| Year |
Citation |
Score |
| 2023 |
Vazzana KM, Musolf AM, Bailey-Wilson JE, Hiraki LT, Silverman ED, Scott C, Dalgard CL, Hasni S, Deng Z, Kaplan MJ, Lewandowski LB. Transmission disequilibrium analysis of whole genome data in childhood-onset systemic lupus erythematosus. Genes and Immunity. PMID 37488248 DOI: 10.1038/s41435-023-00214-x |
0.31 |
|
| 2022 |
Wijesiriwardhana P, Musolf AM, Bailey-Wilson JE, Wetthasinghe TK, Dissanayake VHW. Genome-wide linkage search for cancer susceptibility loci in a cohort of non BRCA1/2 families in Sri Lanka. Bmc Research Notes. 15: 190. PMID 35655316 DOI: 10.1186/s13104-022-06081-5 |
0.384 |
|
| 2021 |
Jiang Y, Chiu CY, Yan Q, Chen W, Gorin MB, Conley YP, Lakhal-Chaieb ML, Cook RJ, Amos CI, Wilson AF, Bailey-Wilson JE, McMahon FJ, Vazquez AI, Yuan A, Zhong X, et al. Gene-Based Association Testing of Dichotomous Traits With Generalized Functional Linear Mixed Models Using Extended Pedigrees: Applications to Age-Related Macular Degeneration. Journal of the American Statistical Association. 116: 531-545. PMID 34321704 DOI: 10.1080/01621459.2020.1799809 |
0.325 |
|
| 2021 |
Musolf AM, Simpson CL, Moiz BA, Pikielny CW, Middlebrooks CD, Mandal D, de Andrade M, Cole MD, Gaba C, Yang P, You M, Li Y, Kupert EY, Anderson MW, Schwartz AG, ... ... Bailey-Wilson JE, et al. Genetic variation and recurrent haplotypes on chromosome 6q23-25 risk locus in familial lung cancer. Cancer Research. PMID 33853833 DOI: 10.1158/0008-5472.CAN-20-3196 |
0.381 |
|
| 2020 |
Bailey-Wilson JE. A powerful new method for rare-variant analysis of quantitative traits in families. European Journal of Human Genetics : Ejhg. PMID 32958847 DOI: 10.1038/S41431-020-00731-7 |
0.375 |
|
| 2020 |
Delaney A, Burkholder AB, Lavender CA, Plummer L, Mericq V, Merino PM, Quinton R, Lewis KL, Meader BN, Albano A, Shaw ND, Welt CK, Martin KA, Seminara SB, Biesecker LG, ... Bailey-Wilson JE, et al. Increased Burden of Rare Sequence Variants in GnRH-Associated Genes in Women with Hypothalamic Amenorrhea. The Journal of Clinical Endocrinology and Metabolism. PMID 32870266 DOI: 10.1210/Clinem/Dgaa609 |
0.332 |
|
| 2020 |
Schaid DJ, McDonnell SK, FitzGerald LM, DeRycke L, Fogarty Z, Giles GG, MacInnis RJ, Southey MC, Nguyen-Dumont T, Cancel-Tassin G, Cussenot O, Whittemore AS, Sieh W, Ioannidis NM, Hsieh CL, ... ... Bailey-Wilson JE, et al. Two-stage Study of Familial Prostate Cancer by Whole-exome Sequencing and Custom Capture Identifies 10 Novel Genes Associated with the Risk of Prostate Cancer. European Urology. PMID 32800727 DOI: 10.1016/J.Eururo.2020.07.038 |
0.462 |
|
| 2020 |
Lewis DD, Wong S, Baker AS, Bailey-Wilson JE, Carpten JD, Cropp CD. Abstract C050: Deleterious coding variants in African American Hereditary Prostate Cancer Study (AAHPC) families Cancer Epidemiology, Biomarkers & Prevention. DOI: 10.1158/1538-7755.Disp18-C050 |
0.405 |
|
| 2020 |
Musolf AM, Simpson CL, Moiz BA, Andrade Md, Mandal D, Gaba C, Yang P, You M, Kupert EY, Anderson MW, Schwartz AG, Pinney SM, Amos CI, Bailey-Wilson JE. Abstract 37: Highly aggregated lung cancer families reveal a heterogeneous cause for a previous linkage signal on 6q Epidemiology. 80: 37-37. DOI: 10.1158/1538-7445.Am2020-37 |
0.493 |
|
| 2020 |
Middlebrooks C, Pantin K, Stacey M, Snyder C, Casey MJ, Shaw T, Bailey-Wilson JE, Lynch HT. Abstract 2300: Deleterious germline mutations in the BRCA1 gene are associated with increased risk for cancers of the female reproductive system other than breast and ovarian as well as other cancers Cancer Research. 80: 2300-2300. DOI: 10.1158/1538-7445.Am2020-2300 |
0.393 |
|
| 2020 |
Jiang Y, Chiu C, Yan Q, Chen W, Gorin MB, Conley YP, Lakhal-Chaieb ML, Cook RJ, Amos CI, Wilson AF, Bailey-Wilson JE, McMahon FJ, Vazquez AI, Yuan A, Zhong X, et al. Gene-Based Association Testing of Dichotomous Traits With Generalized Functional Linear Mixed Models Using Extended Pedigrees: Applications to Age-Related Macular Degeneration Journal of the American Statistical Association. 1-15. DOI: 10.1080/01621459.2020.1799809 |
0.332 |
|
| 2019 |
Musolf AM, Moiz BA, Sun H, Pikielny CW, Bossé Y, Mandal D, de Andrade M, Gaba C, Yang P, Li Y, You M, Govindan R, Wilson RK, Kupert EY, Anderson MW, ... ... Bailey-Wilson JE, et al. Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p and 4q. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 31826912 DOI: 10.1158/1055-9965.Epi-19-0887 |
0.443 |
|
| 2019 |
Chiu CY, Zhang B, Wang S, Shao J, Lakhal-Chaieb ML, Cook RJ, Wilson AF, Bailey-Wilson JE, Xiong M, Fan R. Gene-based association analysis of survival traits via functional regression-based mixed effect cox models for related samples. Genetic Epidemiology. PMID 31502722 DOI: 10.1002/Gepi.22254 |
0.327 |
|
| 2019 |
Musolf AM, Ho WSC, Long KA, Zhuang Z, Argersinger DP, Sun H, Moiz BA, Simpson CL, Mendelevich EG, Bogdanov EI, Bailey-Wilson JE, Heiss JD. Small posterior fossa in Chiari I malformation affected families is significantly linked to 1q43-44 and 12q23-24.11 using whole exome sequencing. European Journal of Human Genetics : Ejhg. PMID 31227808 DOI: 10.1038/S41431-019-0457-7 |
0.472 |
|
| 2019 |
Middlebrooks CD, Stacey ML, Li Q, Snyder C, Shaw TG, Richardson-Nelson T, Rendell M, Ferguson C, Silberstein P, Casey MJ, Bailey-Wilson JE, Lynch HT. Analysis of the CDKN2A gene in FAMMM Syndrome families reveals early age of onset for additional syndromic cancers. Cancer Research. PMID 30967399 DOI: 10.1158/0008-5472.Can-18-1580 |
0.422 |
|
| 2019 |
Musolf AM, Simpson CL, Alexander TA, Portas L, Murgia F, Ciner EB, Stambolian D, Bailey-Wilson JE. Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33. Human Genetics. PMID 30826882 DOI: 10.1007/S00439-019-01991-0 |
0.501 |
|
| 2019 |
Simpson CL, Musolf AM, Li Q, Portas L, Murgia F, Cordero RY, Cordero JB, Moiz BA, Holzinger ER, Middlebrooks CD, Lewis DD, Bailey-Wilson JE, Stambolian D. Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families. Bmc Medical Genetics. 20: 27. PMID 30704416 DOI: 10.1186/S12881-019-0752-8 |
0.456 |
|
| 2019 |
Delaney A, Plummer L, Burkholder A, Mericq M, Merino P, Quinton R, Lewis K, Meader B, Shaw N, Welt C, Martin K, Seminara S, Biesecker L, Bailey-Wilson J, Hall J. OR11-6 Rare Sequence Variants in GnRH-Associated Genes May Contribute to Variable Susceptibility to Environmental Stressors in Functional Hypothalamic Amenorrhea Journal of the Endocrine Society. 3. DOI: 10.1210/Js.2019-Or11-6 |
0.318 |
|
| 2019 |
Lewis DD, Wong S, Baker AS, Powell I, Carpten JD, Bailey-Wilson JE, Cropp C. Abstract 4240: Rare candidate variants shared among affected family members in the African American Hereditary Prostate Cancer Study families Cancer Research. DOI: 10.1158/1538-7445.Sabcs18-4240 |
0.448 |
|
| 2019 |
Musolf A, Sun H, Moiz BA, Pikielny CW, Andrade Md, Mandal D, Gaba C, Yang P, Li Y, You M, Wilson RK, Kupert EY, Anderson MW, Schwartz AG, Pinney SM, ... ... Bailey-Wilson JE, et al. Abstract 4176: Familial lung cancer exhibits multiple novel linked haplotypes within pedigrees Cancer Research. 79: 4176-4176. DOI: 10.1158/1538-7445.Sabcs18-4176 |
0.518 |
|
| 2019 |
Pikielny CW, Musolf AM, Andrade Md, Mandal D, Gaba C, Yang P, Li y, You M, Wilson R, Kupert EY, Anderson MW, Schwartz AG, Pinney SM, Granizo-Mackenzie AI, Liu Y, ... ... Bailey-Wilson JE, et al. Abstract LB-053: Familial studies identify variants in the E2A transcription factor as putative risk factors for lung cancer Cancer Research. 79. DOI: 10.1158/1538-7445.Am2019-Lb-053 |
0.473 |
|
| 2018 |
Chiu CY, Yuan F, Zhang BS, Yuan A, Li X, Fang HB, Lange K, Weeks DE, Wilson AF, Bailey-Wilson JE, Musolf AM, Stambolian D, Lakhal-Chaieb ML, Cook RJ, McMahon FJ, et al. Linear mixed models for association analysis of quantitative traits with next-generation sequencing data. Genetic Epidemiology. PMID 30537345 DOI: 10.1002/Gepi.22177 |
0.372 |
|
| 2018 |
Shane B, Pangilinan F, Mills JL, Fan R, Gong T, Cropp CD, Kim Y, Ueland PM, Bailey-Wilson JE, Wilson AF, Brody LC, Molloy AM. The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population. The American Journal of Clinical Nutrition. PMID 30339177 DOI: 10.1093/Ajcn/Nqy209 |
0.339 |
|
| 2018 |
Sabourin JA, Cropp CD, Sung H, Brody LC, Bailey-Wilson JE, Wilson AF. ComPaSS-GWAS: A method to reduce type I error in genome-wide association studies when replication data are not available. Genetic Epidemiology. PMID 30334581 DOI: 10.1002/Gepi.22168 |
0.358 |
|
| 2018 |
Bureau A, Begum F, Taub MA, Hetmanski JB, Parker MM, Albacha-Hejazi H, Scott AF, Murray JC, Marazita ML, Bailey-Wilson JE, Beaty TH, Ruczinski I. Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants. Genetic Epidemiology. PMID 30246882 DOI: 10.1002/Gepi.22155 |
0.446 |
|
| 2018 |
Chen Y, Gilbert MA, Grochowski CM, McEldrew D, Llewellyn J, Waisbourd-Zinman O, Hakonarson H, Bailey-Wilson JE, Russo P, Wells RG, Loomes KM, Spinner NB, Devoto M. A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1. Plos Genetics. 14: e1007532. PMID 30102696 DOI: 10.1371/Journal.Pgen.1007532 |
0.36 |
|
| 2018 |
Liu Y, Lusk CM, Cho MH, Silverman EK, Qiao D, Zhang R, Scheurer ME, Kheradmand F, Wheeler DA, Tsavachidis S, Armstrong G, Zhu D, Wistuba II, Chow CB, Behrens C, ... ... Bailey-Wilson J, et al. Rare Variants in Known Susceptibility Loci and Their Contribution to Risk of Lung Cancer. Journal of Thoracic Oncology : Official Publication of the International Association For the Study of Lung Cancer. PMID 29981437 DOI: 10.1016/J.Jtho.2018.06.016 |
0.413 |
|
| 2018 |
Byun J, Schwartz AG, Lusk C, Wenzlaff AS, de Andrade M, Mandal D, Gaba C, Yang P, You M, Kupert EY, Anderson MW, Han Y, Li Y, Qian D, Stilp A, ... ... Bailey-Wilson JE, et al. Genome-Wide Association Study of Familial Lung Cancer. Carcinogenesis. PMID 29924316 DOI: 10.1093/Carcin/Bgy080 |
0.44 |
|
| 2018 |
Shah RL, Li Q, Zhao W, Tedja MS, Tideman JWL, Khawaja AP, Fan Q, Yazar S, Williams KM, Verhoeven VJM, Xie J, Wang YX, Hess M, Nickels S, Lackner KJ, ... ... Bailey-Wilson JE, et al. A genome-wide association study of corneal astigmatism: The CREAM Consortium. Molecular Vision. 24: 127-142. PMID 29422769 DOI: 10.7892/Boris.114871 |
0.397 |
|
| 2018 |
Musolf AM, Simpson CL, Long KA, Moiz BA, Lewis DD, Middlebrooks CD, Portas L, Murgia F, Ciner EB, Bailey-Wilson JE, Stambolian D. Myopia in Chinese families shows linkage to 10q26.13. Molecular Vision. 24: 29-42. PMID 29383007 |
