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Carole Ober - Publications

Affiliations: 
University of Chicago, Chicago, IL 
Website:
http://www.genes.uchicago.edu/fri/oberres.html

214 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Schoettler N, Hrusch CL, Blaine KM, Sperling AI, Ober C. Transcriptional programming and T cell receptor repertoires distinguish human lung and lymph node memory T cells. Communications Biology. 2: 411. PMID 31925217 DOI: 10.1038/s42003-019-0657-2  0.84
2019 Schoettler N, Hrusch CL, Blaine KM, Sperling AI, Ober C. Transcriptional programming and T cell receptor repertoires distinguish human lung and lymph node memory T cells. Communications Biology. 2: 411. PMID 31754641 DOI: 10.1038/s42003-019-0657-2  0.76
2018 Stein MM, Hrusch CL, Sperling AI, Ober C. Effects of an FcγRIIA polymorphism on leukocyte gene expression and cytokine responses to anti-CD3 and anti-CD28 antibodies. Genes and Immunity. PMID 29977032 DOI: 10.1038/S41435-018-0038-8  0.68
2018 Knowles DA, Burrows CK, Blischak JD, Patterson KM, Serie DJ, Norton N, Ober C, Pritchard JK, Gilad Y. Determining the genetic basis of anthracycline-cardiotoxicity by response QTL mapping in induced cardiomyocytes. Elife. 7. PMID 29737278 DOI: 10.7554/Elife.33480  0.44
2018 Knowles DA, Burrows CK, Blischak JD, Patterson KM, Serie DJ, Norton N, Ober C, Pritchard JK, Gilad Y. Author response: Determining the genetic basis of anthracycline-cardiotoxicity by molecular response QTL mapping in induced cardiomyocytes Elife. DOI: 10.7554/Elife.33480.050  0.44
2017 Montefiori L, Hernandez L, Zhang Z, Gilad Y, Ober C, Crawford G, Nobrega M, Jo Sakabe N. Reducing mitochondrial reads in ATAC-seq using CRISPR/Cas9. Scientific Reports. 7: 2451. PMID 28550296 DOI: 10.1038/S41598-017-02547-W  0.44
2017 Igartua C, Davenport ER, Gilad Y, Nicolae DL, Pinto J, Ober C. Host genetic variation in mucosal immunity pathways influences the upper airway microbiome. Microbiome. 5: 16. PMID 28143570 DOI: 10.1186/s40168-016-0227-5  0.44
2016 Papachristou C, Ober C, Abney M. A LASSO penalized regression approach for genome-wide association analyses using related individuals: application to the Genetic Analysis Workshop 19 simulated data. Bmc Proceedings. 10: 221-226. PMID 27980640 DOI: 10.1186/s12919-016-0034-9  0.52
2016 Nicodemus-Johnson J, Myers RA, Sakabe NJ, Sobreira DR, Hogarth DK, Naureckas ET, Sperling AI, Solway J, White SR, Nobrega MA, Nicolae DL, Gilad Y, Ober C. DNA methylation in lung cells is associated with asthma endotypes and genetic risk. Jci Insight. 1: e90151. PMID 27942592 DOI: 10.1172/Jci.Insight.90151  0.44
2016 Stein MM, Hrusch CL, Gozdz J, Igartua C, Pivniouk V, Murray SE, Ledford JG, Marques Dos Santos M, Anderson RL, Metwali N, Neilson JW, Maier RM, Gilbert JA, Holbreich M, Thorne PS, ... ... Ober C, et al. Innate Immunity and Asthma Risk in Amish and Hutterite Farm Children. The New England Journal of Medicine. 375: 411-21. PMID 27518660 DOI: 10.1056/Nejmoa1508749  1
2016 Burrows CK, Kosova G, Herman C, Patterson K, Hartmann KE, Velez Edwards DR, Stephenson MD, Lynch VJ, Ober C. Expression Quantitative Trait Locus Mapping Studies in Mid-secretory Phase Endometrial Cells Identifies HLA-F and TAP2 as Fecundability-Associated Genes. Plos Genetics. 12: e1005858. PMID 27447835 DOI: 10.1371/Journal.Pgen.1005858  1
2016 Goodrich JK, Davenport ER, Beaumont M, Jackson MA, Knight R, Ober C, Spector TD, Bell JT, Clark AG, Ley RE. Genetic Determinants of the Gut Microbiome in UK Twins. Cell Host & Microbe. 19: 731-43. PMID 27173935 DOI: 10.1016/J.Chom.2016.04.017  1
2016 Ober C. Asthma Genetics in the Post-GWAS Era. Annals of the American Thoracic Society. 13: S85-90. PMID 27027959 DOI: 10.1513/AnnalsATS.201507-459MG  1
2016 Igartua C, Davenport ER, Chupp GL, Elias JA, Gilad Y, Ober C, Pinto JM. Nasal Microbiome Composition Is Associated with Chitotriosidase (Chit1) Activity in Adult Hutterites. Annals of the American Thoracic Society. 13: S100-1. PMID 27027937 DOI: 10.1513/Annalsats.201508-521Mg  0.44
2016 Bønnelykke K, Ober C. Leveraging gene-environment interactions and endotypes for asthma gene discovery. The Journal of Allergy and Clinical Immunology. 137: 667-79. PMID 26947980 DOI: 10.1016/j.jaci.2016.01.006  1
2016 Cusanovich DA, Caliskan M, Billstrand C, Michelini K, Chavarria C, De Leon S, Mitrano A, Lewellyn N, Elias JA, Chupp GL, Lang RM, Shah SJ, DeCara JM, Gilad Y, Ober C. Integrated Analyses of Gene Expression and Genetic Association Studies in a Founder Population. Human Molecular Genetics. PMID 26931462 DOI: 10.1093/Hmg/Ddw061  0.44
2015 Davenport ER, Cusanovich DA, Michelini K, Barreiro LB, Ober C, Gilad Y. Genome-Wide Association Studies of the Human Gut Microbiota. Plos One. 10: e0140301. PMID 26528553 DOI: 10.1371/Journal.Pone.0140301  1
2015 Nicodemus-Johnson J, Naughton KA, Sudi J, Hogarth K, Naurekas ET, Nicolae DL, Sperling AI, Solway J, White SR, Ober C. Genome-wide Methylation Study Identifies an IL-13 Induced Epigenetic Signature in Asthmatic Airways. American Journal of Respiratory and Critical Care Medicine. PMID 26474238 DOI: 10.1164/Rccm.201506-1243Oc  1
2015 Sengupta S, Gulukota K, Zhu Y, Ober C, Naughton K, Wentworth-Sheilds W, Ji Y. Ultra-fast local-haplotype variant calling using paired-end DNA-sequencing data reveals somatic mosaicism in tumor and normal blood samples. Nucleic Acids Research. PMID 26420835 DOI: 10.1093/nar/gkv953  1
2015 Loisel DA, Du G, Ahluwalia TS, Tisler CJ, Evans MD, Myers RA, Gangnon RE, Møller EK, Bønnelykke K, Bisgaard H, Jackson DJ, Lemanske RF, Nicolae DL, Gern JE, Ober C. Genetic associations with viral respiratory illnesses and asthma control in children. Clinical and Experimental Allergy : Journal of the British Society For Allergy and Clinical Immunology. PMID 26399222 DOI: 10.1111/Cea.12642  1
2015 Levy BD, Noel PJ, Freemer MM, Cloutier MM, Georas SN, Jarjour NN, Ober C, Woodruff PG, Barnes KC, Bender BG, Camargo CA, Chupp GL, Denlinger LC, Fahy JV, Fitzpatrick AM, et al. Future Research Directions in Asthma: An NHLBI Working Group Report. American Journal of Respiratory and Critical Care Medicine. PMID 26305520 DOI: 10.1164/rccm.201505-0963WS  1
2015 Wheway G, Schmidts M, Mans DA, Szymanska K, Nguyen TT, Racher H, Phelps IG, Toedt G, Kennedy J, Wunderlich KA, Sorusch N, Abdelhamed ZA, Natarajan S, Herridge W, van Reeuwijk J, ... ... Ober C, et al. An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes. Nature Cell Biology. PMID 26167768 DOI: 10.1038/Ncb3201  1
2015 Kim KW, Myers RA, Lee JH, Igartua C, Lee KE, Kim YH, Kim EJ, Yoon D, Lee JS, Hirota T, Tamari M, Takahashi A, Kubo M, Choi JM, Kim KE, ... ... Ober C, et al. Genome-wide association study of recalcitrant atopic dermatitis in Korean children. The Journal of Allergy and Clinical Immunology. PMID 25935106 DOI: 10.1016/J.Jaci.2015.03.030  1
2015 Çal??kan M, Baker SW, Gilad Y, Ober C. Host genetic variation influences gene expression response to rhinovirus infection. Plos Genetics. 11: e1005111. PMID 25874939 DOI: 10.1371/Journal.Pgen.1005111  1
2015 Livne OE, Han L, Alkorta-Aranburu G, Wentworth-Sheilds W, Abney M, Ober C, Nicolae DL. PRIMAL: Fast and accurate pedigree-based imputation from sequence data in a founder population. Plos Computational Biology. 11: e1004139. PMID 25735005 DOI: 10.1371/Journal.Pcbi.1004139  1
