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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1990 1
1993 3
1994 3
1995 5
1996 5
1997 1
1998 3
1999 2
2000 2
2001 3
2002 2
2003 1
2004 5
2005 3
2006 2
2007 6
2008 11
2009 22
2010 9
2011 17
2012 8
2013 10
2014 14
2015 21
2016 6
2017 10
2018 11
2019 24
2020 22
2021 13
2022 16
2023 15
2024 3

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241 results

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Page 1
Health Supervision for Children and Adolescents With Down Syndrome.
Bull MJ, Trotter T, Santoro SL, Christensen C, Grout RW; COUNCIL ON GENETICS; Burke LW, Berry SA, Geleske TA, Holm I, Hopkin RJ, Introne WJ, Lyons MJ, Monteil DC, Scheuerle A, Stoler JM, Vergano SA, Chen E, Hamid R, Downs SM, Grout RW, Cunniff C, Parisi MA, Ralston SJ, Scott JA, Shapira SK, Spire P. Bull MJ, et al. Among authors: scheuerle a. Pediatrics. 2022 May 1;149(5):e2022057010. doi: 10.1542/peds.2022-057010. Pediatrics. 2022. PMID: 35490285 No abstract available.
Incontinentia Pigmenti.
Scheuerle AE, Ursini MV. Scheuerle AE, et al. 1999 Jun 8 [updated 2017 Dec 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 1999 Jun 8 [updated 2017 Dec 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301645 Free Books & Documents. Review.
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms.
Kaur M, Blair J, Devkota B, Fortunato S, Clark D, Lawrence A, Kim J, Do W, Semeo B, Katz O, Mehta D, Yamamoto N, Schindler E, Al Rawi Z, Wallace N, Wilde JJ, McCallum J, Liu J, Xu D, Jackson M, Rentas S, Tayoun AA, Zhe Z, Abdul-Rahman O, Allen B, Angula MA, Anyane-Yeboa K, Argente J, Arn PH, Armstrong L, Basel-Salmon L, Baynam G, Bird LM, Bruegger D, Ch'ng GS, Chitayat D, Clark R, Cox GF, Dave U, DeBaere E, Field M, Graham JM Jr, Gripp KW, Greenstein R, Gupta N, Heidenreich R, Hoffman J, Hopkin RJ, Jones KL, Jones MC, Kariminejad A, Kogan J, Lace B, Leroy J, Lynch SA, McDonald M, Meagher K, Mendelsohn N, Micule I, Moeschler J, Nampoothiri S, Ohashi K, Powell CM, Ramanathan S, Raskin S, Roeder E, Rio M, Rope AF, Sangha K, Scheuerle AE, Schneider A, Shalev S, Siu V, Smith R, Stevens C, Tkemaladze T, Toimie J, Toriello H, Turner A, Wheeler PG, White SM, Young T, Loomes KM, Pipan M, Harrington AT, Zackai E, Rajagopalan R, Conlin L, Deardorff MA, McEldrew D, Pie J, Ramos F, Musio A, Kline AD, Izumi K, Raible SE, Krantz ID. Kaur M, et al. Among authors: scheuerle ae. Am J Med Genet A. 2023 Aug;191(8):2113-2131. doi: 10.1002/ajmg.a.63247. Epub 2023 Jun 28. Am J Med Genet A. 2023. PMID: 37377026
Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype.
Hiatt SM, Trajkova S, Sebastiano MR, Partridge EC, Abidi FE, Anderson A, Ansar M, Antonarakis SE, Azadi A, Bachmann-Gagescu R, Bartuli A, Benech C, Berkowitz JL, Betti MJ, Brusco A, Cannon A, Caron G, Chen Y, Cochran ME, Coleman TF, Crenshaw MM, Cuisset L, Curry CJ, Darvish H, Demirdas S, Descartes M, Douglas J, Dyment DA, Elloumi HZ, Ermondi G, Faoucher M, Farrow EG, Felker SA, Fisher H, Hurst ACE, Joset P, Kelly MA, Kmoch S, Leadem BR, Lyons MJ, Macchiaiolo M, Magner M, Mandrile G, Mattioli F, McEown M, Meadows SK, Medne L, Meeks NJL, Montgomery S, Napier MP, Natowicz M, Newberry KM, Niceta M, Noskova L, Nowak CB, Noyes AG, Osmond M, Prijoles EJ, Pugh J, Pullano V, Quélin C, Rahimi-Aliabadi S, Rauch A, Redon S, Reymond A, Schwager CR, Sellars EA, Scheuerle AE, Shukarova-Angelovska E, Skraban C, Stolerman E, Sullivan BR, Tartaglia M, Thiffault I, Uguen K, Umaña LA, van Bever Y, van der Crabben SN, van Slegtenhorst MA, Waisfisz Q, Washington C, Rodan LH, Myers RM, Cooper GM. Hiatt SM, et al. Among authors: scheuerle ae. Am J Hum Genet. 2023 Feb 2;110(2):215-227. doi: 10.1016/j.ajhg.2022.12.007. Epub 2022 Dec 30. Am J Hum Genet. 2023. PMID: 36586412 Free PMC article.
The childless man.
Scheuerle AE, Picconi JL, Neidich J, Panny S, Plecher BA, Randolph LM, Trapane P, Trotter TL. Scheuerle AE, et al. Am J Med Genet A. 2014 Feb;164A(2):561. doi: 10.1002/ajmg.a.36290. Epub 2013 Dec 5. Am J Med Genet A. 2014. PMID: 24311465 No abstract available.
Medicine's questions.
Scheuerle A. Scheuerle A. J Craniofac Surg. 2010 Sep;21(5):1335. doi: 10.1097/SCS.0b013e3181ecc573. J Craniofac Surg. 2010. PMID: 20856018 No abstract available.
Reading genetic-speak.
Scheuerle A. Scheuerle A. J Craniofac Surg. 2010 Sep;21(5):1319-20. doi: 10.1097/SCS.0b013e3181ecc584. J Craniofac Surg. 2010. PMID: 20856014 No abstract available.
Asymmetric faces: Symbolic, spiritual, and representative.
Scheuerle AE, Firth RM. Scheuerle AE, et al. Am J Med Genet C Semin Med Genet. 2021 Jun;187(2):278-282. doi: 10.1002/ajmg.c.31901. Epub 2021 May 13. Am J Med Genet C Semin Med Genet. 2021. PMID: 33982860
Incontinentia pigmenti in adults.
Scheuerle AE. Scheuerle AE. Am J Med Genet A. 2019 Aug;179(8):1415-1419. doi: 10.1002/ajmg.a.61205. Epub 2019 May 22. Am J Med Genet A. 2019. PMID: 31119873
Bcl-XL but Not Bcl-2 Is a Potential Target in Medulloblastoma Therapy.
Westhoff MA, Schuler-Ortoli M, Zerrinius D, Hadzalic A, Schuster A, Strobel H, Scheuerle A, Wong T, Wirtz CR, Debatin KM, Peraud A. Westhoff MA, et al. Among authors: scheuerle a. Pharmaceuticals (Basel). 2022 Jan 14;15(1):91. doi: 10.3390/ph15010091. Pharmaceuticals (Basel). 2022. PMID: 35056150 Free PMC article.
241 results