0.325 |
|
| 2018 |
Ngo B, Stacey M, Snyder C, Bailey-Wilson J, Rendell M, Lynch H. Concordant and discordant cancers in familial atypical multiple mole melanoma syndrome (FAMMM) with the CDKN2A mutation Journal of the American Academy of Dermatology. 79. DOI: 10.1016/J.Jaad.2018.05.373 |
0.377 |
|
| 2017 |
Lynch HT, Lanspa S, Shaw T, Casey MJ, Rendell M, Stacey M, Townley T, Snyder C, Hitchins M, Bailey-Wilson J. Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge. Familial Cancer. PMID 29071502 DOI: 10.1007/S10689-017-0053-3 |
0.395 |
|
| 2017 |
Holzinger ER, Li Q, Parker MM, Hetmanski JB, Marazita ML, Mangold E, Ludwig KU, Taub MA, Begum F, Murray JC, Albacha-Hejazi H, Alqosayer K, Al-Souki G, Albasha Hejazi A, Scott AF, ... ... Bailey-Wilson JE, et al. Analysis of sequence data to identify potential risk variants for oral clefts in multiplex families. Molecular Genetics & Genomic Medicine. 5: 570-579. PMID 28944239 DOI: 10.1002/Mgg3.320 |
0.404 |
|
| 2017 |
Musolf AM, Simpson CL, de Andrade M, Mandal D, Gaba C, Yang P, Li Y, You M, Kupert EY, Anderson MW, Schwartz AG, Pinney SM, Amos CI, Bailey-Wilson JE. Parametric Linkage Analysis Identifies Five Novel Genome-Wide Significant Loci for Familial Lung Cancer. Human Heredity. 82: 64-74. PMID 28817824 DOI: 10.1159/000479028 |
0.434 |
|
| 2017 |
Musolf AM, Simpson CL, Moiz BA, Long KA, Portas L, Murgia F, Ciner EB, Stambolian D, Bailey-Wilson JE. Caucasian Families Exhibit Significant Linkage of Myopia to Chromosome 11p. Investigative Ophthalmology & Visual Science. 58: 3547-3554. PMID 28715588 DOI: 10.1167/Iovs.16-21271 |
0.431 |
|
| 2017 |
Xie HM, Werner P, Stambolian D, Bailey-Wilson JE, Hakonarson H, White PS, Taylor DM, Goldmuntz E. Rare copy number variants in patients with congenital conotruncal heart defects. Birth Defects Research. 109: 271-295. PMID 28398664 DOI: 10.1002/Bdra.23609 |
0.311 |
|
| 2017 |
Afshari NA, Igo RP, Morris NJ, Stambolian D, Sharma S, Pulagam VL, Dunn S, Stamler JF, Truitt BJ, Rimmler J, Kuot A, Croasdale CR, Qin X, Burdon KP, Riazuddin SA, ... ... Bailey-Wilson JE, et al. Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy. Nature Communications. 8: 14898. PMID 28358029 DOI: 10.1038/Ncomms14898 |
0.381 |
|
| 2017 |
Larson NB, McDonnell S, Cannon Albright L, Teerlink C, Stanford J, Ostrander EA, Isaacs WB, Xu J, Cooney KA, Lange E, Schleutker J, Carpten JD, Powell I, Bailey-Wilson JE, Cussenot O, et al. gsSKAT: Rapid gene set analysis and multiple testing correction for rare-variant association studies using weighted linear kernels. Genetic Epidemiology. PMID 28211093 DOI: 10.1002/Gepi.22036 |
0.392 |
|
| 2017 |
Musolf AM, Simpson CL, de Andrade M, Mandal D, Gaba C, Yang P, Li Y, You M, Kupert EY, Anderson MW, Schwartz AG, Pinney SM, Amos CI, Bailey-Wilson JE. Familial Lung Cancer: A Brief History from the Earliest Work to the Most Recent Studies. Genes. 8. PMID 28106732 DOI: 10.3390/Genes8010036 |
0.468 |
|
| 2017 |
Ledet EM, Sartor O, Walter R, Bailey-Wilson J, Mandal D. Evidence of linkage in MSH6-associated region exclusive to high-risk African-American families with prostate cancer. Journal of Clinical Oncology. 35: 180-180. DOI: 10.1200/Jco.2017.35.6_Suppl.180 |
0.48 |
|
| 2017 |
Musolf AM, Simpson CL, Moiz BA, Middlebrooks C, Andrade Md, Mandal D, Gaba C, Yang P, Li Y, You M, Kupert EY, Anderson MW, Schwartz AG, Pinney SM, Amos CI, ... Bailey-Wilson JE, et al. Abstract 4290: A study in locus heterogeneity: Targeted sequencing analysis of 6q reveals multiple significant loci as the source of a previous linkage peak in familial lung cancer Epidemiology. 77: 4290-4290. DOI: 10.1158/1538-7445.Am2017-4290 |
0.442 |
|
| 2017 |
Bailey-Wilson JE, Musolf AM, Simpson CL, Andrade Md, Mandal D, Gaba CG, Yang P, You M, Kupert EY, Anderson MW, Schwartz AG, Pinney SM, Amos CI. Abstract 4268: Familial lung cancer is significantly linked to cancer-associated genes on five chromosomes Cancer Research. 77: 4268-4268. DOI: 10.1158/1538-7445.Am2017-4268 |
0.538 |
|
| 2016 |
Holzinger ER, Szymczak S, Malley J, Pugh EW, Ling H, Griffith S, Zhang P, Li Q, Cropp CD, Bailey-Wilson JE. Comparison of parametric and machine methods for variable selection in simulated Genetic Analysis Workshop 19 data. Bmc Proceedings. 10: 147-152. PMID 27980627 DOI: 10.1186/S12919-016-0021-1 |
0.351 |
|
| 2016 |
Chiu CY, Jung J, Wang Y, Weeks DE, Wilson AF, Bailey-Wilson JE, Amos CI, Mills JL, Boehnke M, Xiong M, Fan R. A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next-generation sequencing. Genetic Epidemiology. PMID 27917525 DOI: 10.1002/Gepi.22014 |
0.406 |
|
| 2016 |
Fan R, Chiu CY, Jung J, Weeks DE, Wilson AF, Bailey-Wilson JE, Amos CI, Chen Z, Mills JL, Xiong M. A Comparison Study of Fixed and Mixed Effect Models for Gene Level Association Studies of Complex Traits. Genetic Epidemiology. PMID 27374056 DOI: 10.1002/Gepi.21984 |
0.349 |
|
| 2016 |
Larson NB, McDonnell S, Albright LC, Teerlink C, Stanford J, Ostrander EA, Isaacs WB, Xu J, Cooney KA, Lange E, Schleutker J, Carpten JD, Powell I, Bailey-Wilson J, Cussenot O, et al. Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies. Genetic Epidemiology. PMID 27312771 DOI: 10.1002/Gepi.21983 |
0.384 |
|
| 2016 |
Fan Q, Guo X, Tideman JW, Williams KM, Yazar S, Hosseini SM, Howe LD, Pourcain BS, Evans DM, Timpson NJ, McMahon G, Hysi PG, Krapohl E, Wang YX, Jonas JB, ... ... Bailey-Wilson JE, et al. Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium. Scientific Reports. 6: 25853. PMID 27174397 DOI: 10.1038/Srep25853 |
0.375 |
|
| 2016 |
Molloy AM, Pangilinan F, Mills JL, Shane B, O'Neill MB, McGaughey DM, Velkova A, Abaan HO, Ueland PM, McNulty H, Ward M, Strain JJ, Cunningham C, Casey M, Cropp CD, ... ... Bailey-Wilson JE, et al. A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of Cobalamin. American Journal of Human Genetics. PMID 27132595 DOI: 10.1016/J.Ajhg.2016.03.005 |
0.325 |
|
| 2016 |
Szymczak S, Holzinger E, Dasgupta A, Malley JD, Molloy AM, Mills JL, Brody LC, Stambolian D, Bailey-Wilson JE. r2VIM: A new variable selection method for random forests in genome-wide association studies. Biodata Mining. 9: 7. PMID 26839594 DOI: 10.1186/S13040-016-0087-3 |
0.323 |
|
| 2016 |
Liu Y, Kheradmand F, Davis CF, Scheurer ME, Wheeler D, Tsavachidis S, Armstrong G, Simpson C, Mandal D, Kupert E, Anderson M, You M, Xiong D, Pikielny C, Schwartz AG, ... Bailey-Wilson J, et al. Focused Analysis of Exome Sequencing Data for Rare Germline Mutations in Familial and Sporadic Lung Cancer. Journal of Thoracic Oncology : Official Publication of the International Association For the Study of Lung Cancer. 11: 52-61. PMID 26762739 DOI: 10.1016/J.Jtho.2015.09.015 |
0.391 |
|
| 2016 |
Cropp CD, McDonnell SK, Middha S, DeRycke M, Karyadi DM, Schaid D, Thibodeau SN, Isaacs WB, Ostrander EA, Stanford J, Cooney KA, Bailey-Wilson JE, Carpten JD. Abstract B40: Rare variant discovery in known cancer genes from whole-exome sequencingof African American hereditary prostate cancer families Cancer Epidemiology, Biomarkers & Prevention. 25. DOI: 10.1158/1538-7755.Disp15-B40 |
0.496 |
|
| 2016 |
Musolf AM, Simpson CL, Andrade Md, Mandal D, Gaba C, Yang P, You M, Kupert EY, Anderson MW, Schwartz AG, Pinney SM, Amos CI, Bailey-Wilson JE. Abstract 2542: Chromatin remodeling gene ARID1B is linked to familial lung cancer Cancer Research. 76: 2542-2542. DOI: 10.1158/1538-7445.Am2016-2542 |
0.486 |
|
| 2015 |
Morrison MA, Magalhaes TR, Ramke J, Smith SE, Ennis S, Simpson CL, Portas L, Murgia F, Ahn J, Dardenne C, Mayne K, Robinson R, Morgan DJ, Brian G, Lee L, ... ... Bailey-Wilson JE, et al. Ancestry of the Timorese: age-related macular degeneration associated genotype and allele sharing among human populations from throughout the world. Frontiers in Genetics. 6: 238. PMID 26217379 DOI: 10.3389/Fgene.2015.00238 |
0.355 |
|
| 2015 |
Kember RL, Georgi B, Bailey-Wilson JE, Stambolian D, Paul SM, Bu?an M. Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder. Bmc Genetics. 16: 27. PMID 25887117 DOI: 10.1186/S12863-015-0184-1 |
0.387 |
|
| 2015 |
Sei Y, Zhao X, Forbes J, Szymczak S, Li Q, Trivedi A, Voellinger M, Joy G, Feng J, Whatley M, Jones MS, Harper UL, Marx SJ, Venkatesan AM, Chandrasekharappa SC, ... ... Bailey-Wilson JE, et al. A Hereditary Form of Small Intestinal Carcinoid Associated With a Germline Mutation in Inositol Polyphosphate Multikinase. Gastroenterology. 149: 67-78. PMID 25865046 DOI: 10.1053/J.Gastro.2015.04.008 |
0.403 |
|
| 2015 |
Wang Y, Liu A, Mills JL, Boehnke M, Wilson AF, Bailey-Wilson JE, Xiong M, Wu CO, Fan R. Pleiotropy analysis of quantitative traits at gene level by multivariate functional linear models. Genetic Epidemiology. 39: 259-75. PMID 25809955 DOI: 10.1002/Gepi.21895 |
0.344 |
|
| 2015 |
Li Q, Kim Y, Suktitipat B, Hetmanski JB, Marazita ML, Duggal P, Beaty TH, Bailey-Wilson JE. Gene-Gene Interaction Among WNT Genes for Oral Cleft in Trios. Genetic Epidemiology. 39: 385-94. PMID 25663376 DOI: 10.1002/Gepi.21888 |
0.347 |
|
| 2015 |
Xiong D, Wang Y, Kupert E, Simpson C, Pinney SM, Gaba CR, Mandal D, Schwartz AG, Yang P, de Andrade M, Pikielny C, Byun J, Li Y, Stambolian D, Spitz MR, ... ... Bailey-Wilson JE, et al. A recurrent mutation in PARK2 is associated with familial lung cancer. American Journal of Human Genetics. 96: 301-8. PMID 25640678 DOI: 10.1016/J.Ajhg.2014.12.016 |
0.403 |
|
| 2015 |
Li Q, Wojciechowski R, Simpson CL, Hysi PG, Verhoeven VJ, Ikram MK, Höhn R, Vitart V, Hewitt AW, Oexle K, Mäkelä KM, MacGregor S, Pirastu M, Fan Q, Cheng CY, ... ... Bailey-Wilson JE, et al. Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium. Human Genetics. 134: 131-46. PMID 25367360 DOI: 10.1007/S00439-014-1500-Y |
0.403 |
|
| 2015 |
Cross JL, Iben J, Simpson CL, Thurm A, Swedo S, Tierney E, Bailey-Wilson JE, Biesecker LG, Porter FD, Wassif CA. Determination of the allelic frequency in Smith-Lemli-Opitz syndrome by analysis of massively parallel sequencing data sets. Clinical Genetics. 87: 570-5. PMID 24813812 DOI: 10.1111/Cge.12425 |
0.368 |
|
| 2015 |
Ledet EM, Bailey-Wilson J, Sartor O, Li MM, Mandal D. Identification of susceptibility loci in hereditary prostate cancer families using copy number variation and linkage analysis. Journal of Clinical Oncology. 33: 232-232. DOI: 10.1200/Jco.2015.33.7_Suppl.232 |
