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maurizio clementi
maurizio clementi
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Title
Cited by
Cited by
Year
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
13682018
Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders
PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ...
Cell 179 (7), 1469-1482. e11, 2019
10302019
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa
HJ Watson, Z Yilmaz, LM Thornton, C Hübel, JRI Coleman, HA Gaspar, ...
Nature genetics 51 (8), 1207-1214, 2019
7812019
Anti-inflammatory and immunosuppressive drugs and reproduction
M Østensen, M Khamashta, M Lockshin, A Parke, A Brucato, H Carp, ...
Arthritis research & therapy 8, 1-19, 2006
6752006
Genetic control of the CD4/CD8 T-cell ratio in humans
A Amadori, R Zamarchi, G De Silvestro, G Forza, G Cavatton, GA Danieli, ...
Nature medicine 1 (12), 1279-1283, 1995
5151995
Evaluation of prenatal diagnosis of congenital heart diseases by ultrasound: experience from 20 European registries
E Garne, C Stoll, M Clementi
Ultrasound in Obstetrics and Gynecology: The Official Journal of the …, 2001
4402001
A genome-wide association study of anorexia nervosa
V Boraska, CS Franklin, JAB Floyd, LM Thornton, LM Huckins, L Southam, ...
Molecular psychiatry 19 (10), 1085-1094, 2014
3412014
Prenatal detection of congenital renal malformations by fetal ultrasonographic examination: an analysis of 709,030 births in 12 European countries
A Wiesel, A Queisser-Luft, M Clementi, S Bianca, C Stoll, ...
European journal of medical genetics 48 (2), 131-144, 2005
3382005
Evaluation of prenatal ultrasound diagnosis of fetal abdominal wall defects by 19 European registries
I Barisic, M Clementi, M Haeusler, R Gjergja, J Kern, C Stoll
Ultrasound in Obstetrics and Gynecology: The Official Journal of the …, 2001
2912001
Congenital diaphragmatic hernia: evaluation of prenatal diagnosis in 20 European regions
E Garne, M Haeusler, I Barisic, R Gjergja, C Stoll, M Clementi
Ultrasound in Obstetrics and Gynecology: The Official Journal of the …, 2002
2882002
Searching for psoriasis susceptibility genes in Italy: genome scan and evidence for a new locus on chromosome 1
F Capon, G Novelli, S Semprini, M Clementi, M Nudo, P Vultaggio, ...
Journal of Investigative Dermatology 112 (1), 32-35, 1999
2671999
Vitamin K antagonists and pregnancy outcome
C Schaefer, D Hannemann, R Meister, E Eléfant, W Paulus, T Vial, ...
Thrombosis and haemostasis 95 (06), 949-957, 2006
2662006
Paroxetine and fluoxetine in pregnancy: a prospective, multicentre, controlled, observational study
O Diav‐Citrin, S Shechtman, D Weinbaum, R Wajnberg, M Avgil, ...
British journal of clinical pharmacology 66 (5), 695-705, 2008
2552008
Methimazole embryopathy: delineation of the phenotype
M Clementi, E Di Gianantonio, E Pelo, I Mammi, RT Basile, R Tenconi
American journal of medical genetics 83 (1), 43-46, 1999
2491999
Adverse effects of prenatal methimazole exposure
E Di Gianantonio, C Schaefer, PP Mastroiacovo, MP Cournot, ...
Teratology 64 (5), 262-266, 2001
2312001
Pregnancy outcome of women exposed to azathioprine during pregnancy
LH Goldstein, G Dolinsky, R Greenberg, C Schaefer, R Cohen‐Kerem, ...
Birth Defects Research Part A: Clinical and Molecular Teratology 79 (10 …, 2007
2292007
Teratogenicity of mycophenolate confirmed in a prospective study of the European Network of Teratology Information Services
M Hoeltzenbein, E Elefant, T Vial, V Finkel‐Pekarsky, S Stephens, ...
American journal of medical genetics Part A 158 (3), 588-596, 2012
2252012
Conjoined twins: a worldwide collaborative epidemiological study of the International Clearinghouse for Birth Defects Surveillance and Research
OM Mutchinick, L Luna‐Muñoz, E Amar, MK Bakker, M Clementi, ...
American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2011
2162011
Evaluation of prenatal diagnosis of cleft lip with or without cleft palate and cleft palate by ultrasound: experience from 20 European registries
M Clementi, R Tenconi, F Bianchi, C Stoll, EUROSCAN Study Group
Prenatal diagnosis 20 (11), 870-875, 2000
2152000
Identification of a SUFU germline mutation in a family with Gorlin syndrome
L Pastorino, P Ghiorzo, S Nasti, L Battistuzzi, R Cusano, C Marzocchi, ...
American journal of medical genetics Part A 149 (7), 1539-1543, 2009
2142009
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