| Year |
Citation |
Score |
| 2019 |
Cassina M, Leon FF, Ruol M, Chiarenza SF, Scirè G, Midrio P, Clementi M, Gamba P. Prevalence and survival of patients with anorectal malformations: A population-based study. Journal of Pediatric Surgery. 54: 1998-2003. PMID 30935729 DOI: 10.1016/J.Jpedsurg.2019.03.004 |
0.309 |
|
| 2019 |
Trevisson E, Morbidoni V, Forzan M, Daolio C, Fumini V, Parrozzani R, Cassina M, Midena E, Salviati L, Clementi M. The Arg1038Gly missense variant in the NF1 gene causes a mild phenotype without neurofibromas. Molecular Genetics & Genomic Medicine. e616. PMID 30843352 DOI: 10.1002/mgg3.616 |
0.317 |
|
| 2018 |
Cassina M, Calò A, Salviati L, Alghisi A, Montaldi A, Clementi M. Prenatal detection of trisomy 8 mosaicism: Pregnancy outcome and follow up of a series of 17 consecutive cases. European Journal of Obstetrics & Gynecology and Reproductive Biology. 221: 23-27. PMID 29232625 DOI: 10.1016/J.Ejogrb.2017.12.012 |
0.389 |
|
| 2017 |
Alby C, Boutaud L, Bonnière M, Collardeau-Frachon S, Guibaud L, Lopez E, Bruel AL, Aral B, Sonigo P, Roth P, Vibert-Guigue C, Castaigne V, Carbonne B, Joyé N, Faivre L, ... ... Clementi M, et al. In utero ultrasound diagnosis of corpus callosum agenesis leading to the identification of orofaciodigital type 1 syndrome in female fetuses. Birth Defects Research. PMID 29193896 DOI: 10.1002/Bdr2.1154 |
0.356 |
|
| 2017 |
Trevisson E, Cassina M, Opocher E, Vicenzi V, Lucchetta M, Parrozzani R, Miglionico G, Mardari R, Viscardi E, Midena E, Clementi M. Natural history of optic pathway gliomas in a cohort of unselected patients affected by Neurofibromatosis 1. Journal of Neuro-Oncology. PMID 28577031 DOI: 10.1007/s11060-017-2517-6 |
0.301 |
|
| 2017 |
Cassina M, Cerqua C, Rossi S, Salviati L, Martini A, Clementi M, Trevisson E. A synonymous splicing mutation in the SF3B4 gene segregates in a family with highly variable Nager syndrome. European Journal of Human Genetics. 25: 371-375. PMID 27966544 DOI: 10.1038/Ejhg.2016.176 |
0.354 |
|
| 2017 |
Cassina M, Cagnoli GA, Zuccarello D, Gianantonio ED, Clementi M. Human teratogens and genetic phenocopies. Understanding pathogenesis through human genes mutation. European Journal of Medical Genetics. 60: 22-31. PMID 27639441 DOI: 10.1016/J.Ejmg.2016.09.011 |
0.344 |
|
| 2016 |
Russo S, Calzari L, Mussa A, Mainini E, Cassina M, Di Candia S, Clementi M, Guzzetti S, Tabano S, Miozzo M, Sirchia S, Finelli P, Prontera P, Maitz S, Sorge G, et al. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes. Clinical Epigenetics. 8: 23. PMID 26933465 DOI: 10.1186/s13148-016-0183-8 |
0.347 |
|
| 2016 |
Cassina M, Ruol M, Pertile R, Midrio P, Piffer S, Vicenzi V, Saugo M, Stocco CF, Gamba P, Clementi M. Prevalence, characteristics, and survival of children with esophageal atresia: A 32-year population-based study including 1,417,724 consecutive newborns. Birth Defects Research. Part a, Clinical and Molecular Teratology. PMID 26931365 DOI: 10.1002/bdra.23493 |
0.308 |
|
| 2015 |
Cassina M, Rigon C, Casarin A, Vicenzi V, Salviati L, Clementi M. FBXO28 is a critical gene of the 1q41q42 microdeletion syndrome. American Journal of Medical Genetics. Part A. 167: 1418-20. PMID 25900767 DOI: 10.1002/ajmg.a.37033 |
0.327 |
|
| 2015 |
Winterfeld U, Klinger G, Panchaud A, Stephens S, Arnon J, Malm H, Te Winkel B, Clementi M, Pistelli A, Ma?áková E, Eleftheriou G, Merlob P, Kaplan YC, Buclin T, Rothuizen LE. Pregnancy outcome following maternal exposure to mirtazapine: a multicenter, prospective study. Journal of Clinical Psychopharmacology. 35: 250-9. PMID 25830592 DOI: 10.1097/JCP.0000000000000309 |
0.343 |
|
| 2015 |
Desbats MA, Vetro A, Limongelli I, Lunardi G, Casarin A, Doimo M, Spinazzi M, Angelini C, Cenacchi G, Burlina A, Rodriguez Hernandez MA, Chiandetti L, Clementi M, Trevisson E, Navas P, et al. Primary coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure. European Journal of Human Genetics : Ejhg. PMID 25564041 DOI: 10.1038/ejhg.2014.277 |
