelanders (2017) (90)
- Finding the missing heritability of complex (2009) (87)
- The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms (2014) (87)
- Blocking Gibbs sampling for linkage analysis in large pedigrees with many loops. (1999) (83)
- Multiple transmissions of de novo mutations in families (2018) (81)
- The Y-chromosome point mutation rate in humans (2015) (81)
- European Bone Mineral Density Loci Are Also Associated with BMD in East-Asian Populations (2010) (80)
- Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis (2017) (75)
- The BARD1 Cys557Ser Variant and Breast Cancer Risk in Iceland (2006) (75)
- The rate of meiotic gene conversion varies by sex and age (2016) (72)
- A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation (2017) (72)
- Sequence variants from whole genome sequencing a large group of Icelanders (2015) (67)
- Localization of a gene for peripheral arterial occlusive disease to chromosome 1p31. (2002) (66)
- Truncating mutations in RBM12 are associated with psychosis (2017) (65)
- Correction: Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases (2010) (64)
- A common variant at 8q24.21 is associated with renal cell cancer (2013) (62)
- Familial predisposition and cosegregation analysis of adult obstructive sleep apnea and the sudden infant death syndrome. (2002) (61)
- Corrigendum: Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes (2011) (60)
- Sequential imputation for multilocus linkage analysis. (1994) (60)
- New basal cell carcinoma susceptibility loci (2015) (58)
- Unsupervised empirical Bayesian multiple testing with external covariates (2008) (56)
- Epigenetic and genetic components of height regulation (2016) (49)
- Rare mutations associating with serum creatinine and chronic kidney disease. (2014) (48)
- Support for involvement of the AHI1 locus in schizophrenia (2007) (46)
- Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma (2014) (42)
- Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer. (2014) (41)
- Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution (2009) (39)
- The genealogic approach to human genetics of disease. (2001) (38)
- The role of linkage studies for common diseases. (2001) (35)
- Linkage mapping in experimental crosses: the robustness of single-gene models. (1997) (35)
- Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation (2017) (31)
- CDKN2A mutations and melanoma risk in the Icelandic population (2008) (31)
- Mendelian imputation of parental genotypes for genome-wide estimation of direct and indirect genetic effects (2020) (30)
- Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk. (2011) (25)
- Asymptotic theory for gene mapping. (1994) (24)
- Reproductive fitness and genetic risk of psychiatric disorders in the general population (2017) (23)
- A systematic evaluation of 151 candidate genes for their association with osteoporosis and osteoporotic fracture in a meta-analysis of genome-wide association data (2009) (22)
- Efficient methods for computing linkage likelihoods of recessive diseases in inbred pedigrees (1991) (21)
- Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116)) (2010) (20)
- Sequential imputation and multipoint linkage analysis (1993) (20)
- Insertion of an SVA-E retrotransposon into the CASP8 gene is associated with protection against prostate cancer (2016) (18)
- [Probabilistic Expert Systems in Medicine: Practical Issues in Handling Uncertainty]: Comment (1987) (16)
- Reconstructing an African haploid genome from the 18th century (2018) (15)
- Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2011) (15)
- Importance sampling. I. Computing multimodel p values in linkage analysis. (1992) (15)
- Rejoinder: Quantifying the Fraction of Missing Information for Hypothesis Testing in Statistical and Genetic Studies (2008) (15)
- Measuring the Relative Information in Allele‐Sharing Linkage Studies (2004) (15)
- Family Analysis with Mendelian Imputations (2020) (13)
- Optimality Issues in Constructing a Markov Tree from Graphical Models (2006) (12)
- Sequence variants at CYP 1 A 1 – CYP 1 A 2 and AHR associate with coffee consumption (2011) (11)
- Linkage analysis with adjustment for covariates: a method combining peeling with Gibbs sampling. (1992) (10)