0.481 |
|
| 2015 |
Toledo DM, Pinney SM, Mandal D, Andrade Md, Kupert E, Franks J, Gaba C, Simpson CL, You M, Anderson MW, Bailey-Wilson JE, Amos CI, Schwartz A. Abstract LB-189: Genetic Epidemiology of Lung Cancer Consortium: genome-wide association study of familial lung cancer cases: Epidemiology. 75. DOI: 10.1158/1538-7445.Am2015-Lb-189 |
0.401 |
|
| 2015 |
Liu Y, Kheradmand F, Scheurer M, Davis C, Wheeler D, Silverman E, Sanjay S, Tsavachidis S, Armstrong G, Kupert E, Anderson M, Li Y, Pikielny C, Bailey-Wilson JE, You M, et al. Abstract 4600: Target exome sequencing for disease-causing rare mutations in familial and sporadic lung cancer Cancer Research. 75: 4600-4600. DOI: 10.1158/1538-7445.Am2015-4600 |
0.454 |
|
| 2015 |
Stephens SH, Fleming PJ, Mitchell BD, Ambulos N, Bailey-Wilson JE, Chang C, Feliciano JL, Sausville EA, Edelman MJ. Abstract 4599: Somatic mutation profile differences of “driver” mutations in 26 oncogenic lung cancer genes between African American and European American non-small cell lung cancer patients Cancer Research. 75: 4599-4599. DOI: 10.1158/1538-7445.Am2015-4599 |
0.342 |
|
| 2015 |
Bailey-Wilson JE, Simpson CL, Pinney SM, Andrade Md, Gaba C, Yang P, You M, Kupert EY, Schwartz AG, Mandal D, Amos CI, Anderson MW. Abstract 2757: Evaluation ofEYA4as a candidate risk locus in familial lung cancer families linked to 6q Cancer Research. 75: 2757-2757. DOI: 10.1158/1538-7445.Am2015-2757 |
0.479 |
|
| 2015 |
Ledet E, Wood K, Bailey-Wilson J, Sartor O, Li M, Mandal D. Mp66-10 Characterization Of Susceptibility Loci In Hereditary Prostate Cancer Families Using Copy Number Variation And Linkage Analysis The Journal of Urology. 193. DOI: 10.1016/J.Juro.2015.02.2363 |
0.33 |
|
| 2014 |
Szymczak S, Simpson CL, Cropp CD, Bailey-Wilson JE. False-positive rates in two-point parametric linkage analysis. Bmc Proceedings. 8: S110. PMID 25519363 DOI: 10.1186/1753-6561-8-S1-S110 |
0.394 |
|
| 2014 |
Cropp CD, Robbins CM, Sheng X, Hennis AJ, Carpten JD, Waterman L, Worrell R, Schwantes-An TH, Trent JM, Haiman CA, Leske MC, Wu SY, Bailey-Wilson JE, Nemesure B. 8q24 risk alleles and prostate cancer in African-Barbadian men. The Prostate. 74: 1579-88. PMID 25252079 DOI: 10.1002/Pros.22871 |
0.433 |
|
| 2014 |
Simpson CL, Wojciechowski R, Oexle K, Murgia F, Portas L, Li X, Verhoeven VJ, Vitart V, Schache M, Hosseini SM, Hysi PG, Raffel LJ, Cotch MF, Chew E, Klein BE, ... ... Bailey-Wilson JE, et al. Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. Plos One. 9: e107110. PMID 25233373 DOI: 10.1371/Journal.Pone.0107110 |
0.377 |
|
| 2014 |
Fan R, Wang Y, Mills JL, Carter TC, Lobach I, Wilson AF, Bailey-Wilson JE, Weeks DE, Xiong M. Generalized functional linear models for gene-based case-control association studies. Genetic Epidemiology. 38: 622-37. PMID 25203683 DOI: 10.1002/Gepi.21840 |
0.37 |
|
| 2014 |
Hysi PG, Cheng CY, Springelkamp H, Macgregor S, Bailey JN, Wojciechowski R, Vitart V, Nag A, Hewitt AW, Höhn R, Venturini C, Mirshahi A, Ramdas WD, Thorleifsson G, Vithana E, ... ... Bailey-Wilson JE, et al. Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma. Nature Genetics. 46: 1126-30. PMID 25173106 DOI: 10.1038/Ng.3087 |
0.402 |
|
| 2014 |
Bureau A, Parker MM, Ruczinski I, Taub MA, Marazita ML, Murray JC, Mangold E, Noethen MM, Ludwig KU, Hetmanski JB, Bailey-Wilson JE, Cropp CD, Li Q, Szymczak S, Albacha-Hejazi H, et al. Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts. Genetics. 197: 1039-44. PMID 24793288 DOI: 10.1534/Genetics.114.165225 |
0.447 |
|
| 2014 |
Bureau A, Younkin SG, Parker MM, Bailey-Wilson JE, Marazita ML, Murray JC, Mangold E, Albacha-Hejazi H, Beaty TH, Ruczinski I. Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. Bioinformatics (Oxford, England). 30: 2189-96. PMID 24740360 DOI: 10.1093/Bioinformatics/Btu198 |
0.433 |
|
| 2014 |
Teerlink CC, Thibodeau SN, McDonnell SK, Schaid DJ, Rinckleb A, Maier C, Vogel W, Cancel-Tassin G, Egrot C, Cussenot O, Foulkes WD, Giles GG, Hopper JL, Severi G, Eeles R, ... ... Bailey-Wilson J, et al. Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease. Human Genetics. 133: 347-56. PMID 24162621 DOI: 10.1007/S00439-013-1384-2 |
0.483 |
|
| 2013 |
Simpson CL, Wojciechowski R, Yee SS, Soni P, Bailey-Wilson JE, Stambolian D. Regional replication of association with refractive error on 15q14 and 15q25 in the Age-Related Eye Disease Study cohort. Molecular Vision. 19: 2173-86. PMID 24227913 |
0.336 |
|
| 2013 |
Cheng CY, Schache M, Ikram MK, Young TL, Guggenheim JA, Vitart V, MacGregor S, Verhoeven VJ, Barathi VA, Liao J, Hysi PG, Bailey-Wilson JE, St Pourcain B, Kemp JP, McMahon G, et al. Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. American Journal of Human Genetics. 93: 264-77. PMID 24144296 DOI: 10.1016/J.Ajhg.2013.06.016 |
0.337 |
|
| 2013 |
Fan R, Wang Y, Mills JL, Wilson AF, Bailey-Wilson JE, Xiong M. Functional linear models for association analysis of quantitative traits. Genetic Epidemiology. 37: 726-42. PMID 24130119 DOI: 10.1002/Gepi.21757 |
0.407 |
|
| 2013 |
Stambolian D, Wojciechowski R, Oexle K, Pirastu M, Li X, Raffel LJ, Cotch MF, Chew EY, Klein B, Klein R, Wong TY, Simpson CL, Klaver CC, van Duijn CM, Verhoeven VJ, ... ... Bailey-Wilson JE, et al. Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error. Human Molecular Genetics. 22: 2754-64. PMID 23474815 DOI: 10.1093/Hmg/Ddt116 |
0.42 |
|
| 2013 |
Verhoeven VJ, Hysi PG, Wojciechowski R, Fan Q, Guggenheim JA, Höhn R, MacGregor S, Hewitt AW, Nag A, Cheng CY, Yonova-Doing E, Zhou X, Ikram MK, Buitendijk GH, McMahon G, ... ... Bailey-Wilson JE, et al. Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nature Genetics. 45: 314-8. PMID 23396134 DOI: 10.1038/Ng.2554 |
0.388 |
|
| 2013 |
Desch KC, Ozel AB, Siemieniak D, Kalish Y, Shavit JA, Thornburg CD, Sharathkumar AA, McHugh CP, Laurie CC, Crenshaw A, Mirel DB, Kim Y, Cropp CD, Molloy AM, Kirke PN, ... Bailey-Wilson JE, et al. Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association. Proceedings of the National Academy of Sciences of the United States of America. 110: 588-93. PMID 23267103 DOI: 10.1073/Pnas.1219885110 |
0.433 |
|
| 2013 |
Wojciechowski R, Yee SS, Simpson CL, Bailey-Wilson JE, Stambolian D. Matrix metalloproteinases and educational attainment in refractive error: evidence of gene-environment interactions in the Age-Related Eye Disease Study. Ophthalmology. 120: 298-305. PMID 23098370 DOI: 10.1016/J.Ophtha.2012.07.078 |
0.303 |
|
| 2013 |
Xu J, Lange EM, Lu L, Zheng SL, Wang Z, Thibodeau SN, Cannon-Albright LA, Teerlink CC, Camp NJ, Johnson AM, Zuhlke KA, Stanford JL, Ostrander EA, Wiley KE, Isaacs SD, ... ... Bailey-Wilson JE, et al. HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG). Human Genetics. 132: 5-14. PMID 23064873 DOI: 10.1007/S00439-012-1229-4 |
0.464 |
|
| 2013 |
Simpson CL, Cropp CD, Wahlfors T, George A, Jones MS, Harper U, Ponciano-Jackson D, Tammela T, Schleutker J, Bailey-Wilson JE. Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysis. European Journal of Human Genetics : Ejhg. 21: 437-43. PMID 22948022 DOI: 10.1038/Ejhg.2012.185 |
0.512 |
|
| 2013 |
Cropp CD, Simpson CL, Wahlfors T, George A, Jones MS, Harper U, Ponciano-Jackson D, Tammela T, Schleutker J, Bailey-Wilson JE. Abstract 3648: Unraveling phenotype heterogeneity in prostate cancer susceptibility in Finland utilizing covariate-based analysis. Cancer Research. 73: 3648-3648. DOI: 10.1158/1538-7445.Am2013-3648 |
0.513 |
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| 2013 |
Verhoeven VJM, Hysi PG, Wojciechowski R, Fan Q, Guggenheim JA, Höhn R, MacGregor S, Hewitt AW, Nag A, Cheng CY, Yonova-Doing E, Zhou X, Ikram MK, Buitendijk GHS, McMahon G, ... ... Bailey-Wilson JE, et al. Erratum: Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (Nature Genetics (2013) 45 (314-318)) Nature Genetics. 45: 712-712. DOI: 10.1038/Ng0613-712B |
0.382 |
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| 2012 |
Bailey-Wilson JE, Childs EJ, Cropp CD, Schaid DJ, Xu J, Camp NJ, Cannon-Albright LA, Farnham JM, George A, Powell I, Carpten JD, Giles GG, Hopper JL, Severi G, English DR, et al. Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families. Bmc Medical Genetics. 13: 46. PMID 22712434 DOI: 10.1186/1471-2350-13-46 |
0.527 |
|
| 2012 |
Verhoeven VJ, Hysi PG, Saw SM, Vitart V, Mirshahi A, Guggenheim JA, Cotch MF, Yamashiro K, Baird PN, Mackey DA, Wojciechowski R, Ikram MK, Hewitt AW, Duggal P, Janmahasatian S, ... ... Bailey-Wilson JE, et al. Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium. Human Genetics. 131: 1467-80. PMID 22665138 DOI: 10.1007/S00439-012-1176-0 |
0.39 |
|
| 2012 |
Ledet EM, Sartor O, Rayford W, Bailey-Wilson JE, Mandal DM. Suggestive evidence of linkage identified at chromosomes 12q24 and 2p16 in African American prostate cancer families from Louisiana. The Prostate. 72: 938-47. PMID 22615067 DOI: 10.1002/Pros.21496 |
0.452 |
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| 2012 |
Cabral WA, Barnes AM, Adeyemo A, Cushing K, Chitayat D, Porter FD, Panny SR, Gulamali-Majid F, Tishkoff SA, Rebbeck TR, Gueye SM, Bailey-Wilson JE, Brody LC, Rotimi CN, Marini JC. A founder mutation in LEPRE1 carried by 1.5% of West Africans and 0.4% of African Americans causes lethal recessive osteogenesis imperfecta. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 14: 543-51. PMID 22281939 DOI: 10.1038/Gim.2011.44 |
0.321 |
|
| 2012 |
Lu L, Cancel-Tassin G, Valeri A, Cussenot O, Lange EM, Cooney KA, Farnham JM, Camp NJ, Cannon-Albright LA, Tammela TL, Schleutker J, Hoegel J, Herkommer K, Maier C, Vogel W, ... ... Bailey-Wilson JE, et al. Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG. The Prostate. 72: 410-26. PMID 21748754 DOI: 10.1002/Pros.21443 |
0.533 |
|
| 2012 |
Jain M, Vélez JI, Acosta MT, Palacio LG, Balog J, Roessler E, Pineda D, Londoño AC, Palacio JD, Arbelaez A, Lopera F, Elia J, Hakonarson H, Seitz C, Freitag CM, ... ... Bailey-Wilson JE, et al. A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD. Molecular Psychiatry. 17: 741-7. PMID 21606926 DOI: 10.1038/Mp.2011.59 |
0.393 |
|
| 2012 |
Amos C, Bailey-Wilson J, Pinney S, Andrada Md, Gaba C, Mandal D, You M, Spitz M, Anderson M. Abstract A106: Optimal strategies for selecting samples for sequencing families with a common cancer: The Genetic Epidemiology of Lung Cancer Consortium. Cancer Prevention Research. 5. DOI: 10.1158/1940-6207.Prev-12-A106 |