0.353 |
|
| 2015 |
Kuechler A, Zink AM, Wieland T, Lüdecke HJ, Cremer K, Salviati L, Magini P, Najafi K, Zweier C, Czeschik JC, Aretz S, Endele S, Tamburrino F, Pinato C, Clementi M, et al. Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome. European Journal of Human Genetics : Ejhg. 23: 753-60. PMID 25138099 DOI: 10.1038/Ejhg.2014.165 |
0.33 |
|
| 2014 |
Cassina M, Donà M, Di Gianantonio E, Litta P, Clementi M. First-trimester exposure to metformin and risk of birth defects: a systematic review and meta-analysis. Human Reproduction Update. 20: 656-69. PMID 24861556 DOI: 10.1093/humupd/dmu022 |
0.356 |
|
| 2014 |
Virzì GM, Bruson A, Corradi V, Gastaldon F, de Cal M, Donà M, Cruz DN, Clementi M, Ronco C. High-resolution melt as a screening method in autosomal dominant polycystic kidney disease (ADPKD). Journal of Clinical Laboratory Analysis. 28: 328-34. PMID 24658975 DOI: 10.1002/jcla.21689 |
0.307 |
|
| 2014 |
Weber-Schoendorfer C, Chambers C, Wacker E, Beghin D, Bernard N, Shechtman S, Johnson D, Cuppers-Maarschalkerweerd B, Pistelli A, Clementi M, Winterfeld U, Eleftheriou G, Pupco A, Kao K, et al. Pregnancy outcome after methotrexate treatment for rheumatic disease prior to or during early pregnancy: a prospective multicenter cohort study. Arthritis & Rheumatology (Hoboken, N.J.). 66: 1101-10. PMID 24470106 DOI: 10.1002/Art.38368 |
0.339 |
|
| 2014 |
Fallerini C, Dosa L, Tita R, Del Prete D, Feriozzi S, Gai G, Clementi M, La Manna A, Miglietti N, Mancini R, Mandrile G, Ghiggeri GM, Piaggio G, Brancati F, Diano L, et al. Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases. Clinical Genetics. 86: 252-7. PMID 24033287 DOI: 10.1111/cge.12258 |
0.33 |
|
| 2014 |
Paul BM, Consugar MB, Ryan Lee M, Sundsbak JL, Heyer CM, Rossetti S, Kubly VJ, Hopp K, Torres VE, Coto E, Clementi M, Bogdanova N, de Almeida E, Bichet DG, Harris PC. Evidence of a third ADPKD locus is not supported by re-analysis of designated PKD3 families. Kidney International. 85: 383-92. PMID 23760289 DOI: 10.1038/Ki.2013.227 |
0.304 |
|
| 2014 |
Trevisson E, Forzan M, Salviati L, Clementi M. Neurofibromatosis type 1 in two siblings due to maternal germline mosaicism. Clinical Genetics. 85: 386-9. PMID 23621909 DOI: 10.1111/cge.12177 |
0.336 |
|
| 2013 |
Morcaldi G, Clementi M, Lama G, Gabrielli O, Vannelli S, Virdis R, Vivarelli R, Boero S, Bonioli E. Evaluation of tibial osteopathy occurrence in neurofibromatosis type 1 Italian patients. American Journal of Medical Genetics. Part A. 161: 927-34. PMID 23463485 DOI: 10.1002/ajmg.a.35753 |
0.302 |
|
| 2013 |
Winterfeld U, Allignol A, Panchaud A, Rothuizen LE, Merlob P, Cuppers-Maarschalkerweerd B, Vial T, Stephens S, Clementi M, De Santis M, Pistelli A, Berlin M, Eleftheriou G, Maňáková E, Buclin T. Pregnancy outcome following maternal exposure to statins: a multicentre prospective study. Bjog : An International Journal of Obstetrics and Gynaecology. 120: 463-71. PMID 23194157 DOI: 10.1111/1471-0528.12066 |
0.351 |
|
| 2012 |
de Palma L, Boniver C, Cassina M, Toldo I, Nosadini M, Clementi M, Sartori S. Eating-induced epileptic spasms in a boy with MECP2 duplication syndrome: insights into pathogenesis of genetic epilepsies. Epileptic Disorders : International Epilepsy Journal With Videotape. 14: 414-7. PMID 23248047 DOI: 10.1684/epd.2012.0546 |
0.324 |
|
| 2012 |
Bar-Oz B, Weber-Schoendorfer C, Berlin M, Clementi M, Di Gianantonio E, de Vries L, De Santis M, Merlob P, Stahl B, Eleftheriou G, Maňáková E, HubiÄková-Heringová L, Youngster I, Berkovitch M. The outcomes of pregnancy in women exposed to the new macrolides in the first trimester: a prospective, multicentre, observational study. Drug Safety. 35: 589-98. PMID 22702640 DOI: 10.2165/11630920-000000000-00000 |
