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

Year Number of Results
1979 3
1981 2
1982 3
1983 4
1984 1
1985 3
1986 3
1987 2
1988 8
1989 6
1990 5
1991 6
1992 6
1993 9
1994 5
1995 7
1996 3
1997 5
1998 2
1999 4
2000 2
2001 2
2002 1
2003 2
2005 3
2006 4
2007 1
2008 5
2009 3
2010 3
2011 5
2012 3
2013 2
2020 1
2021 1
2022 1
2023 1
2024 1

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126 results

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Page 1
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death.
Byrne AB, Arts P, Ha TT, Kassahn KS, Pais LS, O'Donnell-Luria A; Broad Institute Center for Mendelian Genomics; Babic M, Frank MSB, Feng J, Wang P, Lawrence DM, Eshraghi L, Arriola L, Toubia J, Nguyen H; Genomic Autopsy Study Research Network; McGillivray G, Pinner J, McKenzie F, Morrow R, Lipsett J, Manton N, Khong TY, Moore L, Liebelt JE, Schreiber AW, King-Smith SL, Hardy TSE, Jackson MR, Barnett CP, Scott HS. Byrne AB, et al. Nat Med. 2023 Jan;29(1):180-189. doi: 10.1038/s41591-022-02142-1. Epub 2023 Jan 19. Nat Med. 2023. PMID: 36658419 Free PMC article.
Congenital heart malformation in Yunis-Varón syndrome.
Adès LC, Morris LL, Richardson M, Pearson C, Haan EA. Adès LC, et al. Among authors: haan ea. J Med Genet. 1993 Sep;30(9):788-92. doi: 10.1136/jmg.30.9.788. J Med Genet. 1993. PMID: 8411078 Free PMC article. Review.
CP or not CP? A review of diagnoses in a cerebral palsy register.
Zarrinkalam R, Russo RN, Gibson CS, van Essen P, Peek AK, Haan EA. Zarrinkalam R, et al. Among authors: haan ea. Pediatr Neurol. 2010 Mar;42(3):177-80. doi: 10.1016/j.pediatrneurol.2009.09.001. Pediatr Neurol. 2010. PMID: 20159426 Review.
The genomic basis of cerebral palsy: a HuGE systematic literature review.
O'Callaghan ME, MacLennan AH, Haan EA, Dekker G; South Australian Cerebral Palsy Research Group. O'Callaghan ME, et al. Among authors: haan ea. Hum Genet. 2009 Jul;126(1):149-72. doi: 10.1007/s00439-009-0638-5. Epub 2009 Feb 24. Hum Genet. 2009. PMID: 19238444 Review.
Author Correction: Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death.
Byrne AB, Arts P, Ha TT, Kassahn KS, Pais LS, O'Donnell-Luria A; Broad Institute Center for Mendelian Genomics; Babic M, Frank MSB, Feng J, Wang P, Lawrence DM, Eshraghi L, Arriola L, Toubia J, Nguyen H; Genomic Autopsy Study Research Network; McGillivray G, Pinner J, McKenzie F, Morrow R, Lipsett J, Manton N, Khong TY, Moore L, Liebelt JE, Schreiber AW, King-Smith SL, Hardy TSE, Jackson MR, Barnett CP, Scott HS. Byrne AB, et al. Nat Med. 2024 Jan;30(1):302. doi: 10.1038/s41591-023-02487-1. Nat Med. 2024. PMID: 37429925 No abstract available.
Epidemiologic associations with cerebral palsy.
O'Callaghan ME, MacLennan AH, Gibson CS, McMichael GL, Haan EA, Broadbent JL, Goldwater PN, Dekker GA; Australian Collaborative Cerebral Palsy Research Group. O'Callaghan ME, et al. Among authors: haan ea. Obstet Gynecol. 2011 Sep;118(3):576-582. doi: 10.1097/AOG.0b013e31822ad2dc. Obstet Gynecol. 2011. PMID: 21860286
Homozygotes for FRA16B are normal.
Hocking T, Feichtinger W, Schmid M, Haan EA, Baker E, Sutherland GR. Hocking T, et al. Among authors: haan ea. Chromosome Res. 1999;7(7):553-6. doi: 10.1023/a:1009293613064. Chromosome Res. 1999. PMID: 10598570
126 results