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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2005 2
2006 4
2007 6
2008 4
2009 2
2010 3
2011 7
2012 7
2013 3
2014 6
2015 5
2016 3
2017 2
2019 1
2020 1
2021 2
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47 results
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Page 1
Neuron-Derived Neurotrophic Factor Is Mutated in Congenital Hypogonadotropic Hypogonadism.
Messina A, Pulli K, Santini S, Acierno J, Känsäkoski J, Cassatella D, Xu C, Casoni F, Malone SA, Ternier G, Conte D, Sidis Y, Tommiska J, Vaaralahti K, Dwyer A, Gothilf Y, Merlo GR, Santoni F, Niederländer NJ, Giacobini P, Raivio T, Pitteloud N. Messina A, et al. Among authors: tommiska j. Am J Hum Genet. 2020 Jan 2;106(1):58-70. doi: 10.1016/j.ajhg.2019.12.003. Epub 2019 Dec 26. Am J Hum Genet. 2020. PMID: 31883645 Free PMC article.
53BP1 loss rescues BRCA1 deficiency and is associated with triple-negative and BRCA-mutated breast cancers.
Bouwman P, Aly A, Escandell JM, Pieterse M, Bartkova J, van der Gulden H, Hiddingh S, Thanasoula M, Kulkarni A, Yang Q, Haffty BG, Tommiska J, Blomqvist C, Drapkin R, Adams DJ, Nevanlinna H, Bartek J, Tarsounas M, Ganesan S, Jonkers J. Bouwman P, et al. Among authors: tommiska j. Nat Struct Mol Biol. 2010 Jun;17(6):688-95. doi: 10.1038/nsmb.1831. Epub 2010 May 9. Nat Struct Mol Biol. 2010. PMID: 20453858 Free PMC article.
Gonadotropin-releasing hormone receptor mutations in ageing men.
Tommiska J, Känsäkoski J, Pitteloud N, Wu F, Raivio T. Tommiska J, et al. Clin Endocrinol (Oxf). 2016 Jan;84(1):150-1. doi: 10.1111/cen.12833. Epub 2015 Jul 1. Clin Endocrinol (Oxf). 2016. PMID: 26044071 No abstract available.
Genetic Overlap between Holoprosencephaly and Kallmann Syndrome.
Vaaralahti K, Raivio T, Koivu R, Valanne L, Laitinen EM, Tommiska J. Vaaralahti K, et al. Among authors: tommiska j. Mol Syndromol. 2012 Jun;3(1):1-5. doi: 10.1159/000338706. Epub 2012 May 16. Mol Syndromol. 2012. PMID: 22855648 Free PMC article.
Genetics of congenital hypogonadotropic hypogonadism in Denmark.
Tommiska J, Känsäkoski J, Christiansen P, Jørgensen N, Lawaetz JG, Juul A, Raivio T. Tommiska J, et al. Eur J Med Genet. 2014 Jul;57(7):345-8. doi: 10.1016/j.ejmg.2014.04.002. Epub 2014 Apr 13. Eur J Med Genet. 2014. PMID: 24732674
LIN28B in constitutional delay of growth and puberty.
Tommiska J, Wehkalampi K, Vaaralahti K, Laitinen EM, Raivio T, Dunkel L. Tommiska J, et al. J Clin Endocrinol Metab. 2010 Jun;95(6):3063-6. doi: 10.1210/jc.2009-2344. Epub 2010 Mar 29. J Clin Endocrinol Metab. 2010. PMID: 20350940
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