0.307 |
|
| 2012 |
Cassina M, Salviati L, Di Gianantonio E, Clementi M. Genetic susceptibility to teratogens: state of the art. Reproductive Toxicology (Elmsford, N.Y.). 34: 186-91. PMID 22659091 DOI: 10.1016/j.reprotox.2012.05.004 |
0.319 |
|
| 2012 |
Cassina M, Donà M, Di Gianantonio E, Clementi M. Pharmacologic treatment of hyperthyroidism during pregnancy. Birth Defects Research. Part a, Clinical and Molecular Teratology. 94: 612-9. PMID 22511519 DOI: 10.1002/bdra.23012 |
0.351 |
|
| 2012 |
Hoeltzenbein M, Elefant E, Vial T, Finkel-Pekarsky V, Stephens S, Clementi M, Allignol A, Weber-Schoendorfer C, Schaefer C. Teratogenicity of mycophenolate confirmed in a prospective study of the European Network of Teratology Information Services. American Journal of Medical Genetics. Part A. 158: 588-96. PMID 22319001 DOI: 10.1002/ajmg.a.35223 |
0.368 |
|
| 2012 |
Novelli A, Grati FR, Ballarati L, Bernardini L, Bizzoco D, Camurri L, Casalone R, Cardarelli L, Cavalli P, Ciccone R, Clementi M, Dalprà L, Gentile M, Gelli G, Grammatico P, et al. Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011. Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology. 39: 384-8. PMID 22262341 DOI: 10.1002/uog.11092 |
0.353 |
|
| 2012 |
Artuso R, Fallerini C, Dosa L, Scionti F, Clementi M, Garosi G, Massella L, Epistolato MC, Mancini R, Mari F, Longo I, Ariani F, Renieri A, Bruttini M. Advances in Alport syndrome diagnosis using next-generation sequencing. European Journal of Human Genetics : Ejhg. 20: 50-7. PMID 21897443 DOI: 10.1038/ejhg.2011.164 |
0.319 |
|
| 2011 |
Orioli IM, Amar E, Bakker MK, Bermejo-Sánchez E, Bianchi F, Canfield MA, Clementi M, Correa A, Csáky-Szunyogh M, Feldkamp ML, Landau D, Leoncini E, Li Z, Lowry RB, Mastroiacovo P, et al. Cyclopia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 157: 344-57. PMID 22006661 DOI: 10.1002/ajmg.c.30323 |
0.374 |
|
| 2011 |
Bermejo-Sánchez E, Cuevas L, Amar E, Bakker MK, Bianca S, Bianchi F, Canfield MA, Castilla EE, Clementi M, Cocchi G, Feldkamp ML, Landau D, Leoncini E, Li Z, Lowry RB, et al. Amelia: a multi-center descriptive epidemiologic study in a large dataset from the International Clearinghouse for Birth Defects Surveillance and Research, and overview of the literature. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 157: 288-304. PMID 22002956 DOI: 10.1002/ajmg.c.30319 |
0.357 |
|
| 2011 |
Botto LD, Feldkamp ML, Amar E, Carey JC, Castilla EE, Clementi M, Cocchi G, de Walle HE, Halliday J, Leoncini E, Li Z, Lowry RB, Marengo LK, MartÃnez-FrÃas ML, Merlob P, et al. Acardia: epidemiologic findings and literature review from the International Clearinghouse for Birth Defects Surveillance and Research. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 157: 262-73. PMID 22002952 DOI: 10.1002/ajmg.c.30318 |
0.38 |
|
| 2011 |
Feldkamp ML, Botto LD, Amar E, Bakker MK, Bermejo-Sánchez E, Bianca S, Canfield MA, Castilla EE, Clementi M, Csaky-Szunyogh M, Leoncini E, Li Z, Lowry RB, Mastroiacovo P, Merlob P, et al. Cloacal exstrophy: an epidemiologic study from the International Clearinghouse for Birth Defects Surveillance and Research. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 157: 333-43. PMID 22002951 DOI: 10.1002/ajmg.c.30317 |
0.371 |
|
| 2011 |
Siffel C, Correa A, Amar E, Bakker MK, Bermejo-Sánchez E, Bianca S, Castilla EE, Clementi M, Cocchi G, Csáky-Szunyogh M, Feldkamp ML, Landau D, Leoncini E, Li Z, Lowry RB, et al. Bladder exstrophy: an epidemiologic study from the International Clearinghouse for Birth Defects Surveillance and Research, and an overview of the literature. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 157: 321-32. PMID 22002949 DOI: 10.1002/ajmg.c.30316 |
0.353 |
|
