| Year |
Citation |
Score |
| 2016 |
Magnus P, Sinsheimer JS, Clark MM, Chazara O, Sobel EM, Gjessing HK, Moffett A, Hodge SE, Greenberg DA, Kim W, Gordon D, Londono D, Patel P, Finch SJ, Heiman GA, et al. 45th European Mathematical Genetics Meeting (EMGM) 2017, Tartu, Estonia, April 4-7, 2017: Abstracts Human Heredity. 81: 211-238. PMID 28376496 DOI: 10.1159/000469638 |
0.301 |
|
| 2013 |
Helbig I, Hodge SE, Ottman R. Familial cosegregation of rare genetic variants with disease in complex disorders. European Journal of Human Genetics : Ejhg. 21: 444-50. PMID 23010752 DOI: 10.1038/Ejhg.2012.194 |
0.41 |
|
| 2012 |
Subaran RL, Talati A, Hamilton SP, Adams P, Weissman MM, Fyer AJ, Hodge SE. A survey of putative anxiety-associated genes in panic disorder patients with and without bladder symptoms. Psychiatric Genetics. 22: 271-8. PMID 23018769 DOI: 10.1097/Ypg.0B013E3283586248 |
0.379 |
|
| 2012 |
Fyer AJ, Costa R, Haghighi F, Logue MW, Knowles JA, Weissman MM, Hodge SE, Hamilton SP. Linkage analysis of alternative anxiety phenotypes in multiply affected panic disorder families. Psychiatric Genetics. 22: 123-9. PMID 22525237 DOI: 10.1097/Ypg.0B013E328353956A |
0.676 |
|
| 2011 |
Hodge SE, Baskurt Z, Strug LJ. Using parametric multipoint lods and mods for linkage analysis requires a shift in statistical thinking. Human Heredity. 72: 264-75. PMID 22189469 DOI: 10.1159/000331463 |
0.378 |
|
| 2011 |
Madsen AM, Ottman R, Hodge SE. Causal models for investigating complex genetic disease: II. what causal models can tell us about penetrance for additive, heterogeneity, and multiplicative two-locus models. Human Heredity. 72: 63-72. PMID 21912139 DOI: 10.1159/000330780 |
0.347 |
|
| 2011 |
Madsen AM, Hodge SE, Ottman R. Causal models for investigating complex disease: I. A primer. Human Heredity. 72: 54-62. PMID 21912138 DOI: 10.1159/000330779 |
0.364 |
|
| 2010 |
Strug LJ, Hodge SE, Chiang T, Pal DK, Corey PN, Rohde C. A pure likelihood approach to the analysis of genetic association data: an alternative to Bayesian and frequentist analysis. European Journal of Human Genetics : Ejhg. 18: 933-41. PMID 20424645 DOI: 10.1038/Ejhg.2010.47 |
0.343 |
|
| 2010 |
Gorroochurn P, Hodge SE, Heiman GA, Greenberg DA. Comments on 'Delta-centralization fails to control for population stratification in genetic association studies'. Human Heredity. 69: 295. PMID 20389098 DOI: 10.1159/000298766 |
0.316 |
|
| 2010 |
Greenberg DA, Monti MC, Feenstra B, Zhang J, Hodge SE. The essence of linkage-based imprinting detection: comparing power, type 1 error, and the effects of confounders in two different analysis approaches. Annals of Human Genetics. 74: 248-62. PMID 20374235 DOI: 10.1111/J.1469-1809.2010.00568.X |
0.301 |
|
| 2010 |
Gyawali S, Subaran R, Weissman MM, Hershkowitz D, McKenna MC, Talati A, Fyer AJ, Wickramaratne P, Adams PB, Hodge SE, Schmidt CJ, Bannon MJ, Glatt CE. Association of a polyadenylation polymorphism in the serotonin transporter and panic disorder. Biological Psychiatry. 67: 331-8. PMID 19969287 DOI: 10.1016/J.Biopsych.2009.10.015 |
0.338 |
|
| 2010 |