2015 Igartua C, Myers RA, Mathias RA, Pino-Yanes M, Eng C, Graves PE, Levin AM, Del-Rio-Navarro BE, Jackson DJ, Livne OE, Rafaels N, Edlund CK, Yang JJ, Huntsman S, Salam MT, ... ... Ober C, et al. Ethnic-specific associations of rare and low-frequency DNA sequence variants with asthma. Nature Communications. 6: 5965. PMID 25591454 DOI: 10.1038/Ncomms6965  1
2015 Kosova G, Stephenson MD, Lynch VJ, Ober C. Evolutionary forward genomics reveals novel insights into the genes and pathways dysregulated in recurrent early pregnancy loss. Human Reproduction (Oxford, England). 30: 519-29. PMID 25586782 DOI: 10.1093/Humrep/Deu355  1
2015 Pino-Yanes M, Gignoux CR, Galanter JM, Levin AM, Campbell CD, Eng C, Huntsman S, Nishimura KK, Gourraud PA, Mohajeri K, O'Roak BJ, Hu D, Mathias RA, Nguyen EA, Roth LA, ... ... Ober C, et al. Genome-wide association study and admixture mapping reveal new loci associated with total IgE levels in Latinos. The Journal of Allergy and Clinical Immunology. 135: 1502-10. PMID 25488688 DOI: 10.1016/J.Jaci.2014.10.033  1
2015 Bouzigon E, Nadif R, Thompson EE, Concas MP, Kuldanek S, Du G, Brossard M, Lavielle N, Sarnowski C, Vaysse A, Dessen P, van der Valk RJ, Duijts L, Henderson AJ, Jaddoe VW, ... ... Ober C, et al. A common variant in RAB27A gene is associated with fractional exhaled nitric oxide levels in adults. Clinical and Experimental Allergy : Journal of the British Society For Allergy and Clinical Immunology. 45: 797-806. PMID 25431337 DOI: 10.1111/Cea.12461  1
2015 Loucks CM, Parboosingh JS, Shaheen R, Bernier FP, Mcleod DR, Seidahmed MZ, Puffenberger EG, Ober C, Hegele RA, Boycott KM, Alkuraya FS, Innes AM. Matching Two Independent Cohorts Validates DPH1 as a Gene Responsible for Autosomal Recessive Intellectual Disability with Short Stature, Craniofacial, and Ectodermal Anomalies Human Mutation. DOI: 10.1002/humu.22843  1
2014 Hansel NN, Paré PD, Rafaels N, Sin D, Sandford A, Daley D, Vergara C, Huang L, Elliott WM, Pascoe CD, Arsenault BA, Postma DS, Boezen HM, Bossé Y, van den Berge M, ... ... Ober C, et al. Genome Wide Association Study Identifies Novel Loci Associated with Airway Responsiveness in COPD. American Journal of Respiratory Cell and Molecular Biology. PMID 25514360 DOI: 10.1165/Rcmb.2014-0198Oc  1
2014 Çal??kan M, Pritchard JK, Ober C, Gilad Y. The effect of freeze-thaw cycles on gene expression levels in lymphoblastoid cell lines. Plos One. 9: e107166. PMID 25192014 DOI: 10.1371/Journal.Pone.0107166  1
2014 Campbell CD, Mohajeri K, Malig M, Hormozdiari F, Nelson B, Du G, Patterson KM, Eng C, Torgerson DG, Hu D, Herman C, Chong JX, Ko A, O'Roak BJ, Krumm N, ... ... Ober C, et al. Whole-genome sequencing of individuals from a founder population identifies candidate genes for asthma. Plos One. 9: e104396. PMID 25116239 DOI: 10.1371/Journal.Pone.0104396  1
2014 Bunyavanich S, Schadt EE, Himes BE, Lasky-Su J, Qiu W, Lazarus R, Ziniti JP, Cohain A, Linderman M, Torgerson DG, Eng CS, Pino-Yanes M, Padhukasahasram B, Yang JJ, Mathias RA, ... ... Ober C, et al. Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis. Bmc Medical Genomics. 7: 48. PMID 25085501 DOI: 10.1186/1755-8794-7-48  1
2014 Breton CV, Siegmund KD, Joubert BR, Wang X, Qui W, Carey V, Nystad W, Håberg SE, Ober C, Nicolae D, Barnes KC, Martinez F, Liu A, Lemanske R, Strunk R, et al. Prenatal tobacco smoke exposure is associated with childhood DNA CpG methylation. Plos One. 9: e99716. PMID 24964093 DOI: 10.1371/Journal.Pone.0099716  1
2014 Sharma S, Zhou X, Thibault DM, Himes BE, Liu A, Szefler SJ, Strunk R, Castro M, Hansel NN, Diette GB, Vonakis BM, Adkinson NF, Avila L, Soto-Quiros M, Barraza-Villareal A, ... ... Ober C, et al. A genome-wide survey of CD4(+) lymphocyte regulatory genetic variants identifies novel asthma genes. The Journal of Allergy and Clinical Immunology. 134: 1153-62. PMID 24934276 DOI: 10.1016/J.Jaci.2014.04.011  1
2014 Myers RA, Scott NM, Gauderman WJ, Qiu W, Mathias RA, Romieu I, Levin AM, Pino-Yanes M, Graves PE, Villarreal AB, Beaty TH, Carey VJ, Croteau-Chonka DC, del Rio Navarro B, Edlund C, ... ... Ober C, et al. Genome-wide interaction studies reveal sex-specific asthma risk alleles. Human Molecular Genetics. 23: 5251-9. PMID 24824216 DOI: 10.1093/Hmg/Ddu222  1
2014 Anderson RL, Murray K, Chong JX, Ouwenga R, Antillon M, Chen P, Diaz de Leon L, Swoboda KJ, Lester LA, Das S, Ober C, Waggoner DJ. Disclosure of genetic research results to members of a founder population. Journal of Genetic Counseling. 23: 984-91. PMID 24777552 DOI: 10.1007/S10897-014-9721-8  1
2014 Davenport ER, Mizrahi-Man O, Michelini K, Barreiro LB, Ober C, Gilad Y. Seasonal variation in human gut microbiome composition. Plos One. 9: e90731. PMID 24618913 DOI: 10.1371/journal.pone.0090731  1
2014 van der Valk RJ, Duijts L, Timpson NJ, Salam MT, Standl M, Curtin JA, Genuneit J, Kerhof M, Kreiner-Møller E, Cáceres A, Gref A, Liang LL, Taal HR, Bouzigon E, Demenais F, ... ... Ober C, et al. Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants. The Journal of Allergy and Clinical Immunology. 134: 46-55. PMID 24315451 DOI: 10.1016/J.Jaci.2013.08.053  1
2014 Kosova G, Hotaling JM, Ohlander S, Niederberger C, Prins GS, Ober C. Variants in DPF3 and DSCAML1 are associated with sperm morphology. Journal of Assisted Reproduction and Genetics. 31: 131-7. PMID 24271036 DOI: 10.1007/S10815-013-0140-9  1
2014 Yao TC, Du G, Han L, Sun Y, Hu D, Yang JJ, Mathias R, Roth LA, Rafaels N, Thompson EE, Loisel DA, Anderson R, Eng C, Arruabarrena Orbegozo M, Young M, ... ... Ober C, et al. Genome-wide association study of lung function phenotypes in a founder population. The Journal of Allergy and Clinical Immunology. 133: 248-55.e1-10. PMID 23932459 DOI: 10.1016/J.Jaci.2013.06.018  1
2013 Abe K, Ohno Y, Sassa T, Taguchi R, Çalışkan M, Ober C, Kihara A. Mutation for nonsyndromic mental retardation in the trans-2-enoyl-CoA reductase TER gene involved in fatty acid elongation impairs the enzyme activity and stability, leading to change in sphingolipid profile. The Journal of Biological Chemistry. 288: 36741-9. PMID 24220030 DOI: 10.1074/Jbc.M113.493221  1
2013 Gerull B, Kirchner F, Chong JX, Tagoe J, Chandrasekharan K, Strohm O, Waggoner D, Ober C, Duff HJ. Homozygous founder mutation in desmocollin-2 (DSC2) causes arrhythmogenic cardiomyopathy in the Hutterite population. Circulation. Cardiovascular Genetics. 6: 327-36. PMID 23863954 DOI: 10.1161/Circgenetics.113.000097  1
2013 Bögershausen N, Shahrzad N, Chong JX, von Kleist-Retzow JC, Stanga D, Li Y, Bernier FP, Loucks CM, Wirth R, Puffenberger EG, Hegele RA, Schreml J, Lapointe G, Keupp K, Brett CL, ... ... Ober C, et al. Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability. American Journal of Human Genetics. 93: 181-90. PMID 23830518 DOI: 10.1016/J.Ajhg.2013.05.028  1
2013 Beaulieu CL, Huang L, Innes AM, Akimenko MA, Puffenberger EG, Schwartz C, Jerry P, Ober C, Hegele RA, McLeod DR, Schwartzentruber J, Majewski J, Bulman DE, Parboosingh JS, et al. Intellectual disability associated with a homozygous missense mutation in THOC6. Orphanet Journal of Rare Diseases. 8: 62. PMID 23621916 DOI: 10.1186/1750-1172-8-62  1