| 2011 |
Orioli IM, Amar E, Arteaga-Vazquez J, Bakker MK, Bianca S, Botto LD, Clementi M, Correa A, Csaky-Szunyogh M, Leoncini E, Li Z, López-Camelo JS, Lowry RB, Marengo L, MartÃnez-FrÃas ML, et al. Sirenomelia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research, and literature review. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 157: 358-73. PMID 22002878 DOI: 10.1002/ajmg.c.30324 |
0.36 |
|
| 2011 |
Bermejo-Sánchez E, Cuevas L, Amar E, Bianca S, Bianchi F, Botto LD, Canfield MA, Castilla EE, Clementi M, Cocchi G, Landau D, Leoncini E, Li Z, Lowry RB, Mastroiacovo P, et al. Phocomelia: a worldwide descriptive epidemiologic study in a large series of cases from the International Clearinghouse for Birth Defects Surveillance and Research, and overview of the literature. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 157: 305-20. PMID 22002800 DOI: 10.1002/ajmg.c.30320 |
0.362 |
|
| 2011 |
Vecchi M, Cassina M, Casarin A, Rigon C, Drigo P, De Palma L, Clementi M. Infantile epilepsy associated with mosaic 2q24 duplication including SCN2A and SCN3A. Seizure. 20: 813-6. PMID 21893419 DOI: 10.1016/j.seizure.2011.07.008 |
0.338 |
|
| 2011 |
Micale L, Augello B, Fusco C, Selicorni A, Loviglio MN, Silengo MC, Reymond A, Gumiero B, Zucchetti F, D'Addetta EV, Belligni E, Calcagnì A, Digilio MC, Dallapiccola B, Faravelli F, ... ... Clementi M, et al. Mutation spectrum of MLL2 in a cohort of Kabuki syndrome patients. Orphanet Journal of Rare Diseases. 6: 38. PMID 21658225 DOI: 10.1186/1750-1172-6-38 |
0.355 |
|
| 2011 |
Diav-Citrin O, Shechtman S, Halberstadt Y, Finkel-Pekarsky V, Wajnberg R, Arnon J, Di Gianantonio E, Clementi M, Ornoy A. Pregnancy outcome after in utero exposure to angiotensin converting enzyme inhibitors or angiotensin receptor blockers. Reproductive Toxicology (Elmsford, N.Y.). 31: 540-5. PMID 21338666 DOI: 10.1016/j.reprotox.2011.02.008 |
0.323 |
|
| 2010 |
Clementi M, Di Gianantonio E, Cassina M, Leoncini E, Botto LD, Mastroiacovo P. Treatment of hyperthyroidism in pregnancy and birth defects. The Journal of Clinical Endocrinology and Metabolism. 95: E337-41. PMID 20668039 DOI: 10.1210/jc.2010-0652 |
0.329 |
|
| 2010 |
Cassina M, Di Gianantonio E, Toldo I, Battistella PA, Clementi M. Migraine therapy during pregnancy and lactation. Expert Opinion On Drug Safety. 9: 937-48. PMID 20662551 DOI: 10.1517/14740338.2010.505601 |
0.305 |
|
| 2010 |
Grati FR, Barlocco A, Grimi B, Milani S, Frascoli G, Di Meco AM, Liuti R, Trotta A, Chinetti S, Dulcetti F, Ruggeri AM, De Toffol S, Clementi M, Maggi F, Simoni G. Chromosome abnormalities investigated by non-invasive prenatal testing account for approximately 50% of fetal unbalances associated with relevant clinical phenotypes. American Journal of Medical Genetics. Part A. 152: 1434-42. PMID 20503318 DOI: 10.1002/ajmg.a.33370 |
0.336 |
|
| 2010 |
Cassina M, De Santis M, Cesari E, van Eijkeren M, Berkovitch M, Eleftheriou G, Raffagnato F, Di Gianantonio E, Clementi M. First trimester diclofenac exposure and pregnancy outcome. Reproductive Toxicology (Elmsford, N.Y.). 30: 401-4. PMID 20438830 DOI: 10.1016/j.reprotox.2010.04.010 |
0.339 |
|
| 2010 |
Losada I, Sartori L, Di Gianantonio E, Zen M, Clementi M, Doria A. Bisphosphonates in patients with autoimmune rheumatic diseases: Can they be used in women of childbearing age? Autoimmunity Reviews. 9: 547-52. PMID 20307690 DOI: 10.1016/j.autrev.2010.03.002 |
0.309 |
|
| 2009 |
Casarin A, Rusalen F, Doimo M, Trevisson E, Carraro S, Clementi M, Tenconi R, Baraldi E, Salviati L. X-linked brachytelephalangic chondrodysplasia punctata: a simple trait that is not so simple. American Journal of Medical Genetics. Part A. 149: 2464-8. PMID 19839041 DOI: 10.1002/ajmg.a.33039 |
0.355 |
|
| 2009 |
