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Page 1
SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females.
Radio FC, Pang K, Ciolfi A, Levy MA, Hernández-García A, Pedace L, Pantaleoni F, Liu Z, de Boer E, Jackson A, Bruselles A, McConkey H, Stellacci E, Lo Cicero S, Motta M, Carrozzo R, Dentici ML, McWalter K, Desai M, Monaghan KG, Telegrafi A, Philippe C, Vitobello A, Au M, Grand K, Sanchez-Lara PA, Baez J, Lindstrom K, Kulch P, Sebastian J, Madan-Khetarpal S, Roadhouse C, MacKenzie JJ, Monteleone B, Saunders CJ, Jean Cuevas JK, Cross L, Zhou D, Hartley T, Sawyer SL, Monteiro FP, Secches TV, Kok F, Schultz-Rogers LE, Macke EL, Morava E, Klee EW, Kemppainen J, Iascone M, Selicorni A, Tenconi R, Amor DJ, Pais L, Gallacher L, Turnpenny PD, Stals K, Ellard S, Cabet S, Lesca G, Pascal J, Steindl K, Ravid S, Weiss K, Castle AMR, Carter MT, Kalsner L, de Vries BBA, van Bon BW, Wevers MR, Pfundt R, Stegmann APA, Kerr B, Kingston HM, Chandler KE, Sheehan W, Elias AF, Shinde DN, Towne MC, Robin NH, Goodloe D, Vanderver A, Sherbini O, Bluske K, Hagelstrom RT, Zanus C, Faletra F, Musante L, Kurtz-Nelson EC, Earl RK, Anderlid BM, Morin G, van Slegtenhorst M, Diderich KEM, Brooks AS, Gribnau J, Boers RG, Finestra TR, Carter LB, Rauch A, Gasparini P, Boycott KM, Barakat TS, Graham JM Jr, Fai… See abstract for full author list ➔ Radio FC, et al. Among authors: monteleone b. Am J Hum Genet. 2021 Mar 4;108(3):502-516. doi: 10.1016/j.ajhg.2021.01.015. Epub 2021 Feb 16. Am J Hum Genet. 2021. PMID: 33596411 Free PMC article.
DNA methylation episignature for Witteveen-Kolk syndrome due to SIN3A haploinsufficiency.
Coenen-van der Spek J, Relator R, Kerkhof J, McConkey H, Levy MA, Tedder ML, Louie RJ, Fletcher RS, Moore HW, Childers A, Farrelly ER, Champaigne NL, Lyons MJ, Everman DB, Rogers RC, Skinner SA, Renck A, Matalon DR, Dills SK, Monteleone B, Demirdas S, Dingemans AJM, Donker Kaat L, Kolk SM, Pfundt R, Rump P, Sadikovic B, Kleefstra T, Butler KM. Coenen-van der Spek J, et al. Among authors: monteleone b. Genet Med. 2023 Jan;25(1):63-75. doi: 10.1016/j.gim.2022.10.004. Epub 2022 Nov 18. Genet Med. 2023. PMID: 36399132 Free article.
Mafic slab melt contributions to Proterozoic massif-type anorthosites.
Keller DS, Lee CA, Peck WH, Monteleone BD, Martin C, Vervoort JD, Bolge L. Keller DS, et al. Among authors: monteleone bd. Sci Adv. 2024 Aug 16;10(33):eadn3976. doi: 10.1126/sciadv.adn3976. Epub 2024 Aug 14. Sci Adv. 2024. PMID: 39141730 Free PMC article.
TRIM71 mutations cause a neurodevelopmental syndrome featuring ventriculomegaly and hydrocephalus.
Duy PQ, Jux B, Zhao S, Mekbib KY, Dennis E, Dong W, Nelson-Williams C, Mehta NH, Shohfi JP, Juusola J, Allington G, Smith H, Marlin S, Belhous K, Monteleone B, Schaefer GB, Pisarska MD, Vásquez J, Estrada-Veras JI, Keren B, Mignot C, Flore LA, Palafoll IV, Alper SL, Lifton RP, Haider S, Moreno-De-Luca A, Jin SC, Kolanus W, Kahle KT. Duy PQ, et al. Among authors: monteleone b. Brain. 2024 Jun 4:awae175. doi: 10.1093/brain/awae175. Online ahead of print. Brain. 2024. PMID: 38833623
Oceanic intraplate explosive eruptions fed directly from the mantle.
DeVitre CL, Gazel E, Ramalho RS, Venugopal S, Steele-MacInnis M, Hua J, Allison CM, Moore LR, Carracedo JC, Monteleone B. DeVitre CL, et al. Among authors: monteleone b. Proc Natl Acad Sci U S A. 2023 Aug 15;120(33):e2302093120. doi: 10.1073/pnas.2302093120. Epub 2023 Aug 7. Proc Natl Acad Sci U S A. 2023. PMID: 37549259 Free PMC article.
ChatGPT: a pioneering approach to complex prenatal differential diagnosis.
Suhag A, Kidd J, McGath M, Rajesh R, Gelfinbein J, Cacace N, Monteleone B, Chavez MR. Suhag A, et al. Among authors: monteleone b. Am J Obstet Gynecol MFM. 2023 Aug;5(8):101029. doi: 10.1016/j.ajogmf.2023.101029. Epub 2023 May 29. Am J Obstet Gynecol MFM. 2023. PMID: 37257586
27 results