2013 Lopes AM, Aston KI, Thompson E, Carvalho F, Gonçalves J, Huang N, Matthiesen R, Noordam MJ, Quintela I, Ramu A, Seabra C, Wilfert AB, Dai J, Downie JM, Fernandes S, ... ... Ober C, et al. Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1. Plos Genetics. 9: e1003349. PMID 23555275 DOI: 10.1371/Journal.Pgen.1003349  1
2013 Nicodemus-Johnson J, Laxman B, Stern RK, Sudi J, Tierney CN, Norwick L, Hogarth DK, McConville JF, Naureckas ET, Sperling AI, Solway J, Krishnan JA, Nicolae DL, White SR, Ober C. Maternal asthma and microRNA regulation of soluble HLA-G in the airway. The Journal of Allergy and Clinical Immunology. 131: 1496-503. PMID 23534973 DOI: 10.1016/J.Jaci.2013.01.037  1
2013 Calışkan M, Bochkov YA, Kreiner-Møller E, Bønnelykke K, Stein MM, Du G, Bisgaard H, Jackson DJ, Gern JE, Lemanske RF, Nicolae DL, Ober C. Rhinovirus wheezing illness and genetic risk of childhood-onset asthma. The New England Journal of Medicine. 368: 1398-407. PMID 23534543 DOI: 10.1056/Nejmoa1211592  1
2013 Melén E, Granell R, Kogevinas M, Strachan D, Gonzalez JR, Wjst M, Jarvis D, Ege M, Braun-Fahrländer C, Genuneit J, Horak E, Bouzigon E, Demenais F, Kauffmann F, Siroux V, ... ... Ober C, et al. Genome-wide association study of body mass index in 23 000 individuals with and without asthma. Clinical and Experimental Allergy : Journal of the British Society For Allergy and Clinical Immunology. 43: 463-74. PMID 23517042 DOI: 10.1111/Cea.12054  1
2013 Himes BE, Sheppard K, Berndt A, Leme AS, Myers RA, Gignoux CR, Levin AM, Gauderman WJ, Yang JJ, Mathias RA, Romieu I, Torgerson DG, Roth LA, Huntsman S, Eng C, ... ... Ober C, et al. Integration of mouse and human genome-wide association data identifies KCNIP4 as an asthma gene. Plos One. 8: e56179. PMID 23457522 DOI: 10.1371/Journal.Pone.0056179  1
2013 Thompson EE, Myers RA, Du G, Aydelotte TM, Tisler CJ, Stern DA, Evans MD, Graves PE, Jackson DJ, Martinez FD, Gern JE, Wright AL, Lemanske RF, Ober C. Maternal microchimerism protects against the development of asthma. The Journal of Allergy and Clinical Immunology. 132: 39-44. PMID 23434286 DOI: 10.1016/J.Jaci.2012.12.1575  1
2013 Levin AM, Mathias RA, Huang L, Roth LA, Daley D, Myers RA, Himes BE, Romieu I, Yang M, Eng C, Park JE, Zoratti K, Gignoux CR, Torgerson DG, Galanter JM, ... ... Ober C, et al. A meta-analysis of genome-wide association studies for serum total IgE in diverse study populations. The Journal of Allergy and Clinical Immunology. 131: 1176-84. PMID 23146381 DOI: 10.1016/J.Jaci.2012.10.002  1
2013 Loisel DA, Billstrand C, Murray K, Patterson K, Chaiworapongsa T, Romero R, Ober C. The maternal HLA-G 1597ΔC null mutation is associated with increased risk of pre-eclampsia and reduced HLA-G expression during pregnancy in African-American women. Molecular Human Reproduction. 19: 144-52. PMID 23002110 DOI: 10.1093/Molehr/Gas041  1
2012 Ségurel L, Thompson EE, Flutre T, Lovstad J, Venkat A, Margulis SW, Moyse J, Ross S, Gamble K, Sella G, Ober C, Przeworski M. The ABO blood group is a trans-species polymorphism in primates. Proceedings of the National Academy of Sciences of the United States of America. 109: 18493-8. PMID 23091028 DOI: 10.1073/Pnas.1210603109  1
2012 Myers RA, Himes BE, Gignoux CR, Yang JJ, Gauderman WJ, Rebordosa C, Xie J, Torgerson DG, Levin AM, Baurley J, Graves PE, Mathias RA, Romieu I, Roth LA, Conti D, ... ... Ober C, et al. Further replication studies of the EVE Consortium meta-analysis identifies 2 asthma risk loci in European Americans. The Journal of Allergy and Clinical Immunology. 130: 1294-301. PMID 23040885 DOI: 10.1016/J.Jaci.2012.07.054  1
2012 Campbell CD, Chong JX, Malig M, Ko A, Dumont BL, Han L, Vives L, O'Roak BJ, Sudmant PH, Shendure J, Abney M, Ober C, Eichler EE. Estimating the human mutation rate using autozygosity in a founder population. Nature Genetics. 44: 1277-81. PMID 23001126 DOI: 10.1038/Ng.2418  1
2012 Chong JX, Ouwenga R, Anderson RL, Waggoner DJ, Ober C. A population-based study of autosomal-recessive disease-causing mutations in a founder population. American Journal of Human Genetics. 91: 608-20. PMID 22981120 DOI: 10.1016/J.Ajhg.2012.08.007  1
2012 Ding D, Scott NM, Thompson EE, Chaiworapongsa T, Torres R, Billstrand C, Murray K, Dexheimer PJ, Ismail M, Kay H, Levy S, Romero R, Lindheimer MD, Nicolae DL, Ober C. Increased protein-coding mutations in the mitochondrial genome of African American women with preeclampsia. Reproductive Sciences (Thousand Oaks, Calif.). 19: 1343-51. PMID 22902742 DOI: 10.1177/1933719112450337  1
2012 Li X, Ampleford EJ, Howard TD, Moore WC, Torgerson DG, Li H, Busse WW, Castro M, Erzurum SC, Israel E, Nicolae DL, Ober C, Wenzel SE, Hawkins GA, Bleecker ER, et al. Genome-wide association studies of asthma indicate opposite immunopathogenesis direction from autoimmune diseases. The Journal of Allergy and Clinical Immunology. 130: 861-8.e7. PMID 22694930 DOI: 10.1097/01.Wox.0000411861.60664.A3  1
2012 Jassem RM, Shani WS, Loisel DA, Sharief M, Billstrand C, Ober C. HLA-G polymorphisms and soluble HLA-G protein levels in women with recurrent pregnancy loss from Basrah province in Iraq. Human Immunology. 73: 811-7. PMID 22651916 DOI: 10.1016/J.Humimm.2012.05.009  1
2012 Kosova G, Scott NM, Niederberger C, Prins GS, Ober C. Genome-wide association study identifies candidate genes for male fertility traits in humans. American Journal of Human Genetics. 90: 950-61. PMID 22633400 DOI: 10.1016/J.Ajhg.2012.04.016  1
2012 Torgerson DG, Capurso D, Ampleford EJ, Li X, Moore WC, Gignoux CR, Hu D, Eng C, Mathias RA, Busse WW, Castro M, Erzurum SC, Fitzpatrick AM, Gaston B, Israel E, ... ... Ober C, et al. Genome-wide ancestry association testing identifies a common European variant on 6q14.1 as a risk factor for asthma in African American subjects. The Journal of Allergy and Clinical Immunology. 130: 622-629.e9. PMID 22607992 DOI: 10.1016/J.Jaci.2012.03.045  1
2012 Thornton T, Zhang Q, Cai X, Ober C, McPeek MS. XM: association testing on the X-chromosome in case-control samples with related individuals. Genetic Epidemiology. 36: 438-50. PMID 22552845 DOI: 10.1002/Gepi.21638  1
2012 Welt CK, Styrkarsdottir U, Ehrmann DA, Thorleifsson G, Arason G, Gudmundsson JA, Ober C, Rosenfield RL, Saxena R, Thorsteinsdottir U, Crowley WF, Stefansson K. Variants in DENND1A are associated with polycystic ovary syndrome in women of European ancestry. The Journal of Clinical Endocrinology and Metabolism. 97: E1342-7. PMID 22547425 DOI: 10.1210/jc.2011-3478  1
2012 Loucks C, Parboosingh JS, Chong JX, Ober C, Siu VM, Hegele RA, Rupar CA, McLeod DR, Pinto A, Chudley AE, Innes AM. A shared founder mutation underlies restrictive dermopathy in Old Colony (Dutch-German) Mennonite and Hutterite patients in North America. American Journal of Medical Genetics. Part A. 158: 1229-32. PMID 22495976 DOI: 10.1002/Ajmg.A.35302  1
2012 Uricchio LH, Chong JX, Ross KD, Ober C, Nicolae DL. Accurate imputation of rare and common variants in a founder population from a small number of sequenced individuals. Genetic Epidemiology. 36: 312-9. PMID 22460724 DOI: 10.1002/Gepi.21623  1
2012 Meyer WK, Arbeithuber B, Ober C, Ebner T, Tiemann-Boege I, Hudson RR, Przeworski M. Evaluating the evidence for transmission distortion in human pedigrees. Genetics. 191: 215-32. PMID 22377632 DOI: 10.1534/Genetics.112.139576  1