0.429 |
|
| 2011 |
Sung H, Kim Y, Cai J, Cropp CD, Simpson CL, Li Q, Perry BC, Sorant AJ, Bailey-Wilson JE, Wilson AF. Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression. Bmc Proceedings. 5: S15. PMID 22373501 DOI: 10.1186/1753-6561-5-S9-S15 |
0.409 |
|
| 2011 |
Kim Y, Li Q, Cropp CD, Sung H, Cai J, Simpson CL, Perry B, Dasgupta A, Malley JD, Wilson AF, Bailey-Wilson JE. Performance of random forests and logic regression methods using mini-exome sequence data. Bmc Proceedings. 5: S104. PMID 22373484 DOI: 10.1186/1753-6561-5-S9-S104 |
0.35 |
|
| 2011 |
Simpson CL, Justice CM, Krishnan M, Wojciechowski R, Sung H, Cai J, Green T, Lewis D, Behneman D, Wilson AF, Bailey-Wilson JE. Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data. Bmc Proceedings. 5: S83. PMID 22373393 DOI: 10.1186/1753-6561-5-S9-S83 |
0.475 |
|
| 2011 |
Ghosh S, Bickeböller H, Bailey J, Bailey-Wilson JE, Cantor R, Culverhouse R, Daw W, Destefano AL, Engelman CD, Hinrichs A, Houwing-Duistermaat J, König IR, Kent J, Laird N, Pankratz N, et al. Identifying rare variants from exome scans: the GAW17 experience. Bmc Proceedings. 5: S1. PMID 22373325 DOI: 10.1186/1753-6561-5-S9-S1 |
0.367 |
|
| 2011 |
Bailey-Wilson JE, Wilson AF. Linkage analysis in the next-generation sequencing era. Human Heredity. 72: 228-36. PMID 22189465 DOI: 10.1159/000334381 |
0.419 |
|
| 2011 |
Bailey-Wilson JE, Brennan JS, Bull SB, Culverhouse R, Kim Y, Jiang Y, Jung J, Li Q, Lamina C, Liu Y, Mägi R, Niu YS, Simpson CL, Wang L, Yilmaz YE, et al. Regression and data mining methods for analyses of multiple rare variants in the Genetic Analysis Workshop 17 mini-exome data. Genetic Epidemiology. 35: S92-100. PMID 22128066 DOI: 10.1002/Gepi.20657 |
0.396 |
|
| 2011 |
Dasgupta A, Sun YV, König IR, Bailey-Wilson JE, Malley JD. Brief review of regression-based and machine learning methods in genetic epidemiology: the Genetic Analysis Workshop 17 experience. Genetic Epidemiology. 35: S5-11. PMID 22128059 DOI: 10.1002/Gepi.20642 |
0.333 |
|
| 2011 |
Klein AP, Duggal P, Lee KE, Cheng CY, Klein R, Bailey-Wilson JE, Klein BE. Linkage analysis of quantitative refraction and refractive errors in the Beaver Dam Eye Study. Investigative Ophthalmology & Visual Science. 52: 5220-5. PMID 21571680 DOI: 10.1167/Iovs.10-7096 |
0.383 |
|
| 2011 |
Catalona WJ, Bailey-Wilson JE, Camp NJ, Chanock SJ, Cooney KA, Easton DF, Eeles RA, FitzGerald LM, Freedman ML, Gudmundsson J, Kittles RA, Margulies EH, McGuire BB, Ostrander EA, Rebbeck TR, et al. National Cancer Institute Prostate Cancer Genetics Workshop. Cancer Research. 71: 3442-6. PMID 21558387 DOI: 10.1158/0008-5472.Can-11-0314 |
0.437 |
|
| 2011 |
Cropp CD, Simpson CL, Wahlfors T, Ha N, George A, Jones MS, Harper U, Ponciano-Jackson D, Green TA, Tammela TL, Bailey-Wilson J, Schleutker J. Genome-wide linkage scan for prostate cancer susceptibility in Finland: evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21-q22. International Journal of Cancer. Journal International Du Cancer. 129: 2400-7. PMID 21207418 DOI: 10.1002/Ijc.25906 |
0.521 |
|
| 2011 |
Ricks-Santi LJ, Mason T, Abbas M, Dunston GM, Kolluri S, Gold B, Im K, Lautenberger J, Dean M, Bailey-Wilson J, Carpten J, Ahaghotu C. Abstract A69: Identification of prostate cancer genes in the African American Hereditary Prostate Cancer (AAHPC) study Cancer Epidemiology, Biomarkers & Prevention. 20. DOI: 10.1158/1055-9965.Disp-11-A69 |
0.505 |
|
| 2010 |
Fang S, Pinney SM, Bailey-Wilson JE, de Andrade MA, Li Y, Kupert E, You M, Schwartz AG, Yang P, Anderson MW, Amos CI. Ordered subset analysis identifies loci influencing lung cancer risk on chromosomes 6q and 12q. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 19: 3157-66. PMID 21030603 DOI: 10.1158/1055-9965.Epi-10-0792 |
0.494 |
|
| 2010 |
Agalliu I, Leanza SM, Smith L, Trent JM, Carpten JD, Bailey-Wilson JE, Burk RD. Contribution of HPC1 (RNASEL) and HPCX variants to prostate cancer in a founder population. The Prostate. 70: 1716-27. PMID 20564318 DOI: 10.1002/Pros.21207 |
0.424 |
|
| 2010 |
Wojciechowski R, Bailey-Wilson JE, Stambolian D. Association of matrix metalloproteinase gene polymorphisms with refractive error in Amish and Ashkenazi families. Investigative Ophthalmology & Visual Science. 51: 4989-95. PMID 20484597 DOI: 10.1167/Iovs.10-5474 |
0.332 |
|
| 2010 |
Liu P, Yang P, Wu X, Vikis HG, Lu Y, Wang Y, Schwartz AG, Pinney SM, de Andrade M, Gazdar A, Gaba C, Mandal D, Lee J, Kupert E, Seminara D, ... ... Bailey-Wilson JE, et al. A second genetic variant on chromosome 15q24-25.1 associates with lung cancer. Cancer Research. 70: 3128-35. PMID 20395203 DOI: 10.1158/0008-5472.Can-09-3583 |
0.401 |
|
| 2010 |
Christensen GB, Baffoe-Bonnie AB, George A, Powell I, Bailey-Wilson JE, Carpten JD, Giles GG, Hopper JL, Severi G, English DR, Foulkes WD, Maehle L, Moller P, Eeles R, Easton D, et al. Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for Prostate Cancer Genetics using novel sumLINK and sumLOD analyses. The Prostate. 70: 735-44. PMID 20333727 DOI: 10.1002/Pros.21106 |
0.502 |
|
| 2010 |
Amos CI, Pinney SM, Li Y, Kupert E, Lee J, de Andrade MA, Yang P, Schwartz AG, Fain PR, Gazdar A, Minna J, Wiest JS, Zeng D, Rothschild H, Mandal D, ... ... Bailey-Wilson JE, et al. A susceptibility locus on chromosome 6q greatly increases lung cancer risk among light and never smokers. Cancer Research. 70: 2359-67. PMID 20215501 DOI: 10.1158/0008-5472.Can-09-3096 |
0.354 |
|
| 2010 |
Deka R, Koller DL, Lai D, Indugula SR, Sun G, Woo D, Sauerbeck L, Moomaw CJ, Hornung R, Connolly ES, Anderson C, Rouleau G, Meissner I, Bailey-Wilson JE, Huston J, et al. The relationship between smoking and replicated sequence variants on chromosomes 8 and 9 with familial intracranial aneurysm. Stroke; a Journal of Cerebral Circulation. 41: 1132-7. PMID 20190001 DOI: 10.1161/Strokeaha.109.574640 |
0.337 |
|
| 2010 |
Liu P, Vikis HG, Lu Y, Wang Y, Schwartz AG, Pinney SM, Yang P, de Andrade M, Gazdar A, Gaba C, Mandal D, Lee J, Kupert E, Seminara D, Minna J, ... Bailey-Wilson JE, et al. Cumulative effect of multiple loci on genetic susceptibility to familial lung cancer. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 19: 517-24. PMID 20142248 DOI: 10.1158/1055-9965.Epi-09-0791 |
0.466 |
|
| 2010 |
Cheng CY, Reich D, Coresh J, Boerwinkle E, Patterson N, Li M, North KE, Tandon A, Bailey-Wilson JE, Wilson JG, Kao WH. Admixture mapping of obesity-related traits in African Americans: the Atherosclerosis Risk in Communities (ARIC) Study. Obesity (Silver Spring, Md.). 18: 563-72. PMID 19696751 DOI: 10.1038/Oby.2009.282 |
0.329 |
|
| 2010 |
Cheng CY, Lee KE, Duggal P, Moore EL, Wilson AF, Klein R, Bailey-Wilson JE, Klein BE. Genome-wide linkage analysis of multiple metabolic factors: evidence of genetic heterogeneity. Obesity (Silver Spring, Md.). 18: 146-52. PMID 19444228 DOI: 10.1038/Oby.2009.142 |
0.402 |
|
| 2009 |
Wallis D, Arcos-Burgos M, Jain M, Castellanos FX, Palacio JD, Pineda D, Lopera F, Stanescu H, Pineda D, Berg K, Palacio LG, Bailey-Wilson JE, Muenke M. Polymorphisms in the neural nicotinic acetylcholine receptor α4 subunit (CHRNA4) are associated with ADHD in a genetic isolate. Attention Deficit and Hyperactivity Disorders. 1: 19-24. PMID 21432576 DOI: 10.1007/S12402-009-0003-5 |
0.335 |
|
| 2009 |
Kim Y, Wojciechowski R, Sung H, Mathias RA, Wang L, Klein AP, Lenroot RK, Malley J, Bailey-Wilson JE. Evaluation of random forests performance for genome-wide association studies in the presence of interaction effects. Bmc Proceedings. 3: S64. PMID 20018058 DOI: 10.1186/1753-6561-3-S7-S64 |
0.337 |
|
| 2009 |
Liu Y, Liu P, Wen W, James MA, Wang Y, Bailey-Wilson JE, Amos CI, Pinney SM, Yang P, de Andrade M, Petersen GM, Wiest JS, Fain PR, Schwartz AG, Gazdar A, et al. Haplotype and cell proliferation analyses of candidate lung cancer susceptibility genes on chromosome 15q24-25.1. Cancer Research. 69: 7844-50. PMID 19789337 DOI: 10.1158/0008-5472.Can-09-1833 |
0.399 |
|
| 2009 |
Jun G, Guo H, Klein BE, Klein R, Wang JJ, Mitchell P, Miao H, Lee KE, Joshi T, Buck M, Chugha P, Bardenstein D, Klein AP, Bailey-Wilson JE, Gong X, et al. EPHA2 is associated with age-related cortical cataract in mice and humans. Plos Genetics. 5: e1000584. PMID 19649315 DOI: 10.1371/Journal.Pgen.1000584 |
0.321 |
|
| 2009 |
Wojciechowski R, Bailey-Wilson JE, Stambolian D. Fine-mapping of candidate region in Amish and Ashkenazi families confirms linkage of refractive error to a QTL on 1p34-p36. Molecular Vision. 15: 1398-406. PMID 19626131 |
0.308 |
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| 2009 |
Klein AP, Suktitipat B, Duggal P, Lee KE, Klein R, Bailey-Wilson JE, Klein BE. Heritability analysis of spherical equivalent, axial length, corneal curvature, and anterior chamber depth in the Beaver Dam Eye Study. Archives of Ophthalmology (Chicago, Ill. : 1960). 127: 649-55. PMID 19433716 DOI: 10.1001/Archophthalmol.2009.61 |
0.358 |
|
| 2009 |
You M, Wang D, Liu P, Vikis H, James M, Lu Y, Wang Y, Wang M, Chen Q, Jia D, Liu Y, Wen W, Yang P, Sun Z, Pinney SM, ... ... Bailey-Wilson JE, et al. Fine mapping of chromosome 6q23-25 region in familial lung cancer families reveals RGS17 as a likely candidate gene. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 15: 2666-74. PMID 19351763 DOI: 10.1158/1078-0432.Ccr-08-2335 |
0.477 |
|
| 2009 |
Wojciechowski R, Stambolian D, Ciner E, Ibay G, Holmes TN, Bailey-Wilson JE. Genomewide linkage scans for ocular refraction and meta-analysis of four populations in the Myopia Family Study. Investigative Ophthalmology & Visual Science. 50: 2024-32. PMID 19151385 DOI: 10.1167/Iovs.08-2848 |
0.441 |
|
| 2009 |
Foroud T, Sauerbeck L, Brown R, Anderson C, Woo D, Kleindorfer D, Flaherty ML, Deka R, Hornung R, Meissner I, Bailey-Wilson JE, Langefeld C, Rouleau G, Connolly ES, Lai D, et al. Genome screen in familial intracranial aneurysm. Bmc Medical Genetics. 10: 3. PMID 19144135 DOI: 10.1186/1471-2350-10-3 |
0.34 |
|
| 2009 |
Ciner E, Ibay G, Wojciechowski R, Dana D, Holmes TN, Bailey-Wilson JE, Stambolian D. Genome-wide scan of African-American and white families for linkage to myopia. American Journal of Ophthalmology. 147: 512-517.e2. PMID 19026404 DOI: 10.1016/J.Ajo.2008.09.004 |
0.388 |