Cassina M, Fabris L, Okolicsanyi L, Gervasi MT, Memmo A, Tiboni GM, Di Gianantonio E, Clementi M. Therapy of inflammatory bowel diseases in pregnancy and lactation. Expert Opinion On Drug Safety. 8: 695-707. PMID 19832551 DOI: 10.1517/14740330903357463 |
0.306 |
|
| 2009 |
Corradi V, Gastaldon F, Virzì GM, de Cal M, Soni S, Chionh C, Cruz DN, Clementi M, Ronco C. Clinical pattern of adult polycystic kidney disease in a northeastern region of Italy. Clinical Nephrology. 72: 259-67. PMID 19825331 DOI: 10.5414/Cnp72259 |
0.331 |
|
| 2008 |
Diav-Citrin O, Shechtman S, Weinbaum D, Wajnberg R, Avgil M, Di Gianantonio E, Clementi M, Weber-Schoendorfer C, Schaefer C, Ornoy A. Paroxetine and fluoxetine in pregnancy: a prospective, multicentre, controlled, observational study. British Journal of Clinical Pharmacology. 66: 695-705. PMID 18754846 DOI: 10.1111/j.1365-2125.2008.03261.x |
0.337 |
|
| 2008 |
Schaefer C, Ornoy A, Clementi M, Meister R, Weber-Schoendorfer C. Using observational cohort data for studying drug effects on pregnancy outcome--methodological considerations. Reproductive Toxicology (Elmsford, N.Y.). 26: 36-41. PMID 18588969 DOI: 10.1016/j.reprotox.2008.05.064 |
0.324 |
|
| 2008 |
Weber-Schoendorfer C, Hannemann D, Meister R, Eléfant E, Cuppers-Maarschalkerweerd B, Arnon J, Vial T, Rodriguez-Pinilla E, Clementi M, Robert-Gnansia E, De Santis M, Malm H, Dolivo A, Schaefer C. The safety of calcium channel blockers during pregnancy: a prospective, multicenter, observational study. Reproductive Toxicology (Elmsford, N.Y.). 26: 24-30. PMID 18585452 DOI: 10.1016/j.reprotox.2008.05.065 |
0.304 |
|
| 2007 |
Goldstein LH, Dolinsky G, Greenberg R, Schaefer C, Cohen-Kerem R, Diav-Citrin O, Malm H, Reuvers-Lodewijks ME, Rost van Tonningen-van Driel MM, Arnon J, Ornoy A, Clementi M, Di Gianantonio E, Koren G, Braunstein R, et al. Pregnancy outcome of women exposed to azathioprine during pregnancy. Birth Defects Research. Part a, Clinical and Molecular Teratology. 79: 696-701. PMID 17847119 DOI: 10.1002/Bdra.20399 |
0.317 |
|
| 2007 |
Clementi M, Causin R, Marzocchi C, Mantovani A, Tenconi R. A study of the impact of agricultural pesticide use on the prevalence of birth defects in northeast Italy. Reproductive Toxicology (Elmsford, N.Y.). 24: 1-8. PMID 17561371 DOI: 10.1016/j.reprotox.2007.04.066 |
0.339 |
|
| 2006 |
Midrio P, Nogare CD, Di Gianantonio E, Clementi M. Are congenital anorectal malformations more frequent in newborns conceived with assisted reproductive techniques? Reproductive Toxicology (Elmsford, N.Y.). 22: 576-7. PMID 16815669 DOI: 10.1016/j.reprotox.2006.05.004 |
0.302 |
|
| 2006 |
Schaefer C, Hannemann D, Meister R, Eléfant E, Paulus W, Vial T, Reuvers M, Robert-Gnansia E, Arnon J, De Santis M, Clementi M, Rodriguez-Pinilla E, Dolivo A, Merlob P. Vitamin K antagonists and pregnancy outcome. A multi-centre prospective study. Thrombosis and Haemostasis. 95: 949-57. PMID 16732373 DOI: 10.1160/TH06-02-0108 |
0.306 |
|
| 2005 |
Botta A, Tacconelli A, Bagni I, Giardina E, Bonifazi E, Pietropolli A, Clementi M, Novelli G. Transmission ratio distortion in the spinal muscular atrophy locus: data from 314 prenatal tests. Neurology. 65: 1631-5. PMID 16301493 DOI: 10.1212/01.wnl.0000184506.61354.5b |
0.319 |
|
| 2005 |
Wiesel A, Queisser-Luft A, Clementi M, Bianca S, Stoll C. Prenatal detection of congenital renal malformations by fetal ultrasonographic examination: an analysis of 709,030 births in 12 European countries. European Journal of Medical Genetics. 48: 131-44. PMID 16053904 DOI: 10.1016/j.ejmg.2005.02.003 |
0.327 |
|
| 2005 |
De Santis M, Di Gianantonio E, Straface G, Cavaliere AF, Caruso A, Schiavon F, Berletti R, Clementi M. Ionizing radiations in pregnancy and teratogenesis: a review of literature. Reproductive Toxicology (Elmsford, N.Y.). 20: 323-9. PMID 15925481 DOI: 10.1016/j.reprotox.2005.04.004 |