2012 Perry GH, Xue Y, Smith RS, Meyer WK, Calışkan M, Yanez-Cuna O, Lee AS, Gutiérrez-Arcelus M, Ober C, Hollox EJ, Tyler-Smith C, Lee C. Evolutionary genetics of the human Rh blood group system. Human Genetics. 131: 1205-16. PMID 22367406 DOI: 10.1007/S00439-012-1147-5  1
2012 Torgerson DG, Capurso D, Mathias RA, Graves PE, Hernandez RD, Beaty TH, Bleecker ER, Raby BA, Meyers DA, Barnes KC, Weiss ST, Martinez FD, Nicolae DL, Ober C. Resequencing candidate genes implicates rare variants in asthma susceptibility. American Journal of Human Genetics. 90: 273-81. PMID 22325360 DOI: 10.1016/J.Ajhg.2012.01.008  1
2012 Cusanovich DA, Billstrand C, Zhou X, Chavarria C, De Leon S, Michelini K, Pai AA, Ober C, Gilad Y. The combination of a genome-wide association study of lymphocyte count and analysis of gene expression data reveals novel asthma candidate genes. Human Molecular Genetics. 21: 2111-23. PMID 22286170 DOI: 10.1093/Hmg/Dds021  1
2011 Huang L, Szymanska K, Jensen VL, Janecke AR, Innes AM, Davis EE, Frosk P, Li C, Willer JR, Chodirker BN, Greenberg CR, McLeod DR, Bernier FP, Chudley AE, Müller T, ... ... Ober C, et al. TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone. American Journal of Human Genetics. 89: 713-30. PMID 22152675 DOI: 10.1016/J.Ajhg.2011.11.005  1
2011 Kurina LM, Knutson KL, Hawkley LC, Cacioppo JT, Lauderdale DS, Ober C. Loneliness is associated with sleep fragmentation in a communal society. Sleep. 34: 1519-26. PMID 22043123 DOI: 10.5665/Sleep.1390  1
2011 Motika CA, Papachristou C, Abney M, Lester LA, Ober C. Rising prevalence of asthma is sex-specific in a US farming population. The Journal of Allergy and Clinical Immunology. 128: 774-9. PMID 21840584 DOI: 10.1016/j.jaci.2011.06.046  1
2011 Torgerson DG, Ampleford EJ, Chiu GY, Gauderman WJ, Gignoux CR, Graves PE, Himes BE, Levin AM, Mathias RA, Hancock DB, Baurley JW, Eng C, Stern DA, Celedón JC, Rafaels N, ... ... Ober C, et al. Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations. Nature Genetics. 43: 887-92. PMID 21804549 DOI: 10.1038/Ng.888  1
2011 Loisel DA, Tan Z, Tisler CJ, Evans MD, Gangnon RE, Jackson DJ, Gern JE, Lemanske RF, Ober C. IFNG genotype and sex interact to influence the risk of childhood asthma. The Journal of Allergy and Clinical Immunology. 128: 524-31. PMID 21798578 DOI: 10.1016/J.Jaci.2011.06.016  1
2011 Ober C, Yao TC. The genetics of asthma and allergic disease: a 21st century perspective. Immunological Reviews. 242: 10-30. PMID 21682736 DOI: 10.1111/j.1600-065X.2011.01029.x  1
2011 Topper S, Ober C, Das S. Exome sequencing and the genetics of intellectual disability. Clinical Genetics. 80: 117-26. PMID 21627642 DOI: 10.1111/j.1399-0004.2011.01720.x  1
2011 Chong JX, Oktay AA, Dai Z, Swoboda KJ, Prior TW, Ober C. A common spinal muscular atrophy deletion mutation is present on a single founder haplotype in the US Hutterites. European Journal of Human Genetics : Ejhg. 19: 1045-51. PMID 21610747 DOI: 10.1038/Ejhg.2011.85  1
2011 Papachristou C, Ober C, Abney M. Genetic variance components estimation for binary traits using multiple related individuals. Genetic Epidemiology. 35: 291-302. PMID 21465547 DOI: 10.1002/gepi.20577  1
2011 Caliskan M, Cusanovich DA, Ober C, Gilad Y. The effects of EBV transformation on gene expression levels and methylation profiles. Human Molecular Genetics. 20: 1643-52. PMID 21289059 DOI: 10.1093/Hmg/Ddr041  1
2011 Ober C, Vercelli D. Gene-environment interactions in human disease: nuisance or opportunity? Trends in Genetics : Tig. 27: 107-15. PMID 21216485 DOI: 10.1016/J.Tig.2010.12.004  1
2011 Çalışkan M, Chong JX, Uricchio L, Anderson R, Chen P, Sougnez C, Garimella K, Gabriel SB, dePristo MA, Shakir K, Matern D, Das S, Waggoner D, Nicolae DL, Ober C. Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13. Human Molecular Genetics. 20: 1285-9. PMID 21212097 DOI: 10.1093/Hmg/Ddq569  1
2011 Alvarado Arnez LE, Venegas EN, Ober C, Thompson EE. Sequence variation in the IL4 gene and resistance to Trypanosoma cruzi infection in Bolivians. The Journal of Allergy and Clinical Immunology. 127: 279-82, 282.e1-3. PMID 21211660 DOI: 10.1016/J.Jaci.2010.10.026  1
2011 Gamble KC, Moyse JA, Lovstad JN, Ober CB, Thompson EE. Blood groups in the Species Survival Plan®, European endangered species program, and managed in situ populations of bonobo (Pan paniscus), common chimpanzee (Pan troglodytes), gorilla (Gorilla ssp.), and orangutan (Pongo pygmaeus ssp.). Zoo Biology. 30: 427-44. PMID 20853409 DOI: 10.1002/Zoo.20348  1
2010 Ober C, Butte AJ, Elias JA, Lusis AJ, Gan W, Banks-Schlegel S, Schwartz D. Getting from genes to function in lung disease: a National Heart, Lung, and Blood Institute workshop report. American Journal of Respiratory and Critical Care Medicine. 182: 732-7. PMID 20558629 DOI: 10.1164/Rccm.201002-0180Pp  1
2010 Kosova G, Pickrell JK, Kelley JL, McArdle PF, Shuldiner AR, Abney M, Ober C. The CFTR Met 470 allele is associated with lower birth rates in fertile men from a population isolate. Plos Genetics. 6: e1000974. PMID 20532200 DOI: 10.1371/Journal.Pgen.1000974  1
2010 White SR, Loisel DA, McConville JF, Stern R, Tu Y, Marroquin BA, Noth I, Ober C. Levels of soluble human leukocyte antigen-G are increased in asthmatic airways. The European Respiratory Journal. 35: 925-7. PMID 20356990 DOI: 10.1183/09031936.00164809  1
2010 Baudat F, Buard J, Grey C, Fledel-Alon A, Ober C, Przeworski M, Coop G, de Massy B. PRDM9 is a major determinant of meiotic recombination hotspots in humans and mice. Science (New York, N.Y.). 327: 836-40. PMID 20044539 DOI: 10.1126/Science.1183439  1
2010 Thompson EE, Haller G, Pinto JM, Sun Y, Zelano B, Jacob S, McClintock MK, Nicolae DL, Ober C. Sequence variations at the human leukocyte antigen-linked olfactory receptor cluster do not influence female preferences for male odors. Human Immunology. 71: 100-3. PMID 19833159 DOI: 10.1016/J.Humimm.2009.10.004  1
2010 Kosova G, Abney M, Ober C. Colloquium papers: Heritability of reproductive fitness traits in a human population. Proceedings of the National Academy of Sciences of the United States of America. 107: 1772-8. PMID 19822755 DOI: 10.1073/Pnas.0906196106  1
2010 Thompson EE, Sun Y, Nicolae D, Ober C. Shades of gray: a comparison of linkage disequilibrium between Hutterites and Europeans. Genetic Epidemiology. 34: 133-9. PMID 19697328 DOI: 10.1002/Gepi.20442  1
2010 Loisel DA, Alberts SC, Ober C. Functional significance of MHC variation in mate choice, reproductive outcome, and disease risk Evolution in Health and Disease. DOI: 10.1093/acprof:oso/9780199207466.003.0008  1
2009 Haller G, Torgerson DG, Ober C, Thompson EE. Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility. The Journal of Allergy and Clinical Immunology. 124: 1204-9.e9. PMID 19910025 DOI: 10.1016/J.Jaci.2009.09.013  1
2009 Fledel-Alon A, Wilson DJ, Broman K, Wen X, Ober C, Coop G, Przeworski M. Broad-scale recombination patterns underlying proper disjunction in humans. Plos Genetics. 5: e1000658. PMID 19763175 DOI: 10.1371/Journal.Pgen.1000658  1
2009 Ober C, Chupp GL. The chitinase and chitinase-like proteins: a review of genetic and functional studies in asthma and immune-mediated diseases. Current Opinion in Allergy and Clinical Immunology. 9: 401-8. PMID 19644363 DOI: 10.1097/ACI.0b013e3283306533  1
