Publications (876)
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Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe
Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe
Barisic I, Boban L, Akhmedzhanova D, Bergman JEH, Cavero-Carbonell C, Grinfelde I, Materna-Kiryluk A, Latos-Bielenska A, Randrianaivo H, Zymak-Zakutnya N, Sansovic I, Lanzoni M, Morris JK
Eur J Med Genet., 2018 , Sep;61(9): 499 - 507
Subjects: somatic overgrowth, macroglossia, abdominal wall defects, neonatal hypoglycemia, and predisposition to embryonal tumors
Anomalies: Beckwith Wiedemann syndrome; Congenital anomalies; Epidemiology; Europe; Prenatal diagnosis -
Beta-blocker use in pregnancy and risk of specific congenital anomalies: a European case-malformed control study
Beta-blocker use in pregnancy and risk of specific congenital anomalies: a European case-malformed control study
Bergman JEH, Lutke LR, Gans ROB, Addor MC, Barisic I, Cavero-Carbonell C, Garne E, Gatt M, Klungsoyr K, Lelong N, Lynch C, Mokoroa O, Nelen V, Neville AJ, Pierini A, Randrianaivo H, Rissmann A, Tucker D, Wiesel A, Dolk H, Loane M, Bakker MK
Drug Saf. , 2018 , 41: (4) 415 - 427
Subjects: chronic hypertension , beta-blockers, pregnancy
Anomalies: congenital anomalies -
Effectiveness of 12-13-week scan for early diagnosis of fetal congenital anomalies in the cell-free DNA era
Effectiveness of 12-13-week scan for early diagnosis of fetal congenital anomalies in the cell-free DNA era
Kenkhuis MJA, Bakker M, Bardi F, Fontanella F, Bakker MK, Fleurke-Rozema JH, Bilardo
Ultrasound Obstet Gynecol. , 2018 , 51: (4) 463 - 469
Subjects: fetal congenital anomalies, cell-free DNA
Anomalies: congenital anomalies -
Environmental and individual exposure and the risk of congenital anomalies: a review of recent epidemiological evidence
Environmental and individual exposure and the risk of congenital anomalies: a review of recent epidemiological evidence
Baldacci S, Gorini F, Santoro M, Pierini A, Minichilli F, Bianchi F
Epidemiologia e Prevenzione, 2018 , 42: (3-4 Suppl 1) 1 - 34
Subjects: prevention; non-genetic risk factors
Anomalies: major subgroups of congenital anomalies -
Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age - A EUROCAT study.
Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age - A EUROCAT study.
Garne E, Rissmann A, Addor MC, Barisic I, Bergman J, Braz P, Cavero-Carbonell C, Draper ES, Gatt M, Haeusler M, Klungsoyr K, Kurinczuk JJ, Lelong N, Luyt K, Lynch C, O'Mahony MT, Mokoroa O, Nelen V, Neville AJ, Pierini A, Randrianaivo H, Rankin J, Rouget F, Schaub B, Tucker D, Verellen-Dumoulin C, Wellesley D, Wiesel A, Zymak-Zakutnia N, Lanzoni M, Morris JK
Eur J Med Genet., 2018 , 61: (9) 483 - 488
Subjects: associated anomalies, eurocat, maternal age, population based, prevalence, septo-optic dysplasia
Anomalies: septo-optic nerve dysplasia, congenital anomalies -
Estimating global burden of disease due to congenital anomaly: an analysis of European data
Estimating global burden of disease due to congenital anomaly: an analysis of European data
Boyle B, Addor MC, Arriola L, Barisic I, Bianchi F, Csáky-Szunyogh M, de Walle HEK, Dias CM, Draper E, Gatt M, Garne E, Haeusler M, Källén K, Latos-Bielenska A, McDonnell B, Mullaney C, Nelen V, Neville AJ, O'Mahony M, Queisser-Wahrendorf A, Randrianaivo H, Rankin J, Rissmann A, Ritvanen A, Rounding C, Tucker D, Verellen-Dumoulin C, Wellesley D, Wreyford B, Zymak-Zakutnia N, Dolk H
Arch Dis Child Fetal Neonatal, 2018 , 103(1): F22 - F28
Subjects: Congenital anomaly; DALY; Global Burden of Disease; YLL; mortality
Anomalies: congenital anomaly -
Insulin analogues use in pregnancy among women with pregestational diabetes mellitus and risk of congenital anomaly: a retrospective population-based cohort study
Insulin analogues use in pregnancy among women with pregestational diabetes mellitus and risk of congenital anomaly: a retrospective population-based cohort study
Wang H, Wender-Ozegowska E, Garne E, Morgan M, Loane M, Morris JK, Bakker MK, Gatt M, de Walle H, Jordan S, Materna-Kiryluk A, Nelen V, Thys G, Wiesel A, Dolk H, de Jong-van den Berg LTW
BMJ open. , 2018 , 8(2): (e014972)
Subjects: diabetes in pregnancy, epidemiology, maternal medicine, risk of major congenital anomalies, congenital heart defects
Anomalies: congenital anomalies, -
Metformin exposure in the first trimester of pregnancy and the risk of all or specific congenital anomalies: an exploratory case-control study
Metformin exposure in the first trimester of pregnancy and the risk of all or specific congenital anomalies: an exploratory case-control study
Joanne E Given, Maria Loane, Ester Garne, Marie-Claude Addor, Marian Bakker, Bénédicte Bertaut-Nativel, Miriam Gatt, Kari Klungsoyr, Nathalie Lelong, Margery Morgan, Amanda J Neville, Anna Pierini, Anke Rissmann, Helen Dolk
BMJ, 2018 , Jun 25;361:k2477:
Subjects: exposure to metformin
Anomalies: congenital anomalies -
Prenatal diagnosis of urinary tract anomalies, a cohort study in the Northern Netherlands
Prenatal diagnosis of urinary tract anomalies, a cohort study in the Northern Netherlands
Bakker MK, Bergman JEH, Fleurke-Rozema H, Streefland E, Gracchi V, Bilardo CM, de Walle HEK
Prenat Diagn. , 2018 , 38: (2) 130 - 134
Subjects: anomaly scan, urinary tract (UT) anomalies
Anomalies: urinary tract (UT) anomalies -
Prevalence of valproate syndrome in Europe from 2005 to 2014: A registry based multi-centre study
Prevalence of valproate syndrome in Europe from 2005 to 2014: A registry based multi-centre study
Morris JK, Garne E, Loane M, Addor MC, Barisic I, Bianchi F, Gatt M, Lanzoni M, Lynch C, Mokoroa O,
Nelen V, Neville A, O'Mahony MT, Randrianaivo-Ranjatoelina H, Rissmann A,Tucker D, de Walle HEK, Zymak-Zakutnia N, Rankin J
Eur J Med Genet , 2018 , Sep;61: (9) 479 - 482
Subjects: Congenital anomaly; Sodium valproate; Valproic acid
Anomalies: Congenital anomaly