Strug LJ, Suresh R, Fyer AJ, Talati A, Adams PB, Li W, Hodge SE, Gilliam TC, Weissman MM. Panic disorder is associated with the serotonin transporter gene (SLC6A4) but not the promoter region (5-HTTLPR). Molecular Psychiatry. 15: 166-76. PMID 18663369 DOI: 10.1038/Mp.2008.79 |
0.369 |
|
| 2009 |
Petukhova L, Shimomura Y, Wajid M, Gorroochurn P, Hodge SE, Christiano AM. The effect of inbreeding on the distribution of compound heterozygotes: a lesson from Lipase H mutations in autosomal recessive woolly hair/hypotrichosis. Human Heredity. 68: 117-30. PMID 19365138 DOI: 10.1159/000212504 |
0.378 |
|
| 2009 |
Logue MW, Durner M, Heiman GA, Hodge SE, Hamilton SP, Knowles JA, Fyer AJ, Weissman MM. A linkage search for joint panic disorder/bipolar genes. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 1139-46. PMID 19308964 DOI: 10.1002/Ajmg.B.30939 |
0.363 |
|
| 2009 |
Mann JJ, Arango VA, Avenevoli S, Brent DA, Champagne FA, Clayton P, Currier D, Dougherty DM, Haghighi F, Hodge SE, Kleinman J, Lehner T, McMahon F, Mo?cicki EK, Oquendo MA, et al. Candidate endophenotypes for genetic studies of suicidal behavior. Biological Psychiatry. 65: 556-63. PMID 19201395 DOI: 10.1016/J.Biopsych.2008.11.021 |
0.311 |
|
| 2008 |
Hodge SE, Rodriguez-Murillo L, Strug LJ, Greenberg DA. Multipoint lods provide reliable linkage evidence despite unknown limiting distribution: type I error probabilities decrease with sample size for multipoint lods and mods. Genetic Epidemiology. 32: 800-15. PMID 18613118 DOI: 10.1002/Gepi.20350 |
0.32 |
|
| 2008 |
Talati A, Ponniah K, Strug LJ, Hodge SE, Fyer AJ, Weissman MM. Panic disorder, social anxiety disorder, and a possible medical syndrome previously linked to chromosome 13. Biological Psychiatry. 63: 594-601. PMID 17920564 DOI: 10.1016/J.Biopsych.2007.07.021 |
0.359 |
|
| 2007 |
Gorroochurn P, Hodge SE, Heiman GA, Greenberg DA. A unified approach for quantifying, testing and correcting population stratification in case-control association studies. Human Heredity. 64: 149-59. PMID 17536209 DOI: 10.1159/000102988 |
0.312 |
|
| 2006 |
Fyer AJ, Hamilton SP, Durner M, Haghighi F, Heiman GA, Costa R, Evgrafov O, Adams P, de Leon AB, Taveras N, Klein DF, Hodge SE, Weissman MM, Knowles JA. A third-pass genome scan in panic disorder: evidence for multiple susceptibility loci. Biological Psychiatry. 60: 388-401. PMID 16919526 DOI: 10.1016/J.Biopsych.2006.04.018 |
0.647 |
|
| 2006 |
Strug LJ, Hodge SE. An alternative foundation for the planning and evaluation of linkage analysis. II. Implications for multiple test adjustments. Human Heredity. 61: 200-9. PMID 16877867 DOI: 10.1159/000094775 |
0.317 |
|
| 2006 |
Strug LJ, Hodge SE. An alternative foundation for the planning and evaluation of linkage analysis. I. Decoupling "error probabilities" from "measures of evidence". Human Heredity. 61: 166-88. PMID 16865000 DOI: 10.1159/000094709 |
0.389 |
|
| 2006 |
Hodge SE, Ban Y, Strug LJ, Greenberg DA, Davies TF, Concepcion ES, Villanueva R, Tomer Y. Possible interaction between HLA-DRbeta1 and thyroglobulin variants in Graves' disease. Thyroid : Official Journal of the American Thyroid Association. 16: 351-5. PMID 16646680 DOI: 10.1089/Thy.2006.16.351 |