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| 2009 |
Weyandt J, Snyder C, Lynch H, Gillanders E, Holmes T, Bailey-Wilson J, Ellsworth R. Identification of BRCA1 and BRCA2 genetic modifiers. Cancer Research. 69: 1040. DOI: 10.1158/0008-5472.Sabcs-1040 |
0.69 |
|
| 2008 |
Duggal P, Gillanders EM, Holmes TN, Bailey-Wilson JE. Establishing an adjusted p-value threshold to control the family-wide type 1 error in genome wide association studies. Bmc Genomics. 9: 516. PMID 18976480 DOI: 10.1186/1471-2164-9-516 |
0.666 |
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| 2008 |
Liu P, Vikis HG, Wang D, Lu Y, Wang Y, Schwartz AG, Pinney SM, Yang P, de Andrade M, Petersen GM, Wiest JS, Fain PR, Gazdar A, Gaba C, Rothschild H, ... ... Bailey-Wilson JE, et al. Familial aggregation of common sequence variants on 15q24-25.1 in lung cancer. Journal of the National Cancer Institute. 100: 1326-30. PMID 18780872 DOI: 10.1093/Jnci/Djn268 |
0.435 |
|
| 2008 |
Siltanen S, Syrjäkoski K, Fagerholm R, Ikonen T, Lipman P, Mallott J, Holli K, Tammela TL, Järvinen HJ, Mecklin JP, Aittomäki K, Blomqvist C, Bailey-Wilson JE, Nevanlinna H, Aaltonen LA, et al. ARLTS1 germline variants and the risk for breast, prostate, and colorectal cancer. European Journal of Human Genetics : Ejhg. 16: 983-91. PMID 18337727 DOI: 10.1038/Ejhg.2008.43 |
0.461 |
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| 2008 |
Foroud T, Sauerbeck L, Brown R, Anderson C, Woo D, Kleindorfer D, Flaherty ML, Deka R, Hornung R, Meissner I, Bailey-Wilson JE, Rouleau G, Connolly ES, Lai D, Koller DL, et al. Genome screen to detect linkage to intracranial aneurysm susceptibility genes: the Familial Intracranial Aneurysm (FIA) study. Stroke; a Journal of Cerebral Circulation. 39: 1434-40. PMID 18323491 DOI: 10.1161/Strokeaha.107.502930 |
0.382 |
|
| 2008 |
Ciner E, Wojciechowski R, Ibay G, Bailey-Wilson JE, Stambolian D. Genomewide scan of ocular refraction in African-American families shows significant linkage to chromosome 7p15. Genetic Epidemiology. 32: 454-63. PMID 18293391 DOI: 10.1002/Gepi.20318 |
0.491 |
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| 2008 |
Mandal DM, Sartor O, Halton SL, Mercante DE, Bailey-Wilson JE, Rayford W. Recruitment strategies and comparison of prostate cancer-specific clinical data on African-American and Caucasian males with and without family history Prostate Cancer and Prostatic Diseases. 11: 274-279. PMID 18268528 DOI: 10.1038/Pcan.2008.5 |
0.437 |
|
| 2008 |
Kim Y, Duggal P, Gillanders EM, Kim H, Bailey-Wilson JE. Examining the effect of linkage disequilibrium between markers on the Type I error rate and power of nonparametric multipoint linkage analysis of two-generation and multigenerational pedigrees in the presence of missing genotype data. Genetic Epidemiology. 32: 41-51. PMID 17685456 DOI: 10.1002/Gepi.20260 |
0.634 |
|
| 2007 |
Kim Y, Doan BQ, Duggal P, Bailey-Wilson JE. Normalization of microarray expression data using within-pedigree pool and its effect on linkage analysis. Bmc Proceedings. 1: S152. PMID 18466497 DOI: 10.1186/1753-6561-1-S1-S152 |
0.416 |
|
| 2007 |
Camp NJ, Cannon-Albright LA, Farnham JM, Baffoe-Bonnie AB, George A, Powell I, Bailey-Wilson JE, Carpten JD, Giles GG, Hopper JL, Severi G, English DR, Foulkes WD, Maehle L, Moller P, et al. Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics. Human Molecular Genetics. 16: 1271-8. PMID 17478474 DOI: 10.1093/Hmg/Ddm075 |
0.482 |
|
| 2007 |
Klein AP, Duggal P, Lee KE, Klein R, Bailey-Wilson JE, Klein BE. Confirmation of linkage to ocular refraction on chromosome 22q and identification of a novel linkage region on 1q. Archives of Ophthalmology (Chicago, Ill. : 1960). 125: 80-5. PMID 17210856 DOI: 10.1001/Archopht.125.1.80 |
0.405 |
|
| 2007 |
Duggal P, Klein AP, Lee KE, Klein R, Klein BE, Bailey-Wilson JE. Identification of novel genetic loci for intraocular pressure: a genomewide scan of the Beaver Dam Eye Study. Archives of Ophthalmology (Chicago, Ill. : 1960). 125: 74-9. PMID 17210855 DOI: 10.1001/Archopht.125.1.74 |
0.376 |
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| 2007 |
Wang M, Vikis HG, Wang Y, Jia D, Wang D, Bierut LJ, Bailey-Wilson JE, Amos CI, Pinney SM, Petersen GM, de Andrade M, Yang P, Wiest JS, Fain PR, Schwartz AG, et al. Identification of a novel tumor suppressor gene p34 on human chromosome 6q25.1. Cancer Research. 67: 93-9. PMID 17210687 DOI: 10.1158/0008-5472.Can-06-2723 |
0.434 |
|
| 2007 |
Pakkanen S, Baffoe-Bonnie AB, Matikainen MP, Koivisto PA, Tammela TL, Deshmukh S, Ou L, Bailey-Wilson JE, Schleutker J. Segregation analysis of 1,546 prostate cancer families in Finland shows recessive inheritance. Human Genetics. 121: 257-67. PMID 17203302 DOI: 10.1007/S00439-006-0310-2 |
0.479 |
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| 2007 |
Seppälä EH, Autio V, Duggal P, Ikonen T, Stenman UH, Auvinen A, Bailey-Wilson JE, Tammela TL, Schleutker J. KLF6 IVS1 -27G>A variant and the risk of prostate cancer in Finland. European Urology. 52: 1076-81. PMID 17125911 DOI: 10.1016/J.Eururo.2006.11.019 |
0.379 |
|
| 2007 |
Baffoe-Bonnie AB, Kittles RA, Gillanders E, Ou L, George A, Robbins C, Ahaghotu C, Bennett J, Boykin W, Hoke G, Mason T, Pettaway C, Vijayakumar S, Weinrich S, Jones MP, ... ... Bailey-Wilson JE, et al. Genome-wide linkage of 77 families from the African American Hereditary Prostate Cancer study (AAHPC). The Prostate. 67: 22-31. PMID 17031815 DOI: 10.1002/Pros.20456 |
0.711 |
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| 2006 |
Stambolian D, Ibay G, Reider L, Dana D, Moy C, Schlifka M, Holmes TN, Ciner E, Bailey-Wilson JE. Genome-wide scan of additional Jewish families confirms linkage of a myopia susceptibility locus to chromosome 22q12. Molecular Vision. 12: 1499-505. PMID 17167407 |
0.313 |
|
| 2006 |
Marroni F, Pichler I, De Grandi A, Beu Volpato C, Vogl FD, Pinggera GK, Bailey-wilson JE, Pramstaller PP. Population isolates in South Tyrol and their value for genetic dissection of complex diseases Annals of Human Genetics. 70: 812-821. PMID 17044856 DOI: 10.1111/J.1469-1809.2006.00274.X |
0.329 |
|
| 2006 |
Schaid DJ, McDonnell SK, Zarfas KE, Cunningham JM, Hebbring S, Thibodeau SN, Eeles RA, Easton DF, Foulkes WD, Simard J, Giles GG, Hopper JL, Mahle L, Moller P, Badzioch M, ... ... Bailey-Wilson J, et al. Pooled genome linkage scan of aggressive prostate cancer: results from the International Consortium for Prostate Cancer Genetics. Human Genetics. 120: 471-85. PMID 16932970 DOI: 10.1007/s00439-006-0219-9 |
0.408 |
|
| 2006 |
Gillanders EM, Pearson JV, Sorant AJ, Trent JM, O'Connell JR, Bailey-Wilson JE. The value of molecular haplotypes in a family-based linkage study. American Journal of Human Genetics. 79: 458-68. PMID 16909384 DOI: 10.1086/506626 |
0.668 |
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| 2006 |
Aben KK, Baglietto L, Baffoe-Bonnie A, Coebergh JW, Bailey-Wilson JE, Trink B, Verbeek AL, Schoenberg MP, Alfred Witjes J, Kiemeney LA. Segregation analysis of urothelial cell carcinoma. European Journal of Cancer (Oxford, England : 1990). 42: 1428-33. PMID 16737809 DOI: 10.1016/J.Ejca.2005.07.039 |
0.416 |
|
| 2006 |
Doan BQ, Sorant AJ, Frangakis CE, Bailey-Wilson JE, Shugart YY. Covariate-based linkage analysis: application of a propensity score as the single covariate consistently improves power to detect linkage. European Journal of Human Genetics : Ejhg. 14: 1018-26. PMID 16736037 DOI: 10.1038/Sj.Ejhg.5201650 |
0.389 |
|
| 2006 |
Panhuysen CI, Karban A, Knodle Manning A, Bayless TM, Duerr RH, Bailey-Wilson JE, Epstein EH, Brant SR. Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree. Human Genetics. 120: 31-41. PMID 16733713 DOI: 10.1007/S00439-006-0163-8 |
0.434 |
|
| 2006 |
Mandal DM, Sorant AJ, Atwood LD, Wilson AF, Bailey-Wilson JE. Allele frequency misspecification: effect on power and Type I error of model-dependent linkage analysis of quantitative traits under random ascertainment. Bmc Genetics. 7: 21. PMID 16618369 DOI: 10.1186/1471-2156-7-21 |
0.34 |
|
| 2006 |
Marroni F, Pastrello C, Benatti P, Torrini M, Barana D, Cordisco EL, Viel A, Mareni C, Oliani C, Genuardi M, Bailey-Wilson JE, Ponz de Leon M, Presciuttini S. A genetic model for determining MSH2 and MLH1 carrier probabilities based on family history and tumor microsatellite instability Clinical Genetics. 69: 254-262. PMID 16542391 DOI: 10.1111/J.1399-0004.2006.00577.X |
0.376 |
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| 2006 |
Wojciechowski R, Moy C, Ciner E, Ibay G, Reider L, Bailey-Wilson JE, Stambolian D. Genomewide scan in Ashkenazi Jewish families demonstrates evidence of linkage of ocular refraction to a QTL on chromosome 1p36. Human Genetics. 119: 389-99. PMID 16501916 DOI: 10.1007/S00439-006-0153-X |
0.473 |
|
| 2006 |
Mononen N, Seppälä EH, Duggal P, Autio V, Ikonen T, Ellonen P, Saharinen J, Saarela J, Vihinen M, Tammela TL, Kallioniemi O, Bailey-Wilson JE, Schleutker J. Profiling genetic variation along the androgen biosynthesis and metabolism pathways implicates several single nucleotide polymorphisms and their combinations as prostate cancer risk factors. Cancer Research. 66: 743-7. PMID 16424004 DOI: 10.1158/0008-5472.Can-05-1723 |
0.45 |
|
| 2006 |
Chang BL, Lange EM, Dimitrov L, Valis CJ, Gillanders EM, Lange LA, Wiley KE, Isaacs SD, Wiklund F, Baffoe-Bonnie A, Langefeld CD, Zheng SL, Matikainen MP, Ikonen T, Fredriksson H, ... ... Bailey-Wilson JE, et al. Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effect. Human Genetics. 118: 716-24. PMID 16328469 DOI: 10.1007/S00439-005-0099-4 |
0.698 |
|
| 2006 |
Kittles RA, Baffoe-Bonnie AB, Moses TY, Robbins CM, Ahaghotu C, Huusko P, Pettaway C, Vijayakumar S, Bennett J, Hoke G, Mason T, Weinrich S, Trent JM, Collins FS, Mousses S, ... Bailey-Wilson J, et al. A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history. Journal of Medical Genetics. 43: 507-11. PMID 16155194 DOI: 10.1136/Jmg.2005.035790 |
0.437 |
|
| 2006 |
Pakkanen SK, Baffoe-Bonnie A, Koivisto P, Matikainen MP, Tammela TLJ, Ou L, Bailey-Wilson JE, Schleutker J. 240: Segregation Analysis of 1,546 Families with Prostate Cancer in Finland The Journal of Urology. 175: 80-80. DOI: 10.1016/S0022-5347(18)32507-2 |
0.434 |
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| 2005 |