2009 Nicolae DL, Ober C. (Too) great expectations: the challenges in replicating asthma disease genes. American Journal of Respiratory and Critical Care Medicine. 179: 1078-9. PMID 19498061 DOI: 10.1164/rccm.200903-0456ED  1
2009 Bellenguez C, Ober C, Bourgain C. Linkage analysis with dense SNP maps in isolated populations. Human Heredity. 68: 87-97. PMID 19365135 DOI: 10.1159/000212501  1
2009 Ober C, Nord AS, Thompson EE, Pan L, Tan Z, Cusanovich D, Sun Y, Nicolae R, Edelstein C, Schneider DH, Billstrand C, Pfaffinger D, Phillips N, Anderson RL, Philips B, et al. Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6q. Journal of Lipid Research. 50: 798-806. PMID 19124843 DOI: 10.1194/Jlr.M800515-Jlr200  1
2009 Wang Y, O'Connell JR, McArdle PF, Wade JB, Dorff SE, Shah SJ, Shi X, Pan L, Rampersaud E, Shen H, Kim JD, Subramanya AR, Steinle NI, Parsa A, Ober CC, et al. From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene. Proceedings of the National Academy of Sciences of the United States of America. 106: 226-31. PMID 19114657 DOI: 10.1073/Pnas.0808358106  1
2009 Bellenguez C, Ober C, Bourgain C. A multiple splitting approach to linkage analysis in large pedigrees identifies a linkage to asthma on chromosome 12. Genetic Epidemiology. 33: 207-16. PMID 18839415 DOI: 10.1002/gepi.20371  1
2008 Ober C, Loisel DA, Gilad Y. Sex-specific genetic architecture of human disease. Nature Reviews. Genetics. 9: 911-22. PMID 19002143 DOI: 10.1038/Nrg2415  1
2008 Pinto JM, Hayes MG, Schneider D, Naclerio RM, Ober C. A genomewide screen for chronic rhinosinusitis genes identifies a locus on chromosome 7q. The Laryngoscope. 118: 2067-72. PMID 18622306 DOI: 10.1097/MLG.0b013e3181805147  1
2008 Ma SF, Flores C, Wade MS, Dudek SM, Nicolae DL, Ober C, Garcia JG. A common cortactin gene variation confers differential susceptibility to severe asthma. Genetic Epidemiology. 32: 757-66. PMID 18521921 DOI: 10.1002/gepi.20343  1
2008 Nolan DK, Chen P, Das S, Ober C, Waggoner D. Fine mapping of a locus for nonsyndromic mental retardation on chromosome 19p13. American Journal of Medical Genetics. Part A. 146: 1414-22. PMID 18446860 DOI: 10.1002/ajmg.a.32307  1
2008 Ober C, Tan Z, Sun Y, Possick JD, Pan L, Nicolae R, Radford S, Parry RR, Heinzmann A, Deichmann KA, Lester LA, Gern JE, Lemanske RF, Nicolae DL, Elias JA, et al. Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function. The New England Journal of Medicine. 358: 1682-91. PMID 18403759 DOI: 10.1056/Nejmoa0708801  1
2008 Gudmundsson J, Sulem P, Rafnar T, Bergthorsson JT, Manolescu A, Gudbjartsson D, Agnarsson BA, Sigurdsson A, Benediktsdottir KR, Blondal T, Jakobsdottir M, Stacey SN, Kostic J, Kristinsson KT, Birgisdottir B, ... ... Ober C, et al. Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer. Nature Genetics. 40: 281-3. PMID 18264098 DOI: 10.1038/Ng.89  1
2008 Pinto JM, Thanaviratananich S, Hayes MG, Naclerio RM, Ober C. A genome-wide screen for hyposmia susceptibility Loci. Chemical Senses. 33: 319-29. PMID 18245794 DOI: 10.1093/chemse/bjm092  1
2008 Coop G, Wen X, Ober C, Pritchard JK, Przeworski M. High-resolution mapping of crossovers reveals extensive variation in fine-scale recombination patterns among humans. Science (New York, N.Y.). 319: 1395-8. PMID 18239090 DOI: 10.1126/Science.1151851  1
2008 Neidich AB, Joseph JW, Ober C, Ross LF. Empirical data about women's attitudes towards a hypothetical pediatric biobank. American Journal of Medical Genetics. Part A. 146: 297-304. PMID 18205141 DOI: 10.1002/ajmg.a.32145  1
2008 Joseph JW, Neidich AB, Ober C, Ross LF. Empirical data about women's attitudes toward a biobank focused on pregnancy outcomes. American Journal of Medical Genetics. Part A. 146: 305-11. PMID 18203186 DOI: 10.1002/ajmg.a.32146  1
2008 Gallego Romero I, Ober C. CFTR mutations and reproductive outcomes in a population isolate. Human Genetics. 122: 583-8. PMID 17901983 DOI: 10.1007/s00439-007-0432-1  1
2007 Gudmundsson J, Sulem P, Steinthorsdottir V, Bergthorsson JT, Thorleifsson G, Manolescu A, Rafnar T, Gudbjartsson D, Agnarsson BA, Baker A, Sigurdsson A, Benediktsdottir KR, Jakobsdottir M, Blondal T, Stacey SN, ... ... Ober C, et al. Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes. Nature Genetics. 39: 977-83. PMID 17603485 DOI: 10.1038/Ng2062  1
2007 Pluzhnikov A, Nolan DK, Tan Z, McPeek MS, Ober C. Correlation of intergenerational family sizes suggests a genetic component of reproductive fitness. American Journal of Human Genetics. 81: 165-9. PMID 17564973 DOI: 10.1086/518446  1
2007 Thompson EE, Pan L, Ostrovnaya I, Weiss LA, Gern JE, Lemanske RF, Nicolae DL, Ober C. Integrin beta 3 genotype influences asthma and allergy phenotypes in the first 6 years of life. The Journal of Allergy and Clinical Immunology. 119: 1423-9. PMID 17556058 DOI: 10.1016/J.Jaci.2007.03.029  1
2007 Gudmundsson J, Sulem P, Manolescu A, Amundadottir LT, Gudbjartsson D, Helgason A, Rafnar T, Bergthorsson JT, Agnarsson BA, Baker A, Sigurdsson A, Benediktsdottir KR, Jakobsdottir M, Xu J, Blondal T, ... ... Ober C, et al. Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24. Nature Genetics. 39: 631-7. PMID 17401366 DOI: 10.1038/Ng1999  1
2007 Pan L, Ober C, Abney M. Heritability estimation of sex-specific effects on human quantitative traits. Genetic Epidemiology. 31: 338-47. PMID 17323368 DOI: 10.1002/gepi.20214  1
2006 Kurz T, Hoffjan S, Hayes MG, Schneider D, Nicolae R, Heinzmann A, Jerkic SP, Parry R, Cox NJ, Deichmann KA, Ober C. Fine mapping and positional candidate studies on chromosome 5p13 identify multiple asthma susceptibility loci. The Journal of Allergy and Clinical Immunology. 118: 396-402. PMID 16890764 DOI: 10.1016/j.jaci.2006.04.036  1
2006 Weiss LA, Kosova G, Delahanty RJ, Jiang L, Cook EH, Ober C, Sutcliffe JS. Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility. European Journal of Human Genetics : Ejhg. 14: 923-31. PMID 16724005 DOI: 10.1038/Sj.Ejhg.5201644  1
2006 Weiss LA, Ober C, Cook EH. ITGB3 shows genetic and expression interaction with SLC6A4. Human Genetics. 120: 93-100. PMID 16721604 DOI: 10.1007/s00439-006-0196-z  1
2006 Amundadottir LT, Sulem P, Gudmundsson J, Helgason A, Baker A, Agnarsson BA, Sigurdsson A, Benediktsdottir KR, Cazier JB, Sainz J, Jakobsdottir M, Kostic J, Magnusdottir DN, Ghosh S, Agnarsson K, ... ... Ober C, et al. A common variant associated with prostate cancer in European and African populations. Nature Genetics. 38: 652-8. PMID 16682969 DOI: 10.1038/Ng1808  1
2006 Ober C, Billstrand C, Kuldanek S, Tan Z. The miscarriage-associated HLA-G -725G allele influences transcription rates in JEG-3 cells. Human Reproduction (Oxford, England). 21: 1743-8. PMID 16501035 DOI: 10.1093/humrep/del036  1
2006 Chan A, Newman DL, Shon AM, Schneider DH, Kuldanek S, Ober C. Variation in the type I interferon gene cluster on 9p21 influences susceptibility to asthma and atopy. Genes and Immunity. 7: 169-78. PMID 16437122 DOI: 10.1038/Sj.Gene.6364287  1
2006 Weiss LA, Pan L, Abney M, Ober C. The sex-specific genetic architecture of quantitative traits in humans. Nature Genetics. 38: 218-22. PMID 16429159 DOI: 10.1038/ng1726  1
2006 Ober C, Hoffjan S. Asthma genetics 2006: the long and winding road to gene discovery. Genes and Immunity. 7: 95-100. PMID 16395390 DOI: 10.1038/sj.gene.6364284  1
