Human Heredity, 1423-0062

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  1. 2013
  2. TFAP2B-Dietary protein and glycemic index interactions and weight maintenance after weight loss in the diogenes trial

    Tanja Stocks, Lars Ängquist, Jörg Hager, Celine Charon, Claus Holst, J. Alfredo Martinez, Wim H.M. Saris, Arne Astrup, Thorkild I.A. Sørensen & Lesli H. Larsen, 2013 Jan 1, In: Human Heredity. 75, 2-4, p. 213-219 7 p.

    Research output: Contribution to journalArticle

  3. Gene × environment interactions in obesity: the state of the evidence.

    Shafqat Ahmad, Tibor V Varga & Paul Franks, 2013, In: Human Heredity. 75, 2-4, p. 106-115

    Research output: Contribution to journalArticle

  4. Recombination promotes canalization against deleterious mutations

    Bengt Olle Bengtsson, 2013, In: Human Heredity. 76, p. 96-96

    Research output: Contribution to journalPublished meeting abstract

  5. 2011
  6. Comparison of Six Statistics of Genetic Association Regarding Their Ability to Discriminate between Causal Variants and Genetically Linked Markers

    Justo Lorenzo Bermejo, Alfonso Garcia Perez, Andreas Brandt, Kari Hemminki & Abigail G. Matthews, 2011, In: Human Heredity. 72, 2, p. 142-152

    Research output: Contribution to journalArticle

  7. 2009
  8. Mother's Genome or Maternally-Inherited Genes Acting in the Fetus Influence Gestational Age in Familial Preterm Birth

    Jevon Plunkett, Mary F. Feitosa, Michelle Trusgnich, Michael F. Wangler, Lisanne Palomar, Zachary A. -F. Kistka, Emily A. DeFranco, Tammy T. Shen, Adrienne E. D. Stormo, Hilkka Puttonen, Mikko Hallman, Ritva Haataja, Aino Luukkonen, Vineta Fellman, Leena Peltonen, Aarno Palotie, E. Warwick Daw, Ping An, Kari Teramo, Ingrid Borecki & 1 others, Louis J. Muglia, 2009, In: Human Heredity. 68, 3, p. 209-219

    Research output: Contribution to journalArticle

  9. 2008
  10. Strategies for Conditional Two-Locus Nonparametric Linkage Analysis.

    Lars Ängquist, Ola Hössjer & Leif Groop, 2008, In: Human Heredity. 66, 3, p. 138-156

    Research output: Contribution to journalArticle

  11. 2005
  12. Detecting Deletions in Families Affected by a Dominant Disease by Use of Marker Data.

    Anna Johansson, Christer Halldén & Torbjörn Säll, 2005, In: Human Heredity. 60, 1, p. 26-35

    Research output: Contribution to journalArticle

  13. 2004
  14. On computation of p-values in parametric linkage analysis

    Azra Kurbasic & O Hossjer, 2004, In: Human Heredity. 57, 4, p. 207-219

    Research output: Contribution to journalArticle

  15. 2003
  16. Polymorphisms of the HDL receptor gene associated with HDL cholesterol levels in diabetic kindred from three populations

    JJ McCarthy, S Lewitzky, C Reeves, A Permutt, B Glaser, Leif Groop, T Lehner & JM Meyer, 2003, In: Human Heredity. 55, 4, p. 163-170

    Research output: Contribution to journalArticle

  17. 1991
  18. Population genetics of the Malmö polymorphism of coagulation factor IX

    Anders Wallmark, Glenna Kunkel, Hassan Mouhli, John Bosco, Rolf Ljung, Inga Marie Nilsson & John B. Graham, 1991, In: Human Heredity. 41, 6, p. 391-396

    Research output: Contribution to journalArticle

  19. 1979
  20. A new N-acetyl-beta-D-hexosaminidase disease with late onset of progressive neurological symptoms

    Alan Chester, B Hultberg, Hans Liedholm & P A Ockerman, 1979, In: Human Heredity. 29, 2, p. 124-128

    Research output: Contribution to journalArticle