0.328 |
|
| 2006 |
Gorroochurn P, Heiman GA, Hodge SE, Greenberg DA. Centralizing the non-central chi-square: A new method to correct for population stratification in genetic case-control association studies. Genetic Epidemiology. 30: 277-89. PMID 16502404 DOI: 10.1002/Gepi.20143 |
0.301 |
|
| 2005 |
Tsai WY, Heiman GA, Hodge SE. New simple tests for age-at-onset anticipation: application to panic disorder. Genetic Epidemiology. 28: 256-60. PMID 15637720 DOI: 10.1002/Gepi.20057 |
0.326 |
|
| 2004 |
Lindholm E, Hodge SE, Greenberg DA. Comparative informativeness for linkage of multiple SNPs and single microsatellites Human Heredity. 58: 164-170. PMID 15812173 DOI: 10.1159/000083543 |
0.373 |
|
| 2004 |
Heiman GA, Hodge SE, Gorroochurn P, Zhang J, Greenberg DA. Effect of population stratification on case-control association studies. I. Elevation in false positive rates and comparison to confounding risk ratios (a simulation study). Human Heredity. 58: 30-9. PMID 15604562 DOI: 10.1159/000081454 |
0.32 |
|
| 2004 |
Lindholm E, Zhang J, Hodge SE, Greenberg DA. The reliability of haplotyping inference in nuclear families: Misassignment rates for SNPs and microsatellites Human Heredity. 57: 117-127. PMID 15297805 DOI: 10.1159/000079242 |
0.34 |
|
| 2004 |
Hamilton SP, Slager SL, Mayo D, Heiman GA, Klein DF, Hodge SE, Fyer AJ, Weissman MM, Knowles JA. Investigation of polymorphisms in the CREM gene in panic disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 126: 111-5. PMID 15048659 DOI: 10.1002/Ajmg.B.20121 |
0.469 |
|
| 2004 |
Weissman MM, Gross R, Fyer A, Heiman GA, Gameroff MJ, Hodge SE, Kaufman D, Kaplan SA, Wickramaratne PJ. Interstitial cystitis and panic disorder: a potential genetic syndrome. Archives of General Psychiatry. 61: 273-9. PMID 14993115 DOI: 10.1001/Archpsyc.61.3.273 |
0.39 |
|
| 2004 |
Hamilton SP, Slager SL, De Leon AB, Heiman GA, Klein DF, Hodge SE, Weissman MM, Fyer AJ, Knowles JA. Evidence for genetic linkage between a polymorphism in the adenosine 2A receptor and panic disorder. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 29: 558-65. PMID 14666117 DOI: 10.1038/Sj.Npp.1300311 |
0.428 |
|
| 2003 |
Flodman P, Hodge SE. Sex-specific mutation rates for x-linked disorders: estimation and application. Human Heredity. 55: 51-5. PMID 12890926 DOI: 10.1159/000071810 |
0.309 |
|
| 2003 |
Hamilton SP, Fyer AJ, Durner M, Heiman GA, Baisre de Leon A, Hodge SE, Knowles JA, Weissman MM. Further genetic evidence for a panic disorder syndrome mapping to chromosome 13q. Proceedings of the National Academy of Sciences of the United States of America. 100: 2550-5. PMID 12604791 DOI: 10.1073/Pnas.0335669100 |
0.397 |
|
| 2002 |
Flodman P, Hodge SE. Determining Complex Genetic Risks by Computer. Journal of Genetic Counseling. 11: 213-30. PMID 26141858 DOI: 10.1023/A:1015231207178 |
0.316 |
|
| 2002 |
Ahsan H, Hodge SE, Heiman GA, Begg MD, Susser ES. Relative risk for genetic associations: the case-parent triad as a variant of case-cohort design. International Journal of Epidemiology. 31: 669-78. PMID 12055172 DOI: 10.1093/Ije/31.3.669 |
0.306 |
|
| 2002 |