2005 Ober C. HLA-G: an asthma gene on chromosome 6p. Immunology and Allergy Clinics of North America. 25: 669-79. PMID 16257632 DOI: 10.1016/j.iac.2005.08.001  1
2005 Tan Z, Shon AM, Ober C. Evidence of balancing selection at the HLA-G promoter region. Human Molecular Genetics. 14: 3619-28. PMID 16236759 DOI: 10.1093/hmg/ddi389  1
2005 Ober C, Thompson EE. Rethinking genetic models of asthma: the role of environmental modifiers. Current Opinion in Immunology. 17: 670-8. PMID 16214315 DOI: 10.1016/J.Coi.2005.09.009  1
2005 Ober C. Perspectives on the past decade of asthma genetics. The Journal of Allergy and Clinical Immunology. 116: 274-8. PMID 16083779 DOI: 10.1016/j.jaci.2005.04.039  1
2005 Shilling RA, Pinto JM, Decker DC, Schneider DH, Bandukwala HS, Schneider JR, Camoretti-Mercado B, Ober C, Sperling AI. Cutting edge: polymorphisms in the ICOS promoter region are associated with allergic sensitization and Th2 cytokine production. Journal of Immunology (Baltimore, Md. : 1950). 175: 2061-5. PMID 16081771 DOI: 10.4049/Jimmunol.175.4.2061  0.44
2005 Zhang J, Schneider D, Ober C, McPeek MS. Multilocus linkage disequilibrium mapping by the decay of haplotype sharing with samples of related individuals. Genetic Epidemiology. 29: 128-40. PMID 16049966 DOI: 10.1002/Gepi.20081  1
2005 Kurina LM, Weiss LA, Graves SW, Parry R, Williams GH, Abney M, Ober C. Sex differences in the genetic basis of morning serum cortisol levels: genome-wide screen identifies two novel loci specific to women. The Journal of Clinical Endocrinology and Metabolism. 90: 4747-52. PMID 15941864 DOI: 10.1210/Jc.2005-0384  1
2005 Hunt JS, Petroff MG, McIntire RH, Ober C. HLA-G and immune tolerance in pregnancy. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 19: 681-93. PMID 15857883 DOI: 10.1096/Fj.04-2078Rev  1
2005 Weiss LA, Abney M, Parry R, Scanu AM, Cook EH, Ober C. Variation in ITGB3 has sex-specific associations with plasma lipoprotein(a) and whole blood serotonin levels in a population-based sample. Human Genetics. 117: 81-7. PMID 15834589 DOI: 10.1007/s00439-004-1250-3  1
2005 Weiss LA, Lester LA, Gern JE, Wolf RL, Parry R, Lemanske RF, Solway J, Ober C. Variation in ITGB3 is associated with asthma and sensitization to mold allergen in four populations. American Journal of Respiratory and Critical Care Medicine. 172: 67-73. PMID 15817799 DOI: 10.1164/rccm.200411-1555OC  1
2005 McClintock MK, Bullivant S, Jacob S, Spencer N, Zelano B, Ober C. Human body scents: conscious perceptions and biological effects. Chemical Senses. 30: i135-7. PMID 15738077 DOI: 10.1093/Chemse/Bjh151  1
2005 Hoffjan S, Nicolae D, Ostrovnaya I, Roberg K, Evans M, Mirel DB, Steiner L, Walker K, Shult P, Gangnon RE, Gern JE, Martinez FD, Lemanske RF, Ober C. Gene-environment interaction effects on the development of immune responses in the 1st year of life. American Journal of Human Genetics. 76: 696-704. PMID 15726497 DOI: 10.1086/429418  1
2005 Weiss LA, Abney M, Cook EH, Ober C. Sex-specific genetic architecture of whole blood serotonin levels. American Journal of Human Genetics. 76: 33-41. PMID 15526234 DOI: 10.1086/426697  1
2005 Kurina LM, Weiss LA, Graves SW, Parry R, Williams GH, Abney M, Ober C. 431: Genome-Wide Screen Identifies Two Novel Loci Associated with Morning Serum Cortisol Levels in Women American Journal of Epidemiology. 161. DOI: 10.1093/Aje/161.Supplement_1.S108B  0.52
2004 Bourgain C, Abney M, Schneider D, Ober C, McPeek MS. Testing for Hardy-Weinberg equilibrium in samples with related individuals. Genetics. 168: 2349-61. PMID 15371359 DOI: 10.1534/Genetics.104.031617  1
2004 Kurz T, Ober C. The role of environmental tobacco smoke in genetic susceptibility to asthma. Current Opinion in Allergy and Clinical Immunology. 4: 335-9. PMID 15349030 DOI: 10.1097/00130832-200410000-00002  1
2004 Dobyns WB, Filauro A, Tomson BN, Chan AS, Ho AW, Ting NT, Oosterwijk JC, Ober C. Inheritance of most X-linked traits is not dominant or recessive, just X-linked. American Journal of Medical Genetics. Part A. 129: 136-43. PMID 15316978 DOI: 10.1002/Ajmg.A.30123  1
2004 Weiss LA, Veenstra-Vanderweele J, Newman DL, Kim SJ, Dytch H, McPeek MS, Cheng S, Ober C, Cook EH, Abney M. Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin. European Journal of Human Genetics : Ejhg. 12: 949-54. PMID 15292919 DOI: 10.1038/Sj.Ejhg.5201239  1
2004 McPeek MS, Wu X, Ober C. Best linear unbiased allele-frequency estimation in complex pedigrees. Biometrics. 60: 359-67. PMID 15180661 DOI: 10.1111/J.0006-341X.2004.00180.X  1
2004 Newman DL, Hoffjan S, Bourgain C, Abney M, Nicolae RI, Profits ET, Grow MA, Walker K, Steiner L, Parry R, Reynolds R, McPeek MS, Cheng S, Ober C. Are common disease susceptibility alleles the same in outbred and founder populations? European Journal of Human Genetics : Ejhg. 12: 584-90. PMID 15100713 DOI: 10.1038/Sj.Ejhg.5201191  1
2004 Blumenthal MN, Ober C, Beaty TH, Bleecker ER, Langefeld CD, King RA, Lester L, Cox N, Barnes K, Togias A, Mathias R, Meyers DA, Oetting W, Rich SS. Genome scan for loci linked to mite sensitivity: the Collaborative Study on the Genetics of Asthma (CSGA). Genes and Immunity. 5: 226-31. PMID 15029235 DOI: 10.1038/Sj.Gene.6364063  1
2004 Gern JE, Reardon CL, Hoffjan S, Nicolae D, Li Z, Roberg KA, Neaville WA, Carlson-Dakes K, Adler K, Hamilton R, Anderson E, Gilbertson-White S, Tisler C, Dasilva D, Anklam K, ... ... Ober C, et al. Effects of dog ownership and genotype on immune development and atopy in infancy. The Journal of Allergy and Clinical Immunology. 113: 307-14. PMID 14767447 DOI: 10.1016/J.Jaci.2003.11.017  1
2004 Zöllner S, Wen X, Hanchard NA, Herbert MA, Ober C, Pritchard JK. Evidence for extensive transmission distortion in the human genome. American Journal of Human Genetics. 74: 62-72. PMID 14681832 DOI: 10.1086/381131  1
2004 Blumenthal MN, Langefeld CD, Beaty TH, Bleecker ER, Ober C, Lester L, Lange E, Barnes KC, Wolf R, King RA, Solway J, Oetting W, Meyers DA, Rich SS. A genome-wide search for allergic response (atopy) genes in three ethnic groups: Collaborative Study on the Genetics of Asthma. Human Genetics. 114: 157-64. PMID 14586638 DOI: 10.1007/S00439-003-1030-5  1
2003 Hoffjan S, Nicolae D, Ober C. Association studies for asthma and atopic diseases: a comprehensive review of the literature. Respiratory Research. 4: 14. PMID 14748924 DOI: 10.1186/1465-9921-4-14  1
2003 Hunt JS, Pace JL, Morales PJ, Ober C. Immunogenicity of the soluble isoforms of HLA-G. Molecular Human Reproduction. 9: 729-35. PMID 14561816 DOI: 10.1093/molehr/gag087  1
2003 Bourgain C, Hoffjan S, Nicolae R, Newman D, Steiner L, Walker K, Reynolds R, Ober C, McPeek MS. Novel case-control test in a founder population identifies P-selectin as an atopy-susceptibility locus. American Journal of Human Genetics. 73: 612-26. PMID 12929084 DOI: 10.1086/378208  1
2003 Sullivan AE, Lewis T, Stephenson M, Odem R, Schreiber J, Ober C, Branch DW. Pregnancy outcome in recurrent miscarriage patients with skewed X chromosome inactivation. Obstetrics and Gynecology. 101: 1236-42. PMID 12798530 DOI: 10.1016/S0029-7844(03)00345-4  1
2003 Ober C, Aldrich CL, Chervoneva I, Billstrand C, Rahimov F, Gray HL, Hyslop T. Variation in the HLA-G promoter region influences miscarriage rates. American Journal of Human Genetics. 72: 1425-35. PMID 12721954 DOI: 10.1086/375501  1
