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Harald H. Goring, Ph.D. - Publications

Affiliations: 
2000 Columbia University, New York, NY 
Area:
Genetics, Statistics, Biostatistics Biology
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33 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Sanders A, Duan J, Drigalenko E, Goring H, Gejman P. RNAseq TRANSCRIPTOME STUDY OF SCHIZOPHRENIA IN THE MGS AFRICAN AMERICAN SAMPLE European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.170  0.37
2017 Knowles EE, Meikle PJ, Huynh K, Göring HH, Olvera RL, Mathias SR, Duggirala R, Almasy L, Blangero J, Curran JE, Glahn DC. Serum phosphatidylinositol as a biomarker for bipolar disorder liability. Bipolar Disorders. PMID 28230325 DOI: 10.1016/J.Euroneuro.2016.09.521  0.301
2017 Knowles E, Curran J, Meikle P, Huynh K, Goring H, Olvera R, Duggirala R, Almasy L, Blangero J, Glahn D. Disentangling The Shared Genetic Etiology Between Serum Cholesterol And Suicide Risk: A Potential Moderating Role For Cholesterol Efflux European Neuropsychopharmacology. 27. DOI: 10.1016/J.Euroneuro.2016.09.588  0.333
2017 Curran J, Knowles E, Huynh K, Meikle P, Goring H, Olvera R, Mathias S, Duggirala R, Almasy L, Blangero J, Glahn D. The Lipidome In Major Depressive Disorder: Shared Genetic Influence For Ether-Phosphatidylcholines, A Plasma-Based Phenotype Related To Inflammation, And Disease Risk European Neuropsychopharmacology. 27. DOI: 10.1016/J.Euroneuro.2016.09.500  0.33
2017 Mathias S, Knowles E, Curran J, Goring H, Olvera R, Fox P, Duggirala R, Almasy L, Blangero J, Glahn D. An Exploratory Study of The Genetic Relationships Between Plasma-Based Measures of Inflammation And Brain Anatomy European Neuropsychopharmacology. 27. DOI: 10.1016/J.Euroneuro.2016.09.409  0.355
2016 Kulkarni H, Mamtani M, Peralta JM, Diego V, Dyer TD, Goring H, Almasy L, Mahaney MC, Williams-Blangero S, Duggirala R, Curran JE, Blangero J. Lack of Association between SLC30A8 Variants and Type 2 Diabetes in Mexican American Families. Journal of Diabetes Research. 2016: 6463214. PMID 27896278 DOI: 10.1155/2016/6463214  0.368
2016 Hodgson K, Almasy L, Knowles EE, Kent JW, Curran JE, Dyer TD, Göring HH, Olvera RL, Woolsey MD, Duggirala R, Fox PT, Blangero J, Glahn DC. The genetic basis of the comorbidity between cannabis use and major depression. Addiction (Abingdon, England). PMID 27517884 DOI: 10.1111/add.13558  0.303
2016 Jenkinson CP, Göring HH, Arya R, Blangero J, Duggirala R, DeFronzo RA. Transcriptomics in type 2 diabetes: Bridging the gap between genotype and phenotype. Genomics Data. 8: 25-36. PMID 27114903 DOI: 10.1016/J.Gdata.2015.12.001  0.344
2015 Traurig M, Hanson RL, Marinelarena A, Kobes S, Piaggi P, Cole S, Curran JE, Blangero J, Göring H, Kumar S, Nelson RG, Howard BV, Knowler WC, Baier LJ, Bogardus C. Analysis of SLC16A11 variants in 12,811 American Indians: genotype-obesity interaction for type 2 diabetes and an association with RNASEK expression. Diabetes. PMID 26487785 DOI: 10.2337/Db15-0571  0.3
2015 Mathias SR, Knowles EE, Kent JW, McKay DR, Curran JE, de Almeida MA, Dyer TD, Göring HH, Olvera RL, Duggirala R, Fox PT, Almasy L, Blangero J, Glahn DC. Recurrent major depression and right hippocampal volume: A bivariate linkage and association study. Human Brain Mapping. PMID 26485182 DOI: 10.1002/Hbm.23025  0.373