Slager SL, Carleu L, Chung WK, Jackson T, Winchester RJ, Hodge SE, Gulko PS. The IDDM13 region containing the insulin-like growth factor binding protein-5 (IGFBP5) gene on chromosome 2q33-q36 and the genetic susceptibility to rheumatoid arthritis. Genes and Immunity. 3: 110-3. PMID 11960310 DOI: 10.1038/Sj.Gene.6363847 |
0.34 |
|
| 2002 |
Hamilton SP, Slager SL, Heiman GA, Deng Z, Haghighi F, Klein DF, Hodge SE, Weissman MM, Fyer AJ, Knowles JA. Evidence for a susceptibility locus for panic disorder near the catechol-O-methyltransferase gene on chromosome 22. Biological Psychiatry. 51: 591-601. PMID 11950461 DOI: 10.1016/S0006-3223(01)01322-1 |
0.654 |
|
| 2002 |
Brown LY, Hodge SE, Johnson WG, Guy SG, Nye JS, Brown S. Possible association of NTDs with a polyhistidine tract polymorphism in the ZIC2 gene. American Journal of Medical Genetics. 108: 128-31. PMID 11857562 DOI: 10.1002/Ajmg.10221 |
0.312 |
|
| 2002 |
Hodge SE, Vieland VJ, Greenberg DA. HLODs remain powerful tools for detection of linkage in the presence of genetic heterogeneity. American Journal of Human Genetics. 70: 556-9. PMID 11791217 DOI: 10.1086/338923 |
0.357 |
|
| 2002 |
Abreu PC, Hodge SE, Greenberg DA. Quantification of type I error probabilities for heterogeneity LOD scores. Genetic Epidemiology. 22: 156-69. PMID 11788961 DOI: 10.1002/Gepi.0155 |
0.389 |
|
| 2002 |
Haghighi F, Hodge SE. Likelihood formulation of parent-of-origin effects on segregation analysis, including ascertainment. American Journal of Human Genetics. 70: 142-56. PMID 11741195 DOI: 10.1086/324709 |
0.586 |
|
| 2002 |
Hodge SE, Greenberg DA, Betancur C, Gillberg C. Response to Visscher American Journal of Human Genetics. 71: 996-999. DOI: 10.1086/342992 |
0.302 |
|
| 2001 |
Greenberg DA, Hodge SE, Sowinski J, Nicoll D. Excess of Twins among Affected Sibling Pairs with Autism: Implications for the Etiology of Autism American Journal of Human Genetics. 69: 1062-1067. PMID 11590546 DOI: 10.1086/324191 |
0.408 |
|
| 2001 |
Flodman P, Hodge SE. A genetic risk calculation surprise. American Journal of Medical Genetics. 100: 169-171. PMID 11298381 DOI: 10.1002/1096-8628(20010422)100:2<169::Aid-Ajmg1243>3.0.Co;2-K |
0.308 |
|
| 2001 |
Slager SL, Foroud T, Haghighi F, Spence MA, Hodge SE. Stoppage: an issue for segregation analysis. Genetic Epidemiology. 20: 328-339. PMID 11255242 DOI: 10.1002/Gepi.4 |
0.633 |
|
| 2001 |
Hamilton SP, Slager SL, Helleby L, Heiman GA, Klein DF, Hodge SE, Weissman MM, Fyer AJ, Knowles JA. No association or linkage between polymorphisms in the genes encoding cholecystokinin and the cholecystokinin B receptor and panic disorder. Molecular Psychiatry. 6: 59-65. PMID 11244486 DOI: 10.1038/Sj.Mp.4000788 |
0.448 |
|
| 2001 |
Wickramaratne PJ, Hodge SE, Guo SW. Estimation of sibling recurrence-risk ratio under single ascertainment in two-child families American Journal of Human Genetics. 68: 807-812. PMID 11179030 DOI: 10.1086/318784 |
0.308 |
|
| 2000 |
Spence MA, Hodge SE. The "Circular" Problems of Calculating Risk: Dealing with Consanguinity. Journal of Genetic Counseling. 9: 179-201. PMID 26141316 DOI: 10.1023/A:1009420304149 |
0.311 |
|
| 2000 |