2003 Newman DL, Abney M, Dytch H, Parry R, McPeek MS, Ober C. Major loci influencing serum triglyceride levels on 2q14 and 9p21 localized by homozygosity-by-descent mapping in a large Hutterite pedigree. Human Molecular Genetics. 12: 137-44. PMID 12499394 DOI: 10.1093/Hmg/Ddg012  1
2002 Hoffjan S, Ober C. Present status on the genetic studies of asthma. Current Opinion in Immunology. 14: 709-17. PMID 12413520 DOI: 10.1016/S0952-7915(02)00393-X  1
2002 Bourgain C, Genin E, Ober C, Clerget-Darpoux F. Missing data in haplotype analysis: a study on the MILC method. Annals of Human Genetics. 66: 99-108. PMID 12022148 DOI: 10.1017/S000348000100896X  1
2002 Aldrich C, Wambebe C, Odama L, Di Rienzo A, Ober C. Linkage disequilibrium and age estimates of a deletion polymorphism (1597DeltaC) in HLA-G suggest non-neutral evolution. Human Immunology. 63: 405-12. PMID 11975984 DOI: 10.1016/S0198-8859(02)00377-4  1
2002 Abney M, Ober C, McPeek MS. Quantitative-trait homozygosity and association mapping and empirical genomewide significance in large, complex pedigrees: fasting serum-insulin level in the Hutterites. American Journal of Human Genetics. 70: 920-34. PMID 11880950 DOI: 10.1086/339705  1
2002 Jacob S, McClintock MK, Zelano B, Ober C. Paternally inherited HLA alleles are associated with women's choice of male odor. Nature Genetics. 30: 175-9. PMID 11799397 DOI: 10.1038/Ng830  1
2001 Ober C. Susceptibility genes in asthma and allergy. Current Allergy and Asthma Reports. 1: 174-9. PMID 11899300 DOI: 10.1007/S11882-001-0085-4  1
2001 Meyers DA, Wjst M, Ober C. Description of three data sets: Collaborative Study on the Genetics of Asthma (CSGA), the German Affected-Sib-Pair Study, and the Hutterites of South Dakota. Genetic Epidemiology. 21: S4-8. PMID 11793707 DOI: 10.1002/gepi.2001.21.s1.s4  1
2001 Gray HL, Sorensen EL, Hunt JS, Ober C. Three polymorphisms in the 3' UTR of the TRAIL (TNF-related apoptosis-inducing ligand) gene. Genes and Immunity. 2: 469-70. PMID 11781716 DOI: 10.1038/sj.gene.6363806  1
2001 Aldrich CL, Stephenson MD, Karrison T, Odem RR, Branch DW, Scott JR, Schreiber JR, Ober C. HLA-G genotypes and pregnancy outcome in couples with unexplained recurrent miscarriage. Molecular Human Reproduction. 7: 1167-72. PMID 11719594 DOI: 10.1093/Molehr/7.12.1167  1
2001 Newman DL, Abney M, McPeek MS, Ober C, Cox NJ. The importance of genealogy in determining genetic associations with complex traits. American Journal of Human Genetics. 69: 1146-8. PMID 11590549 DOI: 10.1086/323659  1
2001 Ober C, Abney M, McPeek MS. The genetic dissection of complex traits in a founder population. American Journal of Human Genetics. 69: 1068-79. PMID 11590547 DOI: 10.1086/324025  1
2001 Lester LA, Rich SS, Blumenthal MN, Togias A, Murphy S, Malveaux F, Miller ME, Dunston GM, Solway J, Wolf RL, Samet JM, Marsh DG, Meyers DA, Ober C, Bleecker ER, et al. Ethnic differences in asthma and associated phenotypes: collaborative study on the genetics of asthma. The Journal of Allergy and Clinical Immunology. 108: 357-62. PMID 11544453 DOI: 10.1067/Mai.2001.117796  1
2001 Wu X, Di Rienzo A, Ober C. A population genetics study of single nucleotide polymorphisms in the interleukin 4 receptor alpha (IL4RA) gene. Genes and Immunity. 2: 128-34. PMID 11426321 DOI: 10.1038/sj.gene.6363746  1
2001 Xu J, Meyers DA, Ober C, Blumenthal MN, Mellen B, Barnes KC, King RA, Lester LA, Howard TD, Solway J, Langefeld CD, Beaty TH, Rich SS, Bleecker ER, Cox NJ, et al. Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three U.S. populations: collaborative study on the genetics of asthma. American Journal of Human Genetics. 68: 1437-46. PMID 11349227 DOI: 10.1086/320589  1
2001 Abney M, McPeek MS, Ober C. Broad and narrow heritabilities of quantitative traits in a founder population. American Journal of Human Genetics. 68: 1302-7. PMID 11309690 DOI: 10.1086/320112  1
2001 Mathias RA, Freidhoff LR, Blumenthal MN, Meyers DA, Lester L, King R, Xu JF, Solway J, Barnes KC, Pierce J, Stine OC, Togias A, Oetting W, Marshik PL, Hetmanski JB, ... ... Ober C, et al. Genome-wide linkage analyses of total serum IgE using variance components analysis in asthmatic families. Genetic Epidemiology. 20: 340-55. PMID 11255243 DOI: 10.1002/Gepi.5  1
2000 Eklund AC, Ober C. Polymorphic microsatellite markers within the MHC of Peromyscus polionotus. Hereditas. 133: 179-81. PMID 11338432 DOI: 10.1111/J.1601-5223.2000.00179.X  1
2000 Hunt JS, Petroff MG, Morales P, Sedlmayr P, Geraghty DE, Ober C. HLA-G in reproduction: studies on the maternal-fetal interface. Human Immunology. 61: 1113-7. PMID 11137215 DOI: 10.1016/S0198-8859(00)00195-6  1
2000 Ober C, Tsalenko A, Parry R, Cox NJ. A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. American Journal of Human Genetics. 67: 1154-62. PMID 11022011 DOI: 10.1016/S0002-9297(07)62946-2  1
2000 Smith KL, Alberts SC, Bayes MK, Bruford MW, Altmann J, Ober C. Cross-species amplification, non-invasive genotyping, and non-Mendelian inheritance of human STRPs in Savannah baboons. American Journal of Primatology. 51: 219-27. PMID 10941438 DOI: 10.1002/1098-2345(200008)51:4<219::Aid-Ajp1>3.0.Co;2-G  1
2000 Summerhill E, Leavitt SA, Gidley H, Parry R, Solway J, Ober C. beta(2)-adrenergic receptor Arg16/Arg16 genotype is associated with reduced lung function, but not with asthma, in the Hutterites. American Journal of Respiratory and Critical Care Medicine. 162: 599-602. PMID 10934093 DOI: 10.1164/ajrccm.162.2.9910108  1
2000 Ober C, Moffatt MF. Contributing factors to the pathobiology. The genetics of asthma. Clinics in Chest Medicine. 21: 245-61. PMID 10907586 DOI: 10.1016/S0272-5231(05)70264-1  1
2000 Aldrich C, Verp MS, Walker MA, Ober C. A null mutation in HLA-G is not associated with preeclampsia or intrauterine growth retardation. Journal of Reproductive Immunology. 47: 41-8. PMID 10779589 DOI: 10.1016/S0165-0378(00)00052-8  1
2000 Génin E, Ober C, Weitkamp L, Thomson G. A robust test for assortative mating. European Journal of Human Genetics : Ejhg. 8: 119-24. PMID 10757643 DOI: 10.1038/Sj.Ejhg.5200430  1
2000 Abney M, McPeek MS, Ober C. Estimation of variance components of quantitative traits in inbred populations. American Journal of Human Genetics. 66: 629-50. PMID 10677322 DOI: 10.1086/302759  1
2000 Ober C, Leavitt SA, Tsalenko A, Howard TD, Hoki DM, Daniel R, Newman DL, Wu X, Parry R, Lester LA, Solway J, Blumenthal M, King RA, Xu J, Meyers DA, et al. Variation in the interleukin 4-receptor alpha gene confers susceptibility to asthma and atopy in ethnically diverse populations. American Journal of Human Genetics. 66: 517-26. PMID 10677312 DOI: 10.1086/302781  1
1999 Robertson A, Charlesworth D, Ober C. Effect of inbreeding avoidance on Hardy-Weinberg expectations: examples of neutral and selected loci. Genetic Epidemiology. 17: 165-73. PMID 10446464 DOI: 10.1002/(Sici)1098-2272(1999)17:3<165::Aid-Gepi2>3.0.Co;2-L  1
1999 Nickel RG, Willadsen SA, Freidhoff LR, Huang SK, Caraballo L, Naidu RP, Levett P, Blumenthal M, Banks-Schlegel S, Bleecker E, Beaty T, Ober C, Barnes KC. Determination of Duffy genotypes in three populations of African descent using PCR and sequence-specific oligonucleotides. Human Immunology. 60: 738-42. PMID 10439320 DOI: 10.1016/S0198-8859(99)00039-7  1
