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Page 1
Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwide.
Moorthie S, Blencowe H, Darlison MW, Lawn J, Morris JK, Modell B; Congenital Disorders Expert Group; Bittles AH, Blencowe H, Christianson A, Cousens S, Darlison MW, Gibbons S, Hamamy H, Khoshnood B, Howson CP, Lawn J, Mastroiacovo P, Modell B, Moorthie S, Morris JK, Mossey PA, Neville AJ, Petrou M, Povey S, Rankin J, Schuler-Faccini L, Wren C, Yunnis KA. Moorthie S, et al. Among authors: rankin j. J Community Genet. 2018 Oct;9(4):387-396. doi: 10.1007/s12687-018-0384-2. Epub 2018 Sep 14. J Community Genet. 2018. PMID: 30218347 Free PMC article.
Birth prevalence and survival of exomphalos in england and wales: 2005 to 2011.
Springett A, Draper ES, Rankin J, Rounding C, Tucker D, Stoianova S, Wellesley D, Morris JK. Springett A, et al. Among authors: rankin j. Birth Defects Res A Clin Mol Teratol. 2014 Sep;100(9):721-5. doi: 10.1002/bdra.23301. Epub 2014 Sep 1. Birth Defects Res A Clin Mol Teratol. 2014. PMID: 25178262
Major congenital anomalies in babies born with Down syndrome: a EUROCAT population-based registry study.
Morris JK, Garne E, Wellesley D, Addor MC, Arriola L, Barisic I, Beres J, Bianchi F, Budd J, Dias CM, Gatt M, Klungsoyr K, Khoshnood B, Latos-Bielenska A, Mullaney C, Nelen V, Neville AJ, O'Mahony M, Queisser-Luft A, Randrianaivo H, Rankin J, Rissmann A, Rounding C, Sipek A, Stoianova S, Tucker D, de Walle H, Yevtushok L, Loane M, Dolk H. Morris JK, et al. Among authors: rankin j. Am J Med Genet A. 2014 Dec;164A(12):2979-86. doi: 10.1002/ajmg.a.36780. Epub 2014 Sep 24. Am J Med Genet A. 2014. PMID: 25257471
The Association of H1N1 Pandemic Influenza with Congenital Anomaly Prevalence in Europe: An Ecological Time Series Study.
Luteijn JM, Addor MC, Arriola L, Bianchi F, Garne E, Khoshnood B, Nelen V, Neville A, Queisser-Luft A, Rankin J, Rounding C, Verellen-Dumoulin C, de Walle H, Wellesley D, Wreyford B, Yevtushok L, de Jong-van den Berg L, Morris J, Dolk H. Luteijn JM, et al. Among authors: rankin j. Epidemiology. 2015 Nov;26(6):853-61. doi: 10.1097/EDE.0000000000000372. Epidemiology. 2015. PMID: 26327589
Congenital anomalies associated with trisomy 18 or trisomy 13: A registry-based study in 16 European countries, 2000-2011.
Springett A, Wellesley D, Greenlees R, Loane M, Addor MC, Arriola L, Bergman J, Cavero-Carbonell C, Csaky-Szunyogh M, Draper ES, Garne E, Gatt M, Haeusler M, Khoshnood B, Klungsoyr K, Lynch C, Dias CM, McDonnell R, Nelen V, O'Mahony M, Pierini A, Queisser-Luft A, Rankin J, Rissmann A, Rounding C, Stoianova S, Tuckerz D, Zymak-Zakutnia N, Morris JK. Springett A, et al. Among authors: rankin j. Am J Med Genet A. 2015 Dec;167A(12):3062-9. doi: 10.1002/ajmg.a.37355. Epub 2015 Sep 8. Am J Med Genet A. 2015. PMID: 26347425
Use of hierarchical models to analyze European trends in congenital anomaly prevalence.
Cavadino A, Prieto-Merino D, Addor MC, Arriola L, Bianchi F, Draper E, Garne E, Greenlees R, Haeusler M, Khoshnood B, Kurinczuk J, McDonnell B, Nelen V, O'Mahony M, Randrianaivo H, Rankin J, Rissmann A, Tucker D, Verellen-Dumoulin C, de Walle H, Wellesley D, Morris JK. Cavadino A, et al. Among authors: rankin j. Birth Defects Res A Clin Mol Teratol. 2016 Jun;106(6):480-8. doi: 10.1002/bdra.23515. Birth Defects Res A Clin Mol Teratol. 2016. PMID: 27301561
Prevalence of microcephaly in Europe: population based study.
Morris JK, Rankin J, Garne E, Loane M, Greenlees R, Addor MC, Arriola L, Barisic I, Bergman JE, Csaky-Szunyogh M, Dias C, Draper ES, Gatt M, Khoshnood B, Klungsoyr K, Kurinczuk JJ, Lynch C, McDonnell R, Nelen V, Neville AJ, O'Mahony MT, Pierini A, Randrianaivo H, Rissmann A, Tucker D, Verellen-Dumoulin C, de Walle HE, Wellesley D, Wiesel A, Dolk H. Morris JK, et al. Among authors: rankin j. BMJ. 2016 Sep 13;354:i4721. doi: 10.1136/bmj.i4721. BMJ. 2016. PMID: 27623840 Free PMC article.
A sustainable solution for the activities of the European network for surveillance of congenital anomalies: EUROCAT as part of the EU Platform on Rare Diseases Registration.
Kinsner-Ovaskainen A, Lanzoni M, Garne E, Loane M, Morris J, Neville A, Nicholl C, Rankin J, Rissmann A, Tucker D, Martin S. Kinsner-Ovaskainen A, et al. Among authors: rankin j. Eur J Med Genet. 2018 Sep;61(9):513-517. doi: 10.1016/j.ejmg.2018.03.008. Epub 2018 Mar 27. Eur J Med Genet. 2018. PMID: 29597096 Free article. Review.
Trends in congenital anomalies in Europe from 1980 to 2012.
Morris JK, Springett AL, Greenlees R, Loane M, Addor MC, Arriola L, Barisic I, Bergman JEH, Csaky-Szunyogh M, Dias C, Draper ES, Garne E, Gatt M, Khoshnood B, Klungsoyr K, Lynch C, McDonnell R, Nelen V, Neville AJ, O'Mahony M, Pierini A, Queisser-Luft A, Randrianaivo H, Rankin J, Rissmann A, Kurinczuk J, Tucker D, Verellen-Dumoulin C, Wellesley D, Dolk H. Morris JK, et al. Among authors: rankin j. PLoS One. 2018 Apr 5;13(4):e0194986. doi: 10.1371/journal.pone.0194986. eCollection 2018. PLoS One. 2018. PMID: 29621304 Free PMC article.
EUROCAT: an update on its functions and activities.
Tucker FD, Morris JK; JRC Management Committee; Neville A, Garne E, Kinsner-Ovaskainen A, Lanzoni M, Loane MA, Martin S, Nicholl C, Rankin J, Rissmann AK. Tucker FD, et al. Among authors: rankin j. J Community Genet. 2018 Oct;9(4):407-410. doi: 10.1007/s12687-018-0367-3. Epub 2018 May 7. J Community Genet. 2018. PMID: 29736796 Free PMC article.
1,600 results