Goedken R, Ludington E, Crowe R, Fyer AJ, Hodge SE, Knowles JA, Vieland VJ, Weissman MM. Drawbacks of GENEHUNTER for larger pedigrees: application to panic disorder. American Journal of Medical Genetics. 96: 781-3. PMID 11121181 DOI: 10.1002/1096-8628(20001204)96:6<781::Aid-Ajmg17>3.0.Co;2-J |
0.382 |
|
| 2000 |
Hamilton SP, Slager SL, Heiman GA, Haghighi F, Klein DF, Hodge SE, Weissman MM, Fyer AJ, Knowles JA. No genetic linkage or association between a functional promoter polymorphism in the monoamine oxidase-A gene and panic disorder. Molecular Psychiatry. 5: 465-6. PMID 11032378 DOI: 10.1038/Sj.Mp.4000772 |
0.648 |
|
| 2000 |
Deng Z, Morse JH, Slager SL, Cuervo N, Moore KJ, Venetos G, Kalachikov S, Cayanis E, Fischer SG, Barst RJ, Hodge SE, Knowles JA. Familial primary pulmonary hypertension (gene PPH1) is caused by mutations in the bone morphogenetic protein receptor-II gene. American Journal of Human Genetics. 67: 737-44. PMID 10903931 DOI: 10.1086/303059 |
0.343 |
|
| 2000 |
Hoh J, Hodge SE. A Measure of Phase Ambiguity in Pairs of SNPs in the Presence ofLinkage Disequi librium Human Heredity. 50: 359-364. PMID 10899754 DOI: 10.1159/000022941 |
0.312 |
|
| 2000 |
Hamilton SP, Haghighi F, Heiman GA, Klein DF, Hodge SE, Fyer AJ, Weissman MM, Knowles JA. Investigation of dopamine receptor (DRD4) and dopamine transporter (DAT) polymorphisms for genetic linkage or association to panic disorder. American Journal of Medical Genetics. 96: 324-30. PMID 10898909 DOI: 10.1002/1096-8628(20000612)96:3<324::Aid-Ajmg18>3.0.Co;2-W |
0.664 |
|
| 2000 |
Deng Z, Haghighi F, Helleby L, Vanterpool K, Horn EM, Barst RJ, Hodge SE, Morse JH, Knowles JA. Fine mapping of PPH1, a gene for familial primary pulmonary hypertension, to a 3-cM region on chromosome 2q33. American Journal of Respiratory and Critical Care Medicine. 161: 1055-9. PMID 10712363 DOI: 10.1164/Ajrccm.161.3.9906051 |
0.632 |
|
| 2000 |
Weissman MM, Fyer AJ, Haghighi F, Heiman G, Deng Z, Hen R, Hodge SE, Knowles JA. Potential panic disorder syndrome: clinical and genetic linkage evidence. American Journal of Medical Genetics. 96: 24-35. PMID 10686548 DOI: 10.1002/(Sici)1096-8628(20000207)96:1<24::Aid-Ajmg7>3.0.Co;2-E |
0.663 |
|
| 1999 |
Greenberg DA, MacCluer JW, Spence MA, Falk CT, Hodge SE. Simulated data for a complex genetic trait (problem 2 for GAW11): how the model was developed, and why. Genetic Epidemiology. 17: S449-59. PMID 10597475 DOI: 10.1002/Gepi.1370170773 |
0.393 |
|
| 1999 |
Abreu PC, Greenberg DA, Hodge SE. Direct power comparisons between simple LOD scores and NPL scores for linkage analysis in complex diseases. American Journal of Human Genetics. 65: 847-857. PMID 10441591 DOI: 10.1086/302536 |
0.352 |
|
| 1999 |
Hamilton SP, Heiman GA, Haghighi F, Mick S, Klein DF, Hodge SE, Weissman MM, Fyer AJ, Knowles JA. Lack of genetic linkage or association between a functional serotonin transporter polymorphism and panic disorder. Psychiatric Genetics. 9: 1-6. PMID 10335545 DOI: 10.1097/00041444-199903000-00001 |
0.649 |
|
| 1999 |