Marroni F, Toni C, Pennato B, Tsai YY, Duggal P, Bailey-Wilson JE, Presciuttini S. Haplotypic structure of the X chromosome in the COGA population sample and the quality of its reconstruction by extant software packages. Bmc Genetics. 6: S77. PMID 16451691 DOI: 10.1186/1471-2156-6-S1-S77 |
0.362 |
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| 2005 |
Duggal P, Gillanders EM, Mathias RA, Ibay GP, Klein AP, Baffoe-Bonnie AB, Ou L, Dusenberry IP, Tsai YY, Chines PS, Doan BQ, Bailey-Wilson JE. Identification of tag single-nucleotide polymorphisms in regions with varying linkage disequilibrium. Bmc Genetics. 6: S73. PMID 16451687 DOI: 10.1186/1471-2156-6-S1-S73 |
0.641 |
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| 2005 |
Doan BQ, Frangakis CE, Shugart YY, Bailey-Wilson JE. Application of the propensity score in a covariate-based linkage analysis of the Collaborative Study on the Genetics of Alcoholism. Bmc Genetics. 6: S33. PMID 16451643 DOI: 10.1186/1471-2156-6-S1-S33 |
0.392 |
|
| 2005 |
Klein AP, Tsai YY, Duggal P, Gillanders EM, Barnhart M, Mathias RA, Dusenberry IP, Turiff A, Chines PS, Goldstein J, Wojciechowski R, Hening W, Pugh EW, Bailey-Wilson JE. Investigation of altering single-nucleotide polymorphism density on the power to detect trait loci and frequency of false positive in nonparametric linkage analyses of qualitative traits. Bmc Genetics. 6: S20. PMID 16451629 DOI: 10.1186/1471-2156-6-S1-S20 |
0.636 |
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| 2005 |
Bailey-Wilson JE, Almasy L, de Andrade M, Bailey J, Bickeböller H, Cordell HJ, Daw EW, Goldin L, Goode EL, Gray-McGuire C, Hening W, Jarvik G, Maher BS, Mendell N, Paterson AD, et al. Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans. Bmc Genetics. 6: S1. PMID 16451554 DOI: 10.1186/1471-2156-6-S1-S1 |
0.395 |
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| 2005 |
Beckmann L, Ziegler A, Duggal P, Bailey-Wilson JE. Haplotypes and haplotype-tagging single-nucleotide polymorphism: presentation Group 8 of Genetic Analysis Workshop 14. Genetic Epidemiology. 29: S59-71. PMID 16342175 DOI: 10.1002/Gepi.20111 |
0.428 |
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| 2005 |
Mathias RA, Beaty TH, Bailey-Wilson JE, Bickel C, Stockton ML, Barnes KC. Inheritance of total serum IgE in the isolated Tangier Island population from Virginia: Complexities associated with genealogical depth of pedigrees in segregation analyses Human Heredity. 59: 228-238. PMID 16093728 DOI: 10.1159/000087123 |
0.392 |
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| 2005 |
Stambolian D, Ciner EB, Reider LC, Moy C, Dana D, Owens R, Schlifka M, Holmes T, Ibay G, Bailey-Wilson JE. Genome-wide scan for myopia in the Old Order Amish. American Journal of Ophthalmology. 140: 469-76. PMID 16084785 DOI: 10.1016/J.Ajo.2005.04.014 |
0.416 |
|
| 2005 |
Xu J, Dimitrov L, Chang BL, Adams TS, Turner AR, Meyers DA, Eeles RA, Easton DF, Foulkes WD, Simard J, Giles GG, Hopper JL, Mahle L, Moller P, Bishop T, ... ... Bailey-Wilson J, et al. A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics. American Journal of Human Genetics. 77: 219-29. PMID 15988677 DOI: 10.1086/432377 |
0.522 |
|
| 2005 |
Baffoe-Bonnie AB, Smith JR, Stephan DA, Schleutker J, Carpten JD, Kainu T, Gillanders EM, Matikainen M, Teslovich TM, Tammela T, Sood R, Balshem AM, Scarborough SD, Xu J, Isaacs WB, ... ... Bailey-Wilson JE, et al. A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region. Human Genetics. 117: 307-16. PMID 15906096 DOI: 10.1007/S00439-005-1306-Z |
0.703 |
|
| 2005 |
Klein AP, Duggal P, Lee KE, O'Neill JA, Klein R, Bailey-Wilson JE, Klein BE. Polygenic effects and cigarette smoking account for a portion of the familial aggregation of nuclear sclerosis. American Journal of Epidemiology. 161: 707-13. PMID 15800262 DOI: 10.1093/Aje/Kwi102 |
0.338 |
|
| 2005 |
Duggal P, Klein AP, Lee KE, Iyengar SK, Klein R, Bailey-Wilson JE, Klein BE. A genetic contribution to intraocular pressure: the beaver dam eye study. Investigative Ophthalmology & Visual Science. 46: 555-60. PMID 15671282 DOI: 10.1167/Iovs.04-0729 |
0.427 |
|
| 2005 |
Klein AP, Duggal P, Lee KE, Klein R, Bailey-Wilson JE, Klein BE. Support for polygenic influences on ocular refractive error. Investigative Ophthalmology & Visual Science. 46: 442-6. PMID 15671267 DOI: 10.1167/Iovs.04-0794 |
0.412 |
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| 2005 |
Rökman A, Baffoe-Bonnie AB, Gillanders E, Fredriksson H, Autio V, Ikonen T, Gibbs KD, Jones M, Gildea D, Freas-Lutz D, Markey C, Matikainen MP, Koivisto PA, Tammela TL, Kallioniemi OP, ... ... Bailey-Wilson JE, et al. Hereditary prostate cancer in Finland: fine-mapping validates 3p26 as a major predisposition locus. Human Genetics. 116: 43-50. PMID 15549392 DOI: 10.1007/S00439-004-1214-7 |
0.72 |
|
| 2005 |
Baffoe-Bonnie AB, Smith JR, Stephan DA, Schleutker J, Carpten JD, Kainu T, Gillanders EM, Matikainen M, Teslovich TM, Tammela T, Sood R, Balshem AM, Scarborough SD, Xu J, Isaacs WB, ... ... Bailey-Wilson JE, et al. A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region Human Genetics. 118: 307-307. DOI: 10.1007/S00439-005-0050-8 |
0.664 |
|
| 2005 |
Bailey-Wilson JE, Almasy L, Edenberg H, Greenberg DA, Hansen MS, Kennedy GC, Thomas D, W. Pugh E, MacCluer JW. Genetic Analysis Workshop 14: Introduction to Workshop Summaries Genetic Epidemiology. 29: S1-S6. DOI: 10.1002/Gepi.20105 |
0.43 |
|
| 2004 |
Palacio JD, Castellanos FX, Pineda DA, Lopera F, Arcos-Burgos M, Quiroz YT, Henao GC, Puerta IC, RamÃrez DL, Rapoport JL, Bailey-Wilson J, Berg K, Muenke M. Attention-deficit/hyperactivity disorder and comorbidities in 18 Paisa Colombian multigenerational families. Journal of the American Academy of Child and Adolescent Psychiatry. 43: 1506-15. PMID 15564820 DOI: 10.1097/01.Chi.0000142279.79805.Dc |
0.322 |
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| 2004 |
Arcos-Burgos M, Castellanos FX, Pineda D, Lopera F, Palacio JD, Palacio LG, Rapoport JL, Berg K, Bailey-Wilson JE, Muenke M. Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11. American Journal of Human Genetics. 75: 998-1014. PMID 15497111 DOI: 10.1086/426154 |
0.407 |
|
| 2004 |
Gillanders EM, Masiello A, Gildea D, Umayam L, Duggal P, Jones MP, Klein AP, Freas-Lutz D, Ibay G, Trout K, Wolfsberg TG, Trent JM, Bailey-Wilson JE, Baxevanis AD. GeneLink: a database to facilitate genetic studies of complex traits. Bmc Genomics. 5: 81. PMID 15491493 DOI: 10.1186/1471-2164-5-81 |
0.652 |
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| 2004 |
Marroni F, Aretini P, D'Andre E, Caligo MA, Cortesi L, Viel A, Ricevuto E, Montagna M, Cipollini G, Federico M, Santarosa M, Marchetti P, Bailey-Wilson JE, Bevilacqua G, Parmigiani G, et al. Penetrances of breast and ovarian cancer in a large series of families tested for BRCA1/2 mutations European Journal of Human Genetics. 12: 899-906. PMID 15340362 DOI: 10.1038/Sj.Ejhg.5201256 |
0.39 |
|
| 2004 |
Gillanders EM, Xu J, Chang BL, Lange EM, Wiklund F, Bailey-Wilson JE, Baffoe-Bonnie A, Jones M, Gildea D, Riedesel E, Albertus J, Isaacs SD, Wiley KE, Mohai CE, Matikainen MP, et al. Combined genome-wide scan for prostate cancer susceptibility genes. Journal of the National Cancer Institute. 96: 1240-7. PMID 15316059 DOI: 10.1093/Jnci/Djh228 |
0.679 |
|
| 2004 |
Stambolian D, Ibay G, Reider L, Dana D, Moy C, Schlifka M, Holmes T, Ciner E, Bailey-Wilson JE. Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12. American Journal of Human Genetics. 75: 448-59. PMID 15273935 DOI: 10.1086/423789 |
0.504 |
|
| 2004 |
Bailey-Wilson JE, Amos CI, Pinney SM, Petersen GM, de Andrade M, Wiest JS, Fain P, Schwartz AG, You M, Franklin W, Klein C, Gazdar A, Rothschild H, Mandal D, Coons T, et al. A major lung cancer susceptibility locus maps to chromosome 6q23-25. American Journal of Human Genetics. 75: 460-74. PMID 15272417 DOI: 10.1086/423857 |
0.465 |
|
| 2004 |
Marazita ML, Murray JC, Lidral AC, Arcos-Burgos M, Cooper ME, Goldstein T, Maher BS, Daack-Hirsch S, Schultz R, Mansilla MA, Field LL, Liu YE, Prescott N, Malcolm S, Winter R, ... ... Bailey-Wilson JE, et al. Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35. American Journal of Human Genetics. 75: 161-73. PMID 15185170 DOI: 10.1086/422475 |
0.452 |
|
| 2004 |
Ahaghotu C, Baffoe-Bonnie A, Kittles R, Pettaway C, Powell I, Royal C, Wang H, Vijayakumar S, Bennett J, Hoke G, Mason T, Bailey-Wilson J, Boykin W, Berg K, Carpten J, et al. Clinical characteristics of African-American men with heriditary prostate cancer: The AAHPC study Prostate Cancer and Prostatic Diseases. 7: 165-169. PMID 15175665 DOI: 10.1038/Sj.Pcan.4500719 |
0.425 |
|
| 2004 |
Arcos-Burgos M, Castellanos FX, Konecki D, Lopera F, Pineda D, Palacio JD, Rapoport JL, Berg K, Bailey-Wilson J, Muenke M. Pedigree disequilibrium test (PDT) replicates association and linkage between DRD4 and ADHD in multigenerational and extended pedigrees from a genetic isolate. Molecular Psychiatry. 9: 252-9. PMID 15094785 DOI: 10.1038/Sj.Mp.4001396 |
0.373 |
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| 2004 |
Marroni F, Aretini P, D'Andrea E, Caligo MA, Cortesi L, Viel A, Ricevuto E, Montagna M, Cipollini G, Ferrari S, Santarosa M, Bisegna R, Bailey-Wilson JE, Bevilacqua G, Parmigiani G, et al. Evaluation of widely used models for predicting BRCA1 and BRCA2 mutations Journal of Medical Genetics. 41: 278-285. PMID 15060102 DOI: 10.1136/Jmg.2003.013623 |
0.37 |
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| 2004 |
Karban AS, Okazaki T, Panhuysen CI, Gallegos T, Potter JJ, Bailey-Wilson JE, Silverberg MS, Duerr RH, Cho JH, Gregersen PK, Wu Y, Achkar JP, Dassopoulos T, Mezey E, Bayless TM, et al. Functional annotation of a novel NFKB1 promoter polymorphism that increases risk for ulcerative colitis. Human Molecular Genetics. 13: 35-45. PMID 14613970 DOI: 10.1093/Hmg/Ddh008 |
0.399 |
|
| 2004 |
Huusko P, Juo SH, Gillanders E, Sarantaus L, Kainu T, Vahteristo P, Allinen M, Jones M, Rapakko K, Eerola H, Markey C, Vehmanen P, Gildea D, Freas-Lutz D, Blomqvist C, ... ... Bailey-Wilson J, et al. Genome-wide scanning for linkage in Finnish breast cancer families. European Journal of Human Genetics : Ejhg. 12: 98-104. PMID 14560309 DOI: 10.1038/Sj.Ejhg.5201091 |
0.718 |
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| 2004 |
