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Superfund Research Program

American Journal of Human Genetics (impact factor: 11.025)



  • Lee S, Abecasis GR, Boehnke M, Lin X. 2014. Rare-variant association analysis: study designs and statistical tests. Am J Hum Genet 95(1):5-23. doi:10.1016/j.ajhg.2014.06.009 PMID:24995866 PMCID:PMC4085641
  • Skibola CF, Berndt SI, Vijai J, Conde L, Wang Z, Yeager M, de Bakker PI, Birmann BM, Vajdic CM, Lightfoot TJ, Foo J, Bracci PM, Vermeulen R, Slager SL, de Sanjose S, Wang SS, Linet MS, Salles G, Lan Q, Severi G, Hjalgrim H, Melbye M, Gu J, Ghesquieres H, Link BK, Morton LM, Holly EA, Smith A, Tinker LF, Teras LR, Kricker A, Becker N, Purdue MP, Spinelli JJ, Zhang Y, Giles GG, Vineis P, Monnereau A, Bertrand KA, Albanes D, Zeleniuch-Jacquotte A, Gabbas A, Chung CC, Burdett L, Hutchinson A, Lawrence C, Montalvan R, Liang L, Huang J, Ma B, Liu J, Adami H, Glimelius B, Ye Y, Nowakowski GS, Dogan A, Thompson CA, Habermann TM, Novak AJ, Liebow M, Witzig TE, Weiner GJ, Schenker MB, Hartge P, De Roos AJ, Cozen W, Zhi D, Akers NK, Riby J, Smith MT, Lacher M, Villano DJ, Maria A, Roman E, Kane E, Jackson RD, North KE, Diver WR, Turner J, Armstrong BK, Benavente Y, Boffetta P, Brennan P, Foretova L, Maynadie M, Staines A, McKay J, Brooks-Wilson AR, Zheng T, Holford TR, Kaaks R, Kelly RS, Ohlsson B, Travis RC, Weiderpass E, Clavel J, Giovannucci E, Kraft P, Virtamo J, Mazza P, Cocco P, Ennas M, Chiu BC, Fraumeni JF, Nieters A, Offit K, Wu X, Cerhan JR, Smedby KE, Chanock SJ, Rothman N. 2014. Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region. Am J Hum Genet 95(4):462-471. doi:10.1016/j.ajhg.2014.09.004 PMID:25279986 PMCID:PMC4185120


  • Franceschini N, Fox E, Zhang Z, Edwards TL, Nalls MA. 2013. Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. Am J Hum Genet 93:545-554. doi:10.1016/j.ajhg.2013.07.010 PMID:23972371 PMCID:PMC3769920


  • Lee S, Emond MJ, Bamshad MJ, Barnes KC, Rieder MJ, Nickerson DA, Christiani DC, Wurfel MM, Lin X. 2012. Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies. Am J Hum Genet 91(2):224-237. doi:10.1016/j.ajhg.2012.06.007 PMID:22863193 PMCID:PMC3415556



  • Glaser RL, Broman KW, Schulman RL, Eskenazi B, Wyrobek AJ, Jabs EW. 2003. The paternal-age effect in Apert syndrome is due, in part, to the increased frequency of mutations in sperm. Am J Hum Genet 73(4):939-947. PMID:12900791


  • Rubes J, Vozdova M, Robbins WA, Rezacova O, Perreault SD, Wyrobek AJ. 2002. Stable variants of sperm aneuploidy among healthy men show associations between germinal and somatic aneuploidy. Am J Hum Genet 70(6):1507-1519. PMID:11992257


  • Lowe X, Eskenazi B, Nelson DO, Kidd SA, Alme A, Wyrobek AJ. 2001. Frequency of XY sperm increases with age in fathers of boys with Klinefelter syndrome. Am J Hum Genet 69(5):1046-1054. PMID:11582569


  • Sloter E, Nath J, Wyrobek AJ. 1999. Correlation between numerical and structural chromosome damage in sperm from 13 healthy men using multicolor FISH. Am J Hum Genet 65(4):A357.


  • Lowe X, Eskenazi B, Kidd SA, Alme A, Weisiger K, Aylstock M, Nelson DE, Wyrobek AJ. 1998. Sperm disomy 21 is associated with sex chromosomal aneuploidies but does not preferentially segregate with the Y chromosome: a study of 38 healthy fertile men. Am J Hum Genet 63(4):A143.
  • Sloter E, Lowe X, Nath J, Wyrobek AJ. 1998. A novel multi-color FISH method for human sperm demonstrates that post-meiotic chromosome breaks occur more frequently than duplications and deletions. Am J Hum Genet 63(4):A150.


  • Wiencke JK, Spitz MR, McMillan A, Kelsey KT. 1996. Lung cancer in Mexican-American and African-Americans is associated with the wildtype genotype of the NAD(P)H:quinone oxidoreductase polymorphism. Am J Hum Genet 59:A294.
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