2015 Benton MC, Lea RA, Macartney-Coxson D, Hanna M, Eccles DA, Carless MA, Chambers GK, Bellis C, Goring HH, Curran JE, Harper JL, Gibson G, Blangero J, Griffiths LR. A Phenomic Scan of the Norfolk Island Genetic Isolate Identifies a Major Pleiotropic Effect Locus Associated with Metabolic and Renal Disorder Markers. Plos Genetics. 11: e1005593. PMID 26474483 DOI: 10.1371/Journal.Pgen.1005593  0.419
2015 Rodriguez-Acevedo AJ, Ferreira MA, Benton MC, Carless MA, Goring HH, Curran JE, Blangero J, Lea RA, Griffiths LR. Common polygenic variation contributes to risk of migraine in the Norfolk Island population Human Genetics. 134: 1079-1087. PMID 26220684 DOI: 10.1007/S00439-015-1587-9  0.405
2015 Dager AD, McKay DR, Kent JW, Curran JE, Knowles E, Sprooten E, Göring HH, Dyer TD, Pearlson GD, Olvera RL, Fox PT, Lovallo WR, Duggirala R, Almasy L, Blangero J, et al. Shared genetic factors influence amygdala volumes and risk for alcoholism. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 40: 412-20. PMID 25079289 DOI: 10.1038/Npp.2014.187  0.333
2014 Quillen EE, Voruganti VS, Chittoor G, Rubicz R, Peralta JM, Almeida MA, Kent JW, Diego VP, Dyer TD, Comuzzie AG, Göring HH, Duggirala R, Almasy L, Blangero J. Evaluation of estimated genetic values and their application to genome-wide investigation of systolic blood pressure. Bmc Proceedings. 8: S66. PMID 25519398 DOI: 10.1186/1753-6561-8-S1-S66  0.327
2014 Franceschini N, Tao R, Liu L, Rutherford S, Haack K, Almasy L, Göring HH, Laston S, Lee ET, Best LG, Fabsitz R, Cole SA, North KE. Mapping of a blood pressure QTL on chromosome 17 in American Indians of the strong heart family study. Bmc Cardiovascular Disorders. 14: 158. PMID 25387527 DOI: 10.1186/1471-2261-14-158  0.392
2013 Voruganti VS, Kent JW, Debnath S, Cole SA, Haack K, Göring HH, Carless MA, Curran JE, Johnson MP, Almasy L, Dyer TD, Maccluer JW, Moses EK, Abboud HE, Mahaney MC, et al. Genome-wide association analysis confirms and extends the association of SLC2A9 with serum uric acid levels to Mexican Americans. Frontiers in Genetics. 4: 279. PMID 24379826 DOI: 10.3389/Fgene.2013.00279  0.392
2013 Kochunov P, Charlesworth J, Winkler A, Hong LE, Nichols TE, Curran JE, Sprooten E, Jahanshad N, Thompson PM, Johnson MP, Kent JW, Landman BA, Mitchell B, Cole SA, Dyer TD, ... ... Goring HH, et al. Transcriptomics of cortical gray matter thickness decline during normal aging. Neuroimage. 82: 273-83. PMID 23707588 DOI: 10.1016/J.Neuroimage.2013.05.066  0.332
2012 Bella JN, Göring HH. Genetic epidemiology of left ventricular hypertrophy. American Journal of Cardiovascular Disease. 2: 267-78. PMID 23173100  0.327
2012 Kochunov P, Glahn DC, Hong LE, Lancaster J, Curran JE, Johnson MP, Winkler AM, Holcomb HH, Kent JW, Mitchell B, Kochunov V, Olvera RL, Cole SA, Dyer TD, Moses EK, ... Goring H, et al. P-selectin Expression Tracks Cerebral Atrophy in Mexican-Americans. Frontiers in Genetics. 3: 65. PMID 22558002 DOI: 10.3389/Fgene.2012.00065  0.333
2012 Hiekkalinna T, Göring HH, Terwilliger JD. On the validity of the likelihood ratio test and consistency of resulting parameter estimates in joint linkage and linkage disequilibrium analysis under improperly specified parametric models. Annals of Human Genetics. 76: 63-73. PMID 22082140 DOI: 10.1111/J.1469-1809.2011.00683.X  0.533
2011 Kent JW, Farook V, Göring HH, Dyer TD, Almasy L, Duggirala R, Blangero J. Do rare variant genotypes predict common variant genotypes? Bmc Proceedings. 5: S87. PMID 22373504 DOI: 10.1186/1753-6561-5-S9-S87  0.318