Huusko P, Juo SH, Gillanders E, Sarantaus L, Kainu T, Vahteristo P, Allinen M, Jones M, Rapakko K, Eerola H, Markey C, Vehmanen P, Gildea D, Freas-Lutz D, Blomqvist C, ... ... Bailey-Wilson J, et al. Erratum: Genome-wide scanning for linkage in Finnish breast cancer families European Journal of Human Genetics. 12: 256-256. DOI: 10.1038/Sj.Ejhg.5201140 |
0.668 |
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| 2003 |
Klein AP, Kovac I, Sorant AJ, Baffoe-Bonnie A, Doan BQ, Ibay G, Lockwood E, Mandal D, Santhosh L, Weissbecker K, Woo J, Zambelli-Weiner A, Zhang J, Naiman DQ, Malley J, ... Bailey-Wilson JE, et al. Importance sampling method of correction for multiple testing in affected sib-pair linkage analysis. Bmc Genetics. 4: S73. PMID 14975141 DOI: 10.1186/1471-2156-4-S1-S73 |
0.326 |
|
| 2003 |
Almasy L, Amos CI, Bailey-Wilson JE, Cantor RM, Jaquish CE, Martinez M, Neuman RJ, Olson JM, Palmer LJ, Rich SS, Spence MA, MacCluer JW. Genetic Analysis Workshop 13: Analysis of Longitudinal Family Data for Complex Diseases and Related Risk Factors Bmc Genetics. 4: 1-3. PMID 14975069 DOI: 10.1186/1471-2156-4-S1-S1 |
0.367 |
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| 2003 |
Schleutker J, Baffoe-Bonnie AB, Gillanders E, Kainu T, Jones MP, Freas-Lutz D, Markey C, Gildea D, Riedesel E, Albertus J, Gibbs KD, Matikainen M, Koivisto PA, Tammela T, Bailey-Wilson JE, et al. Genome-wide scan for linkage in finnish hereditary prostate cancer (HPC) families identifies novel susceptibility loci at 11q14 and 3p25-26. The Prostate. 57: 280-9. PMID 14601024 DOI: 10.1002/Pros.10302 |
0.71 |
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| 2003 |
Wyszynski DF, Albacha-Hejazi H, Aldirani M, Hammod M, Shkair H, Karam A, Alashkar J, Holmes TN, Pugh EW, Doheny KF, McIntosh I, Beaty TH, Bailey-Wilson JE. A genome-wide scan for loci predisposing to non-syndromic cleft lip with or without cleft palate in two large Syrian families. American Journal of Medical Genetics. Part A. 123: 140-7. PMID 14598337 DOI: 10.1002/Ajmg.A.20283 |
0.442 |
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| 2003 |
Zeiger JS, Hetmanski JB, Beaty TH, VanderKolk CA, Wyszynski DF, Bailey-Wilson JE, de Luna RO, Perandones C, Tolarova MM, Mosby T, Bennun R, Segovia M, Calda P, Pugh EW, Doheny K, et al. Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2. European Journal of Human Genetics : Ejhg. 11: 835-9. PMID 14571267 DOI: 10.1038/Sj.Ejhg.5201052 |
0.445 |
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| 2003 |
Gillanders E, Juo SH, Holland EA, Jones M, Nancarrow D, Freas-Lutz D, Sood R, Park N, Faruque M, Markey C, Kefford RF, Palmer J, Bergman W, Bishop DT, Tucker MA, ... ... Bailey-Wilson JE, et al. Localization of a novel melanoma susceptibility locus to 1p22. American Journal of Human Genetics. 73: 301-13. PMID 12844286 DOI: 10.1086/377140 |
0.681 |
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| 2003 |
Malley JD, Redner RA, Severini TA, Badner JA, Pajevic S, Bailey-Wilson JE. Estimation of linkage and association from Allele transmission data Biometrical Journal. 45: 349-366. DOI: 10.1002/Bimj.200390017 |
0.357 |
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| 2002 |
Malley JD, Naiman DQ, Bailey-Wilson JE. A comprehensive method for genome scans Human Heredity. 54: 174-185. PMID 12771550 DOI: 10.1159/000070663 |
0.318 |
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| 2002 |
Presciuttini S, Toni C, Tempestini E, Verdiani S, Casarino L, Spinetti I, De Stefano F, Domenici R, Bailey-Wilson JE. Inferring relationships between pairs of individuals from locus heterozygosities Bmc Genetics [Electronic Resource]. 3: 23. PMID 12441003 DOI: 10.1186/1471-2156-3-23 |
0.347 |
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| 2002 |
Carpten JD, Robbins CM, Villablanca A, Forsberg L, Presciuttini S, Bailey-Wilson J, Simonds WF, Gillanders EM, Kennedy AM, Chen JD, Agarwal SK, Sood R, Jones MP, Moses TY, Haven C, et al. HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome. Nature Genetics. 32: 676-80. PMID 12434154 DOI: 10.1038/Ng1048 |
0.63 |
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| 2002 |
Baffoe-Bonnie AB, Kiemeney LALM, Beaty TH, Bailey-Wilson JE, Schnell AH, Sigvaldason H, Ólafsdóttir G, Tryggvadóttir L, Tulinius H. Segregation analysis of 389 Icelandic pedigrees with breast and prostate cancer Genetic Epidemiology. 23: 349-363. PMID 12432503 DOI: 10.1002/Gepi.10188 |
0.415 |
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| 2002 |
Anderson E, Berkovic S, Dulac O, Gardiner M, Jain S, Laue Friis M, Lindhout D, Noebels J, Ottman R, Scaramelli A, Serratosa J, Steinlein O, Avanzini G, Bailey-Wilson J, Cardon L, et al. ILAE genetics commission conference report: molecular analysis of complex genetic epilepsies. Epilepsia. 43: 1262-7. PMID 12366744 DOI: 10.1046/J.1528-1157.2002.29502.X |
0.332 |
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| 2002 |
Xu J, Zheng SL, Komiya A, Mychaleckyj JC, Isaacs SD, Hu JJ, Sterling D, Lange EM, Hawkins GA, Turner A, Ewing CM, Faith DA, Johnson JR, Suzuki H, Bujnovszky P, ... ... Bailey-Wilson JE, et al. Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk. Nature Genetics. 32: 321-5. PMID 12244320 DOI: 10.1038/Ng994 |
0.449 |
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| 2002 |
Klein AP, Beaty TH, Bailey-Wilson JE, Brune KA, Hruban RH, Petersen GM. Evidence for a major gene influencing risk of pancreatic cancer Genetic Epidemiology. 23: 133-149. PMID 12214307 DOI: 10.1002/Gepi.1102 |
0.409 |
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| 2002 |
Smith ACM, Groptnan AL, Bailey-Wilson JE, Goker-Alpan O, Elsea SH, Blancato J, Lupski JR, Potocki L. Hypercholesterolemia in children with Smith-Magenis syndrome: Del (17)(p11.2p11.2) Genetics in Medicine. 4: 118-125. PMID 12180145 DOI: 10.1097/00125817-200205000-00004 |
0.301 |
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| 2002 |
Arcos-Burgos M, Castellanos FX, Lopera F, Pineda D, Palacio JD, Garcia M, Henao GC, Palacio LG, Berg K, Bailey-Wilson JE, Muenke M. Attention-deficit/hyperactivity disorder (ADHD): feasibility of linkage analysis in a genetic isolate using extended and multigenerational pedigrees. Clinical Genetics. 61: 335-43. PMID 12081716 DOI: 10.1034/J.1399-0004.2002.610503.X |
0.417 |
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| 2002 |
Ho GY, Knapp M, Freije D, Nelson WG, Smith JR, Carpten JD, Bailey-Wilson JE, Beaty TH, Petersen G, Xu J, Kamensky V, Walsh PC, Isaacs WB. Transmission/disequilibrium tests of androgen receptor and glutathione S-transferase pi variants in prostate cancer families. International Journal of Cancer. Journal International Du Cancer. 98: 938-42. PMID 11948476 DOI: 10.1002/Ijc.10290 |
0.504 |
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| 2002 |
Rökman A, Ikonen T, Seppälä EH, Nupponen N, Autio V, Mononen N, Bailey-Wilson J, Trent J, Carpten J, Matikainen MP, Koivisto PA, Tammela TL, Kallioniemi OP, Schleutker J. Germline alterations of the RNASEL gene, a candidate HPC1 gene at 1q25, in patients and families with prostate cancer. American Journal of Human Genetics. 70: 1299-304. PMID 11941539 DOI: 10.1086/340450 |
0.48 |
|
| 2002 |
Rozenblum E, Vahteristo P, Sandberg T, Bergthorsson JT, Syrjakoski K, Weaver D, Haraldsson K, Johannsdottir HK, Vehmanen P, Nigam S, Golberger N, Robbins C, Pak E, Dutra A, Gillander E, ... ... Bailey-Wilson J, et al. A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes. Human Genetics. 110: 111-21. PMID 11935316 DOI: 10.1007/S00439-001-0646-6 |
0.447 |
|
| 2002 |
Stephan DA, Howell GR, Teslovich TM, Coffey AJ, Smith L, Bailey-Wilson JE, Malechek L, Gildea D, Smith JR, Gillanders EM, Schleutker J, Hu P, Steingruber HE, Dhami P, Robbins CM, et al. Physical and transcript map of the hereditary prostate cancer region at xq27. Genomics. 79: 41-50. PMID 11827456 DOI: 10.1006/Geno.2001.6681 |
0.641 |
|
| 2002 |
Carpten J, Nupponen N, Isaacs S, Sood R, Robbins C, Xu J, Faruque M, Moses T, Ewing C, Gillanders E, Hu P, Bujnovszky P, Makalowska I, Baffoe-Bonnie A, Faith D, ... ... Bailey-Wilson J, et al. Germline mutations in the ribonuclease L gene in families showing linkage with HPC1. Nature Genetics. 30: 181-4. PMID 11799394 DOI: 10.1038/Ng823 |
0.681 |
|
| 2002 |
Matikainen M, Schleutker J, Gillanders E, Baffoe-Bonnie A, Jones MP, Kainu T, Markey C, Koivisto P, Tammela T, Bailey-Wilson J, Trent J, Kallioniemi O. Novel region of interest in chromosome 11 and other putative regions identified in a genome-wide scan in finnish hereditary prostate cancer families European Urology Supplements. 1: 8. DOI: 10.1016/S1569-9056(02)80020-3 |
0.693 |
|
| 2001 |
Bailey-Wilson JE, Sorant AJ, Malley JD, Presciuttini S, Redner RA, Severini TA, Badner JA, Pajevic S, Jufer R, Baffoe-Bonnie A, Kao L, Doan BQ, Goldstein JL, Holmes TN, Behneman D, et al. Comparison of novel and existing methods for detection of linkage disequilibrium using parent-child trios in the GAW12 genetic isolate simulated data. Genetic Epidemiology. 21: S378-83. PMID 11793703 DOI: 10.1002/Gepi.2001.21.S1.S378 |
0.416 |
|
| 2001 |
Mandal DM, Wilson AF, Bailey-Wilson JE. Effects of misspecification of allele frequencies on the power of Haseman-Elston sib-pair linkage method for quantitative traits American Journal of Medical Genetics. 103: 308-313. PMID 11746011 DOI: 10.1002/Ajmg.1566 |
0.379 |
|
| 2001 |
Cavanaugh JA, Bryce ME, Stanford PM, Pavli P, Vermeire S, Peeters M, Vlietinck R, Rutgeerts P, Rioux JD, Silverberg MS, Steinhart AH, Siminovitch KA, Hugot JP, Lesage S, Zouali H, ... ... Bailey-Wilson JE, et al. International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16 American Journal of Human Genetics. 68: 1165-1171. PMID 11309682 DOI: 10.1086/320119 |
0.301 |
|
| 2001 |
Xu J, Zheng SL, Carpten JD, Nupponen NN, Robbins CM, Mestre J, Moses TY, Faith DA, Kelly BD, Isaacs SD, Wiley KE, Ewing CM, Bujnovszky P, Chang B, Bailey-Wilson J, et al. Evaluation of linkage and association of HPC2/ELAC2 in patients with familial or sporadic prostate cancer. American Journal of Human Genetics. 68: 901-11. PMID 11254448 DOI: 10.1086/319513 |
0.491 |
|
| 2001 |
Verhage BA, Baffoe-Bonnie AB, Baglietto L, Smith DS, Bailey-Wilson JE, Beaty TH, Catalona WJ, Kiemeney LA. Autosomal dominant inheritance of prostate cancer: a confirmatory study. Urology. 57: 97-101. PMID 11164151 DOI: 10.1016/S0090-4295(00)00891-8 |