Haghighi F, Fyer AJ, Weissman MM, Knowles JA, Hodge SE. Parent-of-origin effect in panic disorder. American Journal of Medical Genetics. 88: 131-5. PMID 10206231 DOI: 10.1002/(Sici)1096-8628(19990416)88:2<131::Aid-Ajmg7>3.0.Co;2-L |
0.631 |
|
| 1998 |
Hodge SE. A Simple, Unified Approach to Bayesian Risk Calculations. Journal of Genetic Counseling. 7: 235-261. PMID 26141402 DOI: 10.1023/A:1022843223026 |
0.307 |
|
| 1998 |
Wickramaratne PJ, Hodge SE, Rotondo A. Association studies in the presence of comorbidity: Design and analysis American Journal of Medical Genetics - Neuropsychiatric Genetics. 81: 355-360. PMID 9754619 DOI: 10.1002/(Sici)1096-8628(19980907)81:5<355::Aid-Ajmg2>3.0.Co;2-S |
0.349 |
|
| 1998 |
Greenberg DA, Abreu P, Hodge SE. The Power to Detect Linkage in Complex Disease by Means of Simple LOD-Score Analyses American Journal of Human Genetics. 63: 870-879. PMID 9718328 DOI: 10.1086/301997 |
0.354 |
|
| 1998 |
Leder RO, Mansbridge JN, Hallmayer J, Hodge SE. Familial psoriasis and HLA-B: unambiguous support for linkage in 97 published families. Human Heredity. 48: 198-211. PMID 9694251 DOI: 10.1159/000022802 |
0.345 |
|
| 1998 |
Morse JH, Jones AC, Barst RJ, Hodge SE, Wilhelmsen KC, Nygaard TG. Familial primary pulmonary hypertension locus mapped to chromosome 2q31-q32. Chest. 114: 57S-58S. PMID 9676630 DOI: 10.1378/Chest.114.1_Supplement.57S |
0.302 |
|
| 1998 |
Knowles JA, Fyer AJ, Vieland VJ, Weissman MM, Hodge SE, Heiman GA, Haghighi F, de Jesus GM, Rassnick H, Preud'homme-Rivelli X, Austin T, Cunjak J, Mick S, Fine LD, Woodley KA, et al. Results of a genome-wide genetic screen for panic disorder. American Journal of Medical Genetics. 81: 139-47. PMID 9613853 DOI: 10.1002/(Sici)1096-8628(19980328)81:2<139::Aid-Ajmg4>3.0.Co;2-R |
0.658 |
|
| 1998 |
Wallenstein S, Hodge SE, Weston A. Logistic regression model for analyzing extended haplotype data. Genetic Epidemiology. 15: 173-181. PMID 9554554 DOI: 10.1002/(Sici)1098-2272(1998)15:2<173::Aid-Gepi5>3.0.Co;2-7 |
0.392 |
|
| 1998 |
Hodge SE. Exact elods and exact power for affected sib pairs analyzed for linkage under simple right and wrong models. American Journal of Medical Genetics. 81: 66-72. PMID 9514591 DOI: 10.1002/(Sici)1096-8628(19980207)81:1<66::Aid-Ajmg13>3.0.Co;2-U |
0.356 |
|
| 1998 |
Vieland VJ, Hodge SE. Statistical Evidence: A Likelihood Paradigm American Journal of Human Genetics. 63: 283-289. DOI: 10.1086/499065 |
0.302 |
|
| 1997 |
Morse JH, Jones AC, Barst RJ, Hodge SE, Wilhelmsen KC, Nygaard TG. Mapping of familial primary pulmonary hypertension locus (PPH1) to chromosome 2q31-q32. Circulation. 95: 2603-6. PMID 9193425 DOI: 10.1161/01.Cir.95.12.2603 |
0.381 |
|
| 1996 |
Durner M, Greenberg DA, Hodge SE. Phenocopies versus genetic heterogeneity : Can we use phenocopy frequencies in linkage analysis to compensate for heterogeneity ? Human Heredity. 46: 265-273. PMID 8854142 DOI: 10.1159/000154363 |
0.37 |
|
| 1996 |
Heiman GA, Hodge SE, Wickramaratne P, Hsu H. Age-at-interview bias in anticipation studies: Computer simulations and an example with panic disorder Psychiatric Genetics. 6: 61-66. PMID 8840391 DOI: 10.1097/00041444-199622000-00005 |
0.338 |
|
| 1996 |
