| Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 RE Amir, IB Van den Veyver, M Wan, CQ Tran, U Francke, HY Zoghbi Nature genetics 23 (2), 185-188, 1999 | 5873 | 1999 |
| A metagenomic approach to characterization of the vaginal microbiome signature in pregnancy K Aagaard, K Riehle, J Ma, N Segata, TA Mistretta, C Coarfa, S Raza, ... PloS one 7 (6), e36466, 2012 | 859 | 2012 |
| Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes RE Amir, IB Van Den Veyver, R Schultz, DM Malicki, CQ Tran, EJ Dahle, ... Annals of neurology 47 (5), 670-679, 2000 | 422 | 2000 |
| Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasia X Wang, V Reid Sutton, J Omar Peraza-Llanes, Z Yu, R Rosetta, YC Kou, ... Nature genetics 39 (7), 836-838, 2007 | 292 | 2007 |
| Genetic effects of methylation diets IB Van den Veyver Annual review of nutrition 22 (1), 255-282, 2002 | 285 | 2002 |
| Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases IB Van den Veyver, A Patel, CA Shaw, AN Pursley, SHL Kang, ... Prenatal Diagnosis: Published in Affiliation With the International Society …, 2009 | 253 | 2009 |
| RETRACTED: A Mutant Form of MeCP2 Protein Associated with Human Rett Syndrome Cannot Be Displaced from Methylated DNA by Notch in Xenopus Embryos I Stancheva, AL Collins, IB Van den Veyver, H Zoghbi, RR Meehan Molecular cell 12 (2), 425-435, 2003 | 208 | 2003 |
| Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization T Sahoo, SW Cheung, P Ward, S Darilek, A Patel, D Del Gaudio, ... Genetics in Medicine 8 (11), 719-727, 2006 | 207 | 2006 |
| Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA J Zhang, J Li, JB Saucier, Y Feng, Y Jiang, J Sinson, AK McCombs, ... Nature medicine 25 (3), 439-447, 2019 | 196 | 2019 |
| Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory AK Petersen, SW Cheung, JL Smith, W Bi, PA Ward, S Peacock, ... American journal of obstetrics and gynecology 217 (6), 691. e1-691. e6, 2017 | 187 | 2017 |
| Genetic mapping of a maternal locus responsible for familial hydatidiform moles YB Moglabey, R Kircheisen, M Seoud, N El Mogharbel, I Van den Veyver, ... Human molecular genetics 8 (4), 667-667, 1999 | 169 | 1999 |
| Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with> 1000 cases and review of the literature A Breman, AN Pursley, P Hixson, W Bi, P Ward, CA Bacino, C Shaw, ... Prenatal diagnosis 32 (4), 351-361, 2012 | 150 | 2012 |
| A recurrent intragenic genomic duplication, other novel mutations in NLRP7 and imprinting defects in recurrent biparental hydatidiform moles YC Kou, L Shao, HH Peng, R Rosetta, D Del Gaudio, AF Wagner, ... MHR: Basic science of reproductive medicine 14 (1), 33-40, 2007 | 146 | 2007 |
| Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder EA Normand, A Braxton, S Nassef, PA Ward, F Vetrini, W He, V Patel, ... Genome medicine 10, 1-14, 2018 | 138 | 2018 |
| Prospective trial on obstructive sleep apnea in pregnancy and fetal heart rate monitoring SA Olivarez, B Maheshwari, M McCarthy, N Zacharias, I van den Veyver, ... American journal of obstetrics and gynecology 202 (6), 552. e1-552. e7, 2010 | 134 | 2010 |
| Skewed X inactivation in X-linked disorders IB Van den Veyver Seminars in reproductive medicine 19 (02), 183-192, 2001 | 133 | 2001 |
| Methyl-CpG-binding protein 2 mutations in Rett syndrome IB Van den Veyver, HY Zoghbi Current opinion in genetics & development 10 (3), 275-279, 2000 | 128 | 2000 |
| Preimplantation single cell analyses of dystrophin gene deletions using whole genome amplification K Kristjansson, SS Chong, IB Van den Veyver, S Subramanian, ... Nature genetics 6 (1), 19-23, 1994 | 128 | 1994 |
| Evidence for feasibility of fetal trophoblastic cell‐based noninvasive prenatal testing AM Breman, JC Chow, L U'Ren, EA Normand, S Qdaisat, L Zhao, ... Prenatal diagnosis 36 (11), 1009-1019, 2016 | 104 | 2016 |
| Biparental hydatidiform moles: a maternal effect mutation affecting imprinting in the offspring IB Van den Veyver, TK Al-Hussaini Human reproduction update 12 (3), 233-242, 2006 | 103 | 2006 |