0.416 |
|
| 2001 |
Karban AS, Panhuysen CI, Bailey-Wilson JE, Friedman Y, Ravenhill G, Cho JH, Duerr RH, Bayless TM, Epstein EH, Brant SR. A genome wide screen in an unusually large inflammatory bowel disease pedigree: Suggestive evidence for linkage on chromosomes 18p, 7p and 15q; No evidence for IBD1 or IBD2 loci Gastroenterology. 120: A37. DOI: 10.1016/S0016-5085(08)80180-1 |
0.351 |
|
| 2000 |
Royal C, Baffoe-Bonnie A, Kittles R, Powell I, Bennett J, Hoke G, Pettaway C, Weinrich S, Vijayakumar S, Ahaghotu C, Mason T, Johnson E, Obeikwe M, Simpson C, Mejia R, ... ... Bailey-Wilson J, et al. Recruitment experience in the first phase of the African American Hereditary Prostate Cancer (AAHPC) study Annals of Epidemiology. 10. PMID 11189095 DOI: 10.1016/S1047-2797(00)00194-0 |
0.457 |
|
| 2000 |
Bergthorsson JT, Johannesdottir G, Arason A, Benediktsdottir KR, Agnarsson BA, Bailey-Wilson JE, Gillanders E, Smith J, Trent J, Barkardottir RB. Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancer. Human Genetics. 107: 372-5. PMID 11129338 DOI: 10.1007/S004390000384 |
0.723 |
|
| 2000 |
Bailey-Wilson J, Baron J, Cawthon R, Christian JC, Corder EH, Franceschi C, Kestenbaum B, Kruglyak L, Lauderdale DS, Lubitz J, Martin GM, McClearn GE, McGue M, Miles T, Mineau G, et al. Genetic epidemiologic studies on age-specified traits American Journal of Epidemiology. 152: 1003-1008. PMID 11117608 DOI: 10.1093/Aje/152.11.1003 |
0.312 |
|
| 2000 |
Kainu T, Juo SHH, Desper R, Schäffer AA, Gillanders E, Rozenblum E, Freas-Lutz D, Weaver D, Stephan D, Bailey-Wilson J, Kallioniemi OP, Tirkkonen M, Syrjäkoski K, Kuukasjärvi T, Koivisto P, et al. Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus Proceedings of the National Academy of Sciences of the United States of America. 97: 9603-9608. PMID 10944226 DOI: 10.1073/Pnas.97.17.9603 |
0.676 |
|
| 2000 |
Zhang W, Bailey-Wilson JE, Li W, Wang X, Zhang C, Mao X, Liu Z, Zhou C, Wu M. Segregation analysis of esophageal cancer in a moderately high-incidence area of northern China American Journal of Human Genetics. 67: 110-119. PMID 10841811 DOI: 10.1086/302970 |
0.38 |
|
| 2000 |
Mandal DM, Wilson AF, Elston RC, Weissbecker K, Keats BJ, Bailey-Wilson JE. Effects of misspecification of allele frequencies on the type I error rate of model-free linkage analysis Human Heredity. 50: 126-132. PMID 10799971 DOI: 10.1159/000022900 |
0.347 |
|
| 2000 |
Ho GYF, Bailey-Wilson JE. The transmission/disequilibrium test for linkage on the X chromosome American Journal of Human Genetics. 66: 1158-1160. PMID 10712228 DOI: 10.1086/302822 |
0.38 |
|
| 1999 |
Appukuttan B, Gillanders E, Juo SH, Freas-Lutz D, Ott S, Sood R, Van Auken A, Bailey-Wilson J, Wang X, Patel RJ, Robbins CM, Chung M, Annett G, Weinberg K, Borchert MS, et al. Localization of a gene for Duane retraction syndrome to chromosome 2q31. American Journal of Human Genetics. 65: 1639-46. PMID 10577917 DOI: 10.1086/302656 |
0.669 |
|
| 1999 |
Pollin TI, Dobyns WB, Crowe CA, Ledbetter DH, Bailey-Wilson JE, Smith ACM. Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in chromosome 17p13.3 American Journal of Medical Genetics. 85: 369-375. PMID 10398263 DOI: 10.1002/(Sici)1096-8628(19990806)85:4<369::Aid-Ajmg13>3.0.Co;2-L |
0.327 |
|
| 1999 |
Juo SHH, Wyszynski DF, Beaty TH, Huang HY, Bailey-Wilson JE. Mild association between the A/G polymorphism in the promoter of the apolipoprotein A-I gene and apolipoprotein A-I levels: A meta-analysis American Journal of Medical Genetics. 82: 235-241. PMID 10215547 DOI: 10.1002/(Sici)1096-8628(19990129)82:3<235::Aid-Ajmg8>3.0.Co;2-H |
0.358 |
|
| 1999 |
Stephan DA, Gillanders E, Vanderveen D, Freas-Lutz D, Wistow G, Baxevanis AD, Robbins CM, VanAuken A, Quesenberry MI, Bailey-Wilson J, Juo SH, Trent JM, Smith L, Brownstein MJ. Progressive juvenile-onset punctate cataracts caused by mutation of the gammaD-crystallin gene. Proceedings of the National Academy of Sciences of the United States of America. 96: 1008-12. PMID 9927684 DOI: 10.1073/Pnas.96.3.1008 |
0.634 |
|
| 1999 |
Matikainen MP, Schleutker J, Koivisto PA, Tammela T, Xu J, Isaacs WB, Smith JR, Carpten JD, Stephan DA, Bailey-Wilson JE, Trent JM, Kallioniemi O. Genetic Epidemiology Of Hereditary Prostate Cancer In Finland: Discovery Of Novel Susceptibility Loci The Journal of Urology. 54. DOI: 10.1097/00005392-199904010-00220 |
0.444 |
|
| 1998 |
Wyszynski DF, Zeiger J, Tilli MT, Bailey-Wilson JE, Beaty TH. Survey of genetic counselors and clinical geneticists regarding recurrence risks for families with nonsyndromic cleft lip with or without cleft palate American Journal of Medical Genetics. 79: 184-190. PMID 9788558 DOI: 10.1002/(Sici)1096-8628(19980923)79:3<184::Aid-Ajmg6>3.0.Co;2-N |
0.396 |
|
| 1998 |
Xu J, Meyers D, Freije D, Isaacs S, Wiley K, Nusskern D, Ewing C, Wilkens E, Bujnovszky P, Bova GS, Walsh P, Isaacs W, Schleutker J, Matikainen M, Tammela T, ... ... Bailey-Wilson J, et al. Evidence for a prostate cancer susceptibility locus on the X chromosome. Nature Genetics. 20: 175-9. PMID 9771711 DOI: 10.1016/S0022-5347(01)61689-6 |
0.708 |
|
| 1998 |
Becker KG, Simon RM, Bailey-Wilson JE, Freidlin B, Biddison WE, McFarland HF, Trent JM. Clustering of non-major histocompatibility complex susceptibility candidate loci in human autoimmune diseases. Proceedings of the National Academy of Sciences of the United States of America. 95: 9979-84. PMID 9707586 DOI: 10.1073/Pnas.95.17.9979 |
0.321 |
|
| 1998 |
Aitken JF, Bailey-Wilson J, Green AC, MacLennan R, Martin NG. Segregation analysis of cutaneous melanoma in Queensland Genetic Epidemiology. 15: 391-401. PMID 9671988 DOI: 10.1002/(Sici)1098-2272(1998)15:4<391::Aid-Gepi5>3.0.Co;2-5 |
0.417 |
|
| 1997 |
Pugh EW, Jaquish CE, Sorant AJM, Doetsch JP, Bailey-Wilson JE, Wilson AF. Comparison of sib-pair and variance-components methods for genomic screening Genetic Epidemiology. 14: 867-872. PMID 9433592 DOI: 10.1002/(Sici)1098-2272(1997)14:6<867::Aid-Gepi51>3.0.Co;2-K |
0.33 |
|
| 1997 |
Wyszynski DF, Doetsch JP, Pugh EW, Bailey-Wilson JE. Comparison of selected methods used to analyze bipolar disorder Genetic Epidemiology. 14: 705-710. PMID 9433567 DOI: 10.1002/(Sici)1098-2272(1997)14:6<705::Aid-Gepi26>3.0.Co;2-T |
0.369 |
|
| 1997 |
Trent J, Smith J, Freije D, Carpten J, Gronberg H, Xu J, Isaacs S, Brownstein M, Bova G, Guo H, Bujnovszky P, Nusskern D, Damber J, Bergh A, Emanuelsson M, ... ... Bailey-Wilson J, et al. Identification of a major susceptibility locus for human prostate cancer Cancer Genetics and Cytogenetics. 98: 146. DOI: 10.1016/S0165-4608(97)90228-4 |
0.387 |
|
| 1996 |
Smith JR, Freije D, Carpten JD, Grönberg H, Xu J, Isaacs SD, Brownstein MJ, Bova GS, Guo H, Bujnovszky P, Nusskern DR, Damber JE, Bergh A, Emanuelsson M, Kallioniemi OP, ... ... Bailey-Wilson JE, et al. Major susceptibility locus for prostate cancer on chromosome 1 suggested by a genome-wide search. Science (New York, N.Y.). 274: 1371-4. PMID 8910276 DOI: 10.1126/Science.274.5291.1371 |
0.51 |
|
| 1995 |
Spence MA, Flodman PL, Sadovnick AD, Bailey-Wilson JE, Ameli H, Remick RA. Bipolar disorder: Evidence for a major locus American Journal of Medical Genetics - Neuropsychiatric Genetics. 60: 370-376. PMID 8546148 DOI: 10.1002/Ajmg.1320600505 |
0.337 |
|
| 1994 |
Sellers TA, Chen PL, Potter JD, Bailey-Wilson JE, Rothschild H, Elston RC. Segregation analysis of smoking-associated malignancies: Evidence for Mendelian inheritance American Journal of Medical Genetics. 52: 308-314. PMID 7810562 DOI: 10.1002/Ajmg.1320520311 |
0.302 |
|
| 1993 |
Dobin A, Kimberling WJ, Pettinger W, Bailey-Wilson JE, Shugart YY, Gabow P. Segregation analysis of autosomal dominant polycystic kidney disease Genetic Epidemiology. 10: 189-200. PMID 8349100 DOI: 10.1002/Gepi.1370100305 |
0.335 |
|
| 1993 |
Bailey-Wilson JE, Wilson AF, Bamba V. Linkage analysis in a large pedigree ascertained due to essential familial hypercholesterolemia Genetic Epidemiology. 10: 665-669. PMID 8314078 DOI: 10.1002/Gepi.1370100656 |
0.325 |
|
| 1993 |
Bailey-Wilson JE, Elston RC. The HGAR1 familial hypercholesterolemia pedigree Genetic Epidemiology. 10: 529-531. PMID 8314055 DOI: 10.1002/gepi.1370100633 |
0.328 |
|
| 1992 |
Bailey-Wilson JE, Dobbins TE. Sib-pair linkage analysis applied to pedigrees with melanoma and dysplastic nevi Cytogenetics and Cell Genetics. 59: 176-178. PMID 1737492 DOI: 10.1159/000133237 |
0.336 |
|
| 1992 |
Sellers TA, Bailey-Wilson JE, Potter JD, Rich SS, Rothschild H, Elston RC. Effect of cohort differences in smoking prevalence on models of lung cancer susceptibility Genetic Epidemiology. 9: 261-271. PMID 1398045 DOI: 10.1002/Gepi.1370090405 |
0.351 |
|
| 1990 |
Sellers TA, Bailey-Wilson JE, Elston RC, Wilson AF, Elston GZ, Ooi WL, Rothschild H. Evidence for mendelian inheritance in the pathogenesis of lung cancer. Journal of the National Cancer Institute. 82: 1272-9. PMID 2374177 DOI: 10.1093/Jnci/82.15.1272 |
0.365 |
|
| 1987 |
Sellers TA, Ooi WL, Elston RC, Chen VW, Bailey-Wilson JE, Rothschild H. Increased familial risk for non-lung cancer among relatives of lung cancer patients. American Journal of Epidemiology. 126: 237-46. PMID 3605052 DOI: 10.1093/Aje/126.2.237 |
0.43 |
|
| 1986 |
Wilson AF, Bailey-Wilson JE, Cleton FJ. Linkage analysis of Dutch families at high risk for breast cancer Genetic Epidemiology. 3: 87-92. PMID 3471674 DOI: 10.1002/Gepi.1370030714 |
0.481 |
|
| 1986 |
Ooi WL, Elston RC, Chen VW, Bailey-Wilson JE, Rothschild H. Increased familial risk for lung cancer. Journal of the National Cancer Institute. 76: 217-22. PMID 3456060 DOI: 10.1093/Jnci/76.2.217 |
0.342 |
|
| 1983 |
King MC, Go RC, Lynch HT, Elston RC, Terasaki PI, Petrakis NL, Rodgers GC, Lattanzio D, Bailey-Wilson J. Genetic epidemiology of breast cancer and associated cancers in high-risk families. II. Linkage analysis. Journal of the National Cancer Institute. 71: 463-7. PMID 6577221 DOI: 10.1093/Jnci/71.3.463 |
0.458 |
|
| 1983 |
Go RCP, King M, Bailey-Wilson J, Elston RC, Lynch HT. Genetic Epidemiology of Breast Cancer and Associated Cancers in High-Risk Families. I. Segregation Analysis Journal of the National Cancer Institute. 71: 455-461. DOI: 10.1093/Jnci/71.3.455 |
0.414 |
|
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