- Erratum: Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes (Nature Genetics (2011) 43 (561-564)) (2011) (9)
- Twenty loci associated with bone mineral density identified by large-scale meta-analysis of genome-wide association datasets (2009) (8)
- Diabetes, dependence, asymptotics, selection and significance (1997) (8)
- Corrigendum: The gene encoding phosphodiesterase 4D confers risk of ischemic stroke (2005) (8)
- Mutations in BRIP 1 / FANCJ confer high risk of ovarian cancer (2015) (7)
- Genome-wide association study yields variants at 20 p 12 . 2 that associate with urinary bladder cancer (2014) (7)
- On a randomization procedure. (2000) (6)
- Reply to “Many hypotheses but no replication for the association between PDE4D and stroke” (2006) (6)
- The Genetics of Participation: Method and Analysis (2022) (6)
- FURTHER EXPLORATIONS OF LIKELIHOOD THEORY FOR MONTE CARLO INTEGRATION (2007) (6)
- Estimating heritability without environmental bias (2017) (5)
- A common variant at 8 q 24 . 21 is associated with renal cell cancer (2017) (4)
- Comment on the phosphodiesterase 4D replication study by Bevan et al. (2005) (4)
- Corrigendum: ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma (2008) (4)
- The properties of the cross-match estimate and split sampling (1997) (4)
- Sequence variant at 8 q 24 . 21 associates with sciatica caused by lumbar disc herniation (2017) (3)
- Augustine Kong Recombination Rate Gene Associate with Genome-Wide RNF 212 Sequence Variants in the (3)
- Reply to “A call for accurate phenotype definition in the study of complex disorders” (2004) (3)
- Genealogy certainly matters for multifactorial genetic disease (1999) (2)
- Whole genome sequencing finds rare high-risk genotypes for hip osteoarthritis in the COMP and CHADL genes (2017) (2)
- Recurrence of de novo mutations in families (2017) (2)
- Author Correction: The rate of meiotic gene conversion varies by sex and age (2018) (1)
- Corrigendum: Variant in the sequence of the LINGO1 gene confers risk of essential tremor (2009) (1)
- Abstract 2318: The Type 2 Diabetes Gene CDKAL1 Discovered by Genome-wide Association is Expressed in Beta Cells and Modulated by Glucose Concentration (2007) (1)
- Abstract PR-7: A European genome-wide association study of urinary bladder cancer (2008) (0)
- Multiple transmissions of de novo mutations in families (2018) (0)
- Errata (2011) (0)
- HAPMIX results of chromosome 6 in chiptyped Icelanders (2017) (0)
- Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis. (2017) (0)
- Reconstructing an African haploid genome from the 18th century (2018) (0)
- Title European bone mineral density loci are also associated withBMD in East-Asian populations (2010) (0)
- A sequence variant associating with educational attainment also affects childhood cognition (2016) (0)
- Importance Sampling. 1.Computing Multimodel p Values inLinkage Analysis (1992) (0)
- Author Correction: The rate of meiotic gene conversion varies by sex and age (2018) (0)
- Erratum to “Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis” (2000) (0)
- Recombination Rate : A Hidden Phenotype (2005) (0)
- Severe osteoarthritis of the hand associates with markers within the ALDH1A2 gene and with very rare variants at 1p31 (2017) (0)
- Abstract 2921: Genome-wide Association Reveals Sequence Variants on 4q25 that Affect the Risk of Atrial Fibrillation and Stroke (2007) (0)
- Contributors and Participants (1982) (0)
- 133 Evidence of heritability of the common form of atrial fibrillation (2005) (0)
- Relatedness disequilibrium regression estimates heritability without environmental bias (2018) (0)
- Computing Multimodel p Values in Linkage Analysis (2006) (0)
- Rejoinder: Quantifying the Fraction of Missing Information for Hypothesis Testing in Statistical and Genetic Studies (2011) (0)
- Abstract 1964: A Genome-Wide Association Study in Icelanders Identifies a Novel Sequence Variant on Chromosome 16q22 That is Additive to 4q25 Variants for Atrial Fibrillation Risk (2009) (0)
- Genetic factors contributing to the risk of endometriosis: data from a population-based study (2002) (0)
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