0.314 |
|
| 2005 |
Bar-Oz B, Clementi M, Di Giantonio E, Greenberg R, Beer M, Merlob P, Arnon J, Ornoy A, Zimmerman DM, Berkovitch M. Metamizol (dipyrone, optalgin) in pregnancy, is it safe? A prospective comparative study. European Journal of Obstetrics, Gynecology, and Reproductive Biology. 119: 176-9. PMID 15808375 DOI: 10.1016/j.ejogrb.2004.07.004 |
0.339 |
|
| 2005 |
Diav-Citrin O, Shechtman S, Ornoy S, Arnon J, Schaefer C, Garbis H, Clementi M, Ornoy A. Safety of haloperidol and penfluridol in pregnancy: a multicenter, prospective, controlled study. The Journal of Clinical Psychiatry. 66: 317-22. PMID 15766297 DOI: 10.4088/Jcp.V66N0307 |
0.347 |
|
| 2005 |
Garbis H, Elefant E, Diav-Citrin O, Mastroiacovo P, Schaefer C, Vial T, Clementi M, Valti E, McElhatton P, Smorlesi C, Rodriguez EP, Robert-Gnansia E, Merlob P, Peiker G, Pexieder T, et al. Pregnancy outcome after exposure to ranitidine and other H2-blockers. A collaborative study of the European Network of Teratology Information Services. Reproductive Toxicology (Elmsford, N.Y.). 19: 453-8. PMID 15749258 DOI: 10.1016/j.reprotox.2004.09.002 |
0.33 |
|
| 2005 |
Diav-Citrin O, Arnon J, Shechtman S, Schaefer C, van Tonningen MR, Clementi M, De Santis M, Robert-Gnansia E, Valti E, Malm H, Ornoy A. The safety of proton pump inhibitors in pregnancy: a multicentre prospective controlled study. Alimentary Pharmacology & Therapeutics. 21: 269-75. PMID 15691301 DOI: 10.1111/j.1365-2036.2005.02306.x |
0.326 |
|
| 2004 |
Baena N, De Vigan C, Cariati E, Clementi M, Stoll C, CaballÃn MR, Guitart M. Turner syndrome: evaluation of prenatal diagnosis in 19 European registries. American Journal of Medical Genetics. Part A. 129: 16-20. PMID 15266609 DOI: 10.1002/ajmg.a.30092 |
0.376 |
|
| 2004 |
Venturin M, Guarnieri P, Natacci F, Stabile M, Tenconi R, Clementi M, Hernandez C, Thompson P, Upadhyaya M, Larizza L, Riva P. Mental retardation and cardiovascular malformations in NF1 microdeleted patients point to candidate genes in 17q11.2. Journal of Medical Genetics. 41: 35-41. PMID 14729829 DOI: 10.1136/Jmg.2003.014761 |
0.324 |
|
| 2003 |
Pramparo T, Gregato G, De Gregori M, Friso A, Clementi M, Ardenghi P, Rocchi M, Zuffardi O, Tenconi R. Reciprocal translocation associated with multiple exostoses in seven members of a three generation family and discovered through an infertile male. American Journal of Medical Genetics. Part A. 123: 79-83. PMID 14556251 DOI: 10.1002/ajmg.a.20498 |
0.306 |
|
| 2003 |
Stoll C, Clementi M. Prenatal diagnosis of dysmorphic syndromes by routine fetal ultrasound examination across Europe. Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology. 21: 543-51. PMID 12808670 DOI: 10.1002/uog.125 |
0.358 |
|
| 2003 |
Baena N, De Vigan C, Cariati E, Clementi M, Stoll C, Caballin MR, Guitart M, Haeusler M, Barisic I, Matejic R, Garne E, Vodovar V, Alembik Y, Dott B, Froster UG, et al. Prenatal detection of rare chromosomal autosomal abnormalities in Europe American Journal of Medical Genetics. 118: 319-327. PMID 12687662 DOI: 10.1002/Ajmg.A.10104 |
0.36 |
|
| 2002 |
Haeusler MCH, Berghold A, Stoll C, Barisic I, Clementi M, Gjergja-Matejic R, Garne E, De Vignan C, Vodovar V, Alembik Y, Dott B, Froster UG, Queisser-Luft A, Wiesel A, Tenconi R, et al. Prenatal ultrasonographic detection of gastrointestinal obstruction: Results from 18 European congenital anomaly registries Prenatal Diagnosis. 22: 616-623. PMID 12124699 DOI: 10.1002/pd.341 |
0.341 |
|
| 2002 |
Garne E, Haeusler M, Barišić I, Gjergja R, Stoll C, Clementi M. Congenital diaphragmatic hernia: evaluation of prenatal diagnosis in 20 European regions Ultrasound in Obstetrics & Gynecology. 19: 329-333. PMID 11952959 DOI: 10.1046/J.1469-0705.2002.00635.X |
0.374 |
|
| 2001 |