1999 Ober C, Karrison T, Odem RR, Barnes RB, Branch DW, Stephenson MD, Baron B, Walker MA, Scott JR, Schreiber JR. Mononuclear-cell immunisation in prevention of recurrent miscarriages: a randomised trial. Lancet. 354: 365-9. PMID 10437864 DOI: 10.1016/S0140-6736(98)12055-X  1
1999 Weitkamp LR, Ober C. Ancestral and recombinant 16-locus HLA haplotypes in the Hutterites. Immunogenetics. 49: 491-7. PMID 10380692 DOI: 10.1007/s002510050525  1
1999 Ober C. Studies of HLA, fertility and mate choice in a human isolate. Human Reproduction Update. 5: 103-7. PMID 10336015 DOI: 10.1093/humupd/5.2.103  1
1999 Kaufman KA, Bowen JA, Tsai AF, Bluestone JA, Hunt JS, Ober C. The CTLA-4 gene is expressed in placental fibroblasts. Molecular Human Reproduction. 5: 84-7. PMID 10050667 DOI: 10.1093/molehr/5.1.84  1
1999 Ober C, Hyslop T, Hauck WW. Inbreeding effects on fertility in humans: evidence for reproductive compensation. American Journal of Human Genetics. 64: 225-31. PMID 9915962 DOI: 10.1086/302198  1
1998 Tsai AF, Kaufman KA, Walker MA, Karrison TG, Odem RR, Barnes RB, Scott JR, Schreiber JR, Stephenson MD, Ober C. Transmission disequilibrium of maternally-inherited CTLA-4 microsatellite alleles in idiopathic recurrent miscarriage. Journal of Reproductive Immunology. 40: 147-57. PMID 9881742 DOI: 10.1016/S0165-0378(98)00073-4  1
1998 Grimsley C, Mather KA, Ober C. HLA-H: a pseudogene with increased variation due to balancing selection at neighboring loci. Molecular Biology and Evolution. 15: 1581-8. PMID 9866194 DOI: 10.1093/OXFORDJOURNALS.MOLBEV.A025886  1
1998 Van Der Ven K, Skrablin S, Ober C, Krebs D. HLA-G polymorphisms: Ethnic differences and implications for potential molecule function American Journal of Reproductive Immunology. 40: 145-157. PMID 9764358 DOI: 10.1111/j.1600-0897.1998.tb00406.x  1
1998 Karrison TG, Ober C. Recurrent miscarriage (REMIS) Study: How should data from women who do not become pregnant be handled? Controlled Clinical Trials. 19: 430-439. PMID 9741864 DOI: 10.1016/S0197-2456(98)00019-1  1
1998 Ober C, Cox NJ, Abney M, Di Rienzo A, Lander ES, Changyaleket B, Gidley H, Kurtz B, Lee J, Nance M, Pettersson A, Prescott J, Richardson A, Schlenker E, Summerhill E, et al. Genome-wide search for asthma susceptibility loci in a founder population. The Collaborative Study on the Genetics of Asthma. Human Molecular Genetics. 7: 1393-8. PMID 9700192 DOI: 10.1093/Hmg/7.9.1393  1
1998 Ober C, Aldrich C, Rosinsky B, Robertson A, Walker MA, Willadsen S, Verp MS, Geraghty DE, Hunt JS. HLA-G1 protein expression is not essential for fetal survival Placenta. 19: 127-132. PMID 9548178 DOI: 10.1016/S0143-4004(98)90000-5  1
1998 Ober C, Hyslop T, Elias S, Weitkamp LR, Hauck WW. Human leukocyte antigen matching and fetal loss: Results of a 10 year prospective study Human Reproduction. 13: 33-38. PMID 9512225 DOI: 10.1093/Humrep/13.1.33  1
1998 Ober C. Do genetics play a role in the pathogenesis of asthma? Journal of Allergy and Clinical Immunology. 101. PMID 9500742 DOI: 10.1016/S0091-6749(98)70234-9  1
1998 Ober C. HLA and pregnancy: The paradox of the fetal allograft American Journal of Human Genetics. 62: 1-5. PMID 9443885 DOI: 10.1086/301692  1
1997 Ober C, Aldrich CL. HLA-G polymorphisms: neutral evolution or novel function? Journal of Reproductive Immunology. 36: 1-21. PMID 9430736 DOI: 10.1016/S0165-0378(97)00062-4  1
1997 Fisfalen ME, Soltani K, Kaplan E, Palmer EM, van Seventer GA, Straus FH, Diaz M, Ober C, DeGroot LJ. Evaluating the role of Th0 and Th1 clones in autoimmune thyroid disease by use of Hu-SCID chimeras. Clinical Immunology and Immunopathology. 85: 253-64. PMID 9400625 DOI: 10.1006/Clin.1997.4431  1
1997 Fisfalen ME, Palmer EM, Van Seventer GA, Soltani K, Sawai Y, Kaplan E, Hidaka Y, Ober C, DeGroot LJ. Thyrotropin-receptor and thyroid peroxidase-specific T cell clones and their cytokine profile in autoimmune thyroid disease. The Journal of Clinical Endocrinology and Metabolism. 82: 3655-63. PMID 9360522 DOI: 10.1210/Jcem.82.11.4336  1
1997 Ober C, Van Der Ven K. Immunogenetics of reproduction: An overview Current Topics in Microbiology and Immunology. 222: 1-23. PMID 9257483 DOI: 10.1007/978-3-642-60614-4_1  1
1997 Marsh DG, Maestri NE, Freidhoff LR, Barnes KC, Togias A, Ehrlich E, Beaty T, Duffy D, Rosenthal R, Imani F, Dunston G, Furbert-Harris P, Malveaux F, Ober C, Cox NJ, et al. A genome-wide search for asthma susceptibility loci in ethnically diverse populations Nature Genetics. 15: 389-392. PMID 9090385 DOI: 10.1038/Ng0497-389  1
1997 Grimsley C, Ober C. Population genetic studies of HLA-E: Evidence for selection Human Immunology. 52: 33-40. PMID 9021407 DOI: 10.1016/S0198-8859(96)00241-8  1
1996 Ober C, Rosinsky B, Grimsley C, van der Ven K, Robertson A, Runge A. Population genetic studies of HLA-G: allele frequencies and linkage disequilibrium with HLA-A1. Journal of Reproductive Immunology. 32: 111-23. PMID 9023816 DOI: 10.1016/S0165-0378(96)01000-5  1
1996 Van Der Ven K, Messer L, Van Der Ven H, Jeyendran RS, Ober C. Cystic fibrosis mutation screening in healthy men with reduced sperm quality Human Reproduction. 11: 513-517. PMID 8671256 DOI: 10.1093/HUMREP/11.3.513  1
1995 Ober C. Current topic: HLA and reproduction: Lessons from studies in the Hutterites Placenta. 16: 569-577. PMID 8577656 DOI: 10.1016/0143-4004(95)90026-8  1
1995 Geppert EF, Lester LA, Ober C. Prioritizing asthma research: the need to investigate childhood asthma. American Journal of Respiratory and Critical Care Medicine. 151: 1294-5. PMID 7735577 DOI: 10.1164/ajrccm.151.5.7735577  1
1993 Margulis SW, Altmann J, Ober C. Sex-biased lactational duration in a human population and its reproductive costs. Behavioral Ecology and Sociobiology. 32: 41-5. PMID 12286204 DOI: 10.1007/Bf00172221  1
1993 Stoffel M, Bell KL, Blackburn CL, Powell KL, Seo TS, Takeda J, Vionnet N, Xiang KS, Gidh-Jain M, Pilkis SJ. Identification of glucokinase mutations in subjects with gestational diabetes mellitus. Diabetes. 42: 937-40. PMID 8495817 DOI: 10.2337/Diab.42.6.937  1
1993 Kostyu DD, Dawson DV, Elias S, Ober C. Deficit of HLA homozygotes in a Caucasian isolate Human Immunology. 37: 135-142. PMID 8244776 DOI: 10.1016/0198-8859(93)90178-4  1
1993 Streck T, van der Ven K, Beer EA, Ober C. Kompatibilität in HLA-DQA1 und HLA-DQB1 Allelen zwischen Mutter und Fetus ist kein zusätzlicher Risikofaktor bei idiopatischen wiederholten Aborten Archives of Gynecology and Obstetrics. 254: 1298-1300. DOI: 10.1007/BF02266403  1
1993 Alberts SC, Ober C. Genetic variability in the major histocompatibility complex: A review of non-pathogen-mediated selective mechanisms American Journal of Physical Anthropology. 92: 71-89. DOI: 10.1002/Ajpa.1330360606  1
1991 Reed AM, Pachman L, Ober C. Molecular genetic studies of major histocompatibility complex genes in children with Juvenile dermatomyositis: Increased risk associated with HLA-DQA1*0501 Human Immunology. 32: 235-240. PMID 1783570 DOI: 10.1016/0198-8859(91)90085-N  1
1989 Ober C, Xiang KS, Thisted RA, Indovina KA, Wason CJ, Dooley S. Increased risk for gestational diabetes mellitus associated with insulin receptor and insulin-like growth factor II restriction fragment length polymorphisms Genetic Epidemiology. 6: 559-569. PMID 2574127 DOI: 10.1002/GEPI.1370060502  1
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