2011 Hiekkalinna T, Schäffer AA, Lambert B, Norrgrann P, Göring HH, Terwilliger JD. PSEUDOMARKER: a powerful program for joint linkage and/or linkage disequilibrium analysis on mixtures of singletons and related individuals. Human Heredity. 71: 256-66. PMID 21811076 DOI: 10.1159/000329467  0.581
2011 Melton PE, Haack K, Göring HH, Laston S, Umans JG, Lee ET, Fabsitz RR, Devereux RB, Best LG, Maccluer JW, Almasy L, Cole SA. Genetic influences on serum bilirubin in American Indians: The Strong Heart Family Study. American Journal of Human Biology : the Official Journal of the Human Biology Council. 23: 118-25. PMID 21080475 DOI: 10.1002/Ajhb.21114  0.394
2009 Terwilliger JD, Göring HH. Update to Terwilliger and Göring's "Gene mapping in the 20th and 21st centuries" (2000): gene mapping when rare variants are common and common variants are rare. Human Biology. 81: 729-33. PMID 20504192 DOI: 10.3378/027.081.0617  0.56
2009 Terwilliger JD, Göring HH. Gene mapping in the 20th and 21st centuries: statistical methods, data analysis, and experimental design. 2000. Human Biology. 81: 663-728. PMID 20504191 DOI: 10.3378/027.081.0615  0.581
2009 Charlesworth JC, Peralta JM, Drigalenko E, Göring HH, Almasy L, Dyer TD, Blangero J. Toward the identification of causal genes in complex diseases: a gene-centric joint test of significance combining genomic and transcriptomic data. Bmc Proceedings. 3: S92. PMID 20018089 DOI: 10.1186/1753-6561-3-S7-S92  0.368
2008 Best LG, North KE, Li X, Palmieri V, Umans JG, MacCluer J, Laston S, Haack K, Goring H, Diego VP, Almasy L, Lee ET, Tracy RP, Cole S. Linkage study of fibrinogen levels: the Strong Heart Family Study. Bmc Medical Genetics. 9: 77. PMID 18700015 DOI: 10.1186/1471-2350-9-77  0.399
2008 Pulli K, Karma K, Norio R, Sistonen P, Göring HH, Järvelä IE. Genome-wide linkage scan for loci of musical aptitude in Finnish families: evidence for a major locus at 4q22 Journal of Medical Genetics. 45: 451-456. PMID 18424507 DOI: 10.1136/Jmg.2007.056366  0.378
2007 Kent JW, Mahaney MC, Comuzzie AG, Göring HH, Almasy L, Dyer TD, Cole SA, MacCluer JW, Blangero J. Quantitative trait locus on Chromosome 19 for circulating levels of intercellular adhesion molecule-1 in Mexican Americans. Atherosclerosis. 195: 367-73. PMID 17112530 DOI: 10.1016/J.Atherosclerosis.2006.10.005  0.306
2006 Cai G, Cole SA, Butte N, Bacino C, Diego V, Tan K, Göring HH, O'Rahilly S, Farooqi IS, Comuzzie AG. A quantitative trait locus on chromosome 18q for physical activity and dietary intake in Hispanic children. Obesity (Silver Spring, Md.). 14: 1596-604. PMID 17030971 DOI: 10.1038/Oby.2006.184  0.301
2005 Blangero J, Goring HH, Kent JW, Williams JT, Peterson CP, Almasy L, Dyer TD. Quantitative trait nucleotide analysis using Bayesian model selection. Human Biology. 77: 541-59. PMID 16596940 DOI: 10.1353/Hub.2006.0003  0.341
2004 Samollow PB, Perez G, Kammerer CM, Finegold D, Zwartjes PW, Havill LM, Comuzzie AG, Mahaney MC, Göring HH, Blangero J, Foley TP, Barmada MM. Genetic and environmental influences on thyroid hormone variation in Mexican Americans. The Journal of Clinical Endocrinology and Metabolism. 89: 3276-84. PMID 15240603 DOI: 10.1210/Jc.2003-031706  0.315
2002 Terwilliger JD, Haghighi F, Hiekkalinna TS, Göring HH. A bias-ed assessment of the use of SNPs in human complex traits. Current Opinion in Genetics & Development. 12: 726-34. PMID 12433588 DOI: 10.1016/S0959-437X(02)00357-X  0.583
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