Barisic I, Clementi M, Häusler M, Gjergja R, Kern J, Stoll C. Evaluation of prenatal ultrasound diagnosis of fetal abdominal wall defects by 19 European registries. Ultrasound in Obstetrics & Gynecology. 18: 309-316. PMID 11778988 DOI: 10.1046/J.0960-7692.2001.00534.X |
0.374 |
|
| 2001 |
Vigan CD, Baena N, Cariati E, Clementi M, Stoll C. Contribution of ultrasonographic examination to the prenatal detection of chromosomal abnormalities in 19 centres across Europe. Annales De Genetique. 44: 209-217. PMID 11755107 DOI: 10.1016/S0003-3995(01)01091-7 |
0.363 |
|
| 2001 |
Garne E, Stoll C, Clementi M. Evaluation of prenatal diagnosis of congenital heart diseases by ultrasound: experience from 20 European registries Ultrasound in Obstetrics & Gynecology. 17: 386-391. PMID 11380961 DOI: 10.1046/J.1469-0705.2001.00385.X |
0.324 |
|
| 2001 |
Stoll C, Garne E, Clementi M. Evaluation of prenatal diagnosis of associated congenital heart diseases by fetal ultrasonographic examination in Europe. Prenatal Diagnosis. 21: 243-252. PMID 11288111 DOI: 10.1002/Pd.34 |
0.374 |
|
| 2001 |
Bassi MT, Bergen AA, Bitoun P, Charles SJ, Clementi M, Gosselin R, Hurst J, Lewis RA, Lorenz B, Meitinger T, Messiaen L, Ramesar RS, Ballabio A, Schiaffino MV. Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North America. Human Genetics. 108: 51-4. PMID 11214907 DOI: 10.1007/S004390000440 |
0.318 |
|
| 2001 |
Stoll C, Tenconi R, Clementi M, Haeusler M, Barisic I, Matejic R, Garne E, De Vigan C, Vodovar V, Alembik Y, Dott B, Froster UG, Queisser-Luft A, Wiesel A, Benedicenti F, et al. Detection of congenital anomalies by fetal ultrasonographic examination across Europe Community Genetics. 4: 225-232. DOI: 10.1159/000064197 |
0.359 |
|
| 2000 |
Boyd PA, Wellesley DG, De Walle HEK, Tenconi R, Garcia-Minaur S, Zandwijken GRJ, Stoll C, Clementi M. Evaluation of the prenatal diagnosis of neural tube defects by fetal ultrasonographic examination in different centres across Europe Journal of Medical Screening. 7: 169-174. PMID 11202581 DOI: 10.1136/jms.7.4.169 |
0.372 |
|
| 2000 |
Clementi M, Tenconi R, Bianchi F, Stoll C. Evaluation of prenatal diagnosis of cleft lip with or without cleft palate and cleft palate by ultrasound: experience from 20 European registries Prenatal Diagnosis. 20: 870-875. PMID 11113886 DOI: 10.1002/1097-0223(200011)20:11<870::Aid-Pd940>3.0.Co;2-J |
0.381 |
|
| 2000 |
Stoll C, Wiesel A, Queisserluft A, Froster U, Bianca S, Clementi M. Evaluation of the prenatal diagnosis of limb reduction deficiencies Prenatal Diagnosis. 20: 811-818. PMID 11038459 DOI: 10.1002/1097-0223(200010)20:10<811::Aid-Pd927>3.0.Co;2-J |
0.39 |
|
| 2000 |
Riva P, Corrado L, Natacci F, Castorina P, Wu BL, Schneider GH, Clementi M, Tenconi R, Korf BR, Larizza L. NF1 Microdeletion Syndrome: Refined FISH Characterization of Sporadic and Familial Deletions with Locus-Specific Probes American Journal of Human Genetics. 66: 100-109. PMID 10631140 DOI: 10.1086/302709 |
0.324 |
|
| 1999 |
Correa CL, Brems H, Lázaro C, Estivill X, Clementi M, Mason S, Rutkowski JL, Marynen P, Legius E. Molecular studies in 20 submicroscopic neurofibromatosis type 1 gene deletions. Human Mutation. 14: 387-393. PMID 10533064 DOI: 10.1002/(Sici)1098-1004(199911)14:5<387::Aid-Humu4>3.0.Co;2-4 |
0.323 |
|
| 1999 |
Clementi M, Gianantonio ED, Pelo E, Mammi I, Basile RT, Tenconi R. Methimazole embryopathy: delineation of the phenotype. American Journal of Medical Genetics. 83: 43-46. PMID 10076883 DOI: 10.1002/(Sici)1096-8628(19990305)83:1<43::Aid-Ajmg8>3.0.Co;2-C |
0.368 |
|
| 1999 |
Mastroiacovo P, Mazzone T, Addis A, Elephant E, Carlier P, Vial T, Garbis H, Robert E, Bonati M, Ornoy A, Finardi A, Schaffer C, Caramelli L, Rodríguez‐Pinilla E, Clementi M. High vitamin A intake in early pregnancy and major malformations: a multicenter prospective controlled study. Teratology. 59: 7-11. PMID 9988877 DOI: 10.1002/(Sici)1096-9926(199901)59:1<7::Aid-Tera4>3.0.Co;2-6 |