Knowles J, Vieland V, Weissman M, Heiman G, de Jesus G, Judenberg A, Cunjak J, Mick S, Adams P, Hodge S, Klein D, Fyer A, Gilliam T. Panic disorder is unlikely to be a homogeneous autosomal dominant disorder: Results of a genome-wide genetic screen Biological Psychiatry. 39: 567. DOI: 10.1016/0006-3223(96)84178-3 |
0.354 |
|
| 1995 |
Hodge SE. Genetic analysis workshop 9: Development of problem 1 Genetic Epidemiology. 12: 555-560. PMID 8787972 DOI: 10.1002/Gepi.1370120605 |
0.425 |
|
| 1995 |
Hodge SE. An oliogenic disease displaying weak marker associations: a summary of contributions to problem 1 of GAW9. Genetic Epidemiology. 12: 545-554. PMID 8787971 DOI: 10.1002/Gepi.1370120604 |
0.362 |
|
| 1994 |
Hodge SE, Elston RC. Lods, wrods, and mods: The interpretation of lod scores calculated under different models Genetic Epidemiology. 11: 329-342. PMID 7813895 DOI: 10.1002/Gepi.1370110403 |
0.327 |
|
| 1994 |
Hodge SE. What association analysis can and cannot tell us about the genetics of complex disease American Journal of Medical Genetics. 54: 318-323. PMID 7726203 DOI: 10.1002/Ajmg.1320540408 |
0.379 |
|
| 1993 |
Spence MA, Bishop DT, Boehnke M, Elston RC, Falk C, Hodge SE, Ott J, Rice J, Merikangas K, Kupfer D. Methodological issues in linkage analyses for psychiatric disorders: secular trends, assortative mating, bilineal pedigrees. Report of the MacArthur Foundation Network I Task Force on Methodological Issues. Human Heredity. 43: 166-72. PMID 8330880 DOI: 10.1159/000154173 |
0.341 |
|
| 1993 |
Vieland VJ, Greenberg DA, Hodge SE. Adequacy of single-locus approximations for linkage analyses of oligogenic traits: extension to multigenerational pedigree structures. Human Heredity. 43: 329-336. PMID 8288263 DOI: 10.1159/000154155 |
0.43 |
|
| 1993 |
Vieland VJ, Hodge SE, Lish JD, Adams P, Weissman MM. Segregation analysis of panic disorder Psychiatric Genetics. 3: 63-72. DOI: 10.1097/00041444-199322000-00001 |
0.373 |
|
| 1992 |
Vieland V, Greenberg DA, Hodge SE, Ott J. Linkage analysis of two-locus diseases under single-locus and two-locus analysis models. Cytogenetics and Cell Genetics. 59: 145-6. PMID 1737484 DOI: 10.1159/000133229 |
0.354 |
|
| 1992 |
Hodge SE, Mulvihill JJ. Do bilineal pedigrees represent a problem for linkage analysis? Basic principles and simulation results for single-gene diseases with no heterogeneity. Genetic Epidemiology. 9: 191-206. PMID 1521781 DOI: 10.1002/Gepi.1370090306 |
0.395 |
|
| 1990 |
Johnson WG, Hodge SE, Duvoisin R. Twin studies and the genetics of Parkinson's disease - a reappraisal Movement Disorders. 5: 187-194. PMID 2388635 DOI: 10.1002/Mds.870050302 |
0.347 |
|
| 1981 |
Haile RW, Iselius L, Hodge SE, Morton NE, Detels R. Segregation and linkage analysis of 40 multiplex multiple sclerosis families. Human Heredity. 31: 252-8. PMID 7287016 DOI: 10.1159/000153218 |
0.385 |
|
| 1980 |
Haile RW, Hodge SE, Visscher BR, Spence MA, Detels R, McAuliffe TL, Park MS, Dudley JP. Genetic susceptibility to multiple sclerosis: a linkage analysis with age-of-onset corrections. Clinical Genetics. 18: 160-7. PMID 7438496 DOI: 10.1111/J.1399-0004.1980.Tb00864.X |
0.395 |
|
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