0.306 |
|
| 1998 |
Mammi I, Giorgio PD, Clementi M, Tenconi R. Cardiovascular Anomaly In Rieger Syndrome : Heterogeneity Or Contiguity? Acta Ophthalmologica Scandinavica. 76: 509-512. PMID 9716345 DOI: 10.1034/J.1600-0420.1998.760424.X |
0.314 |
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| 1998 |
Superti-Furga A, Tenconi R, Clementi M, Eich G, Steinmann B, Boltshauser E, Giedion A. Schwartz-Jampel syndrome type 2 and Stüve-Wiedemann syndrome: A case for “Lumping” American Journal of Medical Genetics. 78: 150-154. PMID 9674906 DOI: 10.1002/(Sici)1096-8628(19980630)78:2<150::Aid-Ajmg10>3.0.Co;2-M |
0.334 |
|
| 1997 |
Clementi M, Tenconi R, Forabosco P, Calzolari E, Milan M. Inheritance of cleft palate in Italy. Evidence for a major autosomal recessive locus Human Genetics. 100: 204-209. PMID 9254850 DOI: 10.1007/s004390050491 |
0.362 |
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| 1997 |
Clementi M, Mammi I, Tenconi R. Family with branchial arch anomalies, hearing loss, ear and commissural lip pits, and rib anomalies. A new autosomal recessive condition : Branchio-oto-costal syndrome? American Journal of Medical Genetics. 68: 91-93. PMID 8986284 DOI: 10.1002/(Sici)1096-8628(19970110)68:1<91::Aid-Ajmg18>3.0.Co;2-J |
0.332 |
|
| 1996 |
Mammi I, Iles DE, Smeets D, Clementi M, Tenconi R. Anesthesiologic problems in Williams syndrome: the CACNL2A locus is not involved Human Genetics. 98: 317-320. PMID 8707301 DOI: 10.1007/S004390050214 |
0.311 |
|
| 1995 |
Clementi M, Tenconi R, Collins A, Calzolari E, Milan M. Complex segregation analysis in a sample of consecutive newborns with cleft lip with or without cleft palate in Italy Human Heredity. 45: 157-164. PMID 7615301 DOI: 10.1159/000154277 |
0.311 |
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| 1994 |
Milan M, Astolfi G, Volpato S, Garani GP, Clementi M, Tenconi R, Boni S, Calzolari E. 766 cases of oral cleft in Italy. Data from Emilia Romagna (IMER) and northeast Italy (NEI) registers. European Journal of Epidemiology. 10: 317-324. PMID 7859843 DOI: 10.1007/Bf01719356 |
0.334 |
|
| 1994 |
Spagnolo A, Bianchi F, Calabro A, Calzolari E, Clementi M, Mastroiacovo P, Meli P, Petrelli G, Tenconi R. Anophthalmia and benomyl in Italy: a multicenter study based on 940,615 newborns Reproductive Toxicology. 8: 397-403. PMID 7841658 DOI: 10.1016/0890-6238(94)90079-5 |
0.341 |
|
| 1993 |
Calzolari E, Volpato S, Bianchi F, Cianciulli D, Tenconi R, Clementi M, Calabro A, Lungarotti S, Mastroiacovo PP, Botto L, Spagnolo A, Milan M. Omphalocele and gastroschisis: a collaborative study of five Italian congenital malformation registries. Teratology. 47: 47-55. PMID 8475457 DOI: 10.1002/Tera.1420470109 |
0.341 |
|
| 1993 |
Minelli A, Floridia G, Rossi E, Clementi M, Tenconi R, Camurri L, Bernardi F, Hoeller H, Previde Re C, Maraschio P. D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p). Human Genetics. 92: 391-6. PMID 7901142 DOI: 10.1007/Bf01247342 |
0.316 |
|
| 1992 |
Clementi M, Turolla L, Mammi I, Tenconi R. Clinical anophthalmia: an epidemiological study in northeast Italy based on 368,256 consecutive births. Teratology. 46: 551-553. PMID 1290155 DOI: 10.1002/Tera.1420460604 |
0.368 |
|
| 1990 |
Turolla L, Clementi M, Tenconi R. How wide is the clinical spectrum of the acrocallosal syndrome? Report of a mild case. Journal of Medical Genetics. 27: 516-518. PMID 2103730 DOI: 10.1136/Jmg.27.8.516 |
0.301 |
|
| 1984 |
Audino G, Tenconi R, Clementi M, Saia OS, Cordioli GP. Popliteal pterygium syndrome presenting with orofacial abnormalities. Report of a family. Journal of Maxillofacial Surgery. 12: 174-7. PMID 6590717 DOI: 10.1016/S0301-0503(84)80240-4 |
0.342 |
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