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

Year Number of Results
1948 1
1977 2
1979 1
1980 1
1981 1
1982 1
1985 1
1987 2
1988 3
1990 1
1991 1
1992 3
1994 1
1996 4
1997 1
1998 1
1999 1
2000 4
2001 4
2002 1
2003 2
2004 2
2005 1
2006 4
2007 8
2008 3
2009 9
2010 10
2011 14
2012 10
2013 10
2014 14
2015 14
2016 24
2017 17
2018 18
2019 15
2020 21
2021 30
2022 23
2023 30
2024 14

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265 results

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Page 1
Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG).
Gregg AR, Aarabi M, Klugman S, Leach NT, Bashford MT, Goldwaser T, Chen E, Sparks TN, Reddi HV, Rajkovic A, Dungan JS; ACMG Professional Practice and Guidelines Committee. Gregg AR, et al. Among authors: sparks tn. Genet Med. 2021 Oct;23(10):1793-1806. doi: 10.1038/s41436-021-01203-z. Epub 2021 Jul 20. Genet Med. 2021. PMID: 34285390 Free PMC article.
Hypospadias.
Society for Maternal-Fetal Medicine (SMFM); Sparks TN. Society for Maternal-Fetal Medicine (SMFM), et al. Among authors: sparks tn. Am J Obstet Gynecol. 2021 Nov;225(5):B18-B20. doi: 10.1016/j.ajog.2021.06.045. Epub 2021 Sep 8. Am J Obstet Gynecol. 2021. PMID: 34507799 No abstract available.
Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis.
Sparks TN, Lianoglou BR, Adami RR, Pluym ID, Holliman K, Duffy J, Downum SL, Patel S, Faubel A, Boe NM, Field NT, Murphy A, Laurent LC, Jolley J, Uy C, Slavotinek AM, Devine P, Hodoglugil U, Van Ziffle J, Sanders SJ, MacKenzie TC, Norton ME; University of California Fetal–Maternal Consortium; University of California, San Francisco Center for Maternal–Fetal Precision Medicine. Sparks TN, et al. N Engl J Med. 2020 Oct 29;383(18):1746-1756. doi: 10.1056/NEJMoa2023643. Epub 2020 Oct 7. N Engl J Med. 2020. PMID: 33027564 Free PMC article.
Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series.
Brar BK, Thompson MG, Vora NL, Gilmore K, Blakemore K, Miller KA, Giordano J, Dufke A, Wong B, Stover S, Lianoglou B, Van den Veyver I, Dempsey E, Rosner M, Chong K, Chitayat D, Sparks TN, Norton ME, Wapner R, Baranano K, Jelin AC; Fetal Sequencing Consortium. Brar BK, et al. Among authors: sparks tn. Prenat Diagn. 2022 Dec;42(13):1686-1693. doi: 10.1002/pd.6269. Epub 2022 Nov 28. Prenat Diagn. 2022. PMID: 36403095 Free PMC article. Review.
Cell-type specialization is encoded by specific chromatin topologies.
Winick-Ng W, Kukalev A, Harabula I, Zea-Redondo L, Szabó D, Meijer M, Serebreni L, Zhang Y, Bianco S, Chiariello AM, Irastorza-Azcarate I, Thieme CJ, Sparks TM, Carvalho S, Fiorillo L, Musella F, Irani E, Torlai Triglia E, Kolodziejczyk AA, Abentung A, Apostolova G, Paul EJ, Franke V, Kempfer R, Akalin A, Teichmann SA, Dechant G, Ungless MA, Nicodemi M, Welch L, Castelo-Branco G, Pombo A. Winick-Ng W, et al. Among authors: sparks tm. Nature. 2021 Nov;599(7886):684-691. doi: 10.1038/s41586-021-04081-2. Epub 2021 Nov 17. Nature. 2021. PMID: 34789882 Free PMC article.
Prenatal phenotype of 47, XXY (Klinefelter syndrome).
Swanson K, Bishop JC, Al-Kouatly HB, Makhamreh M, Felton T, Vora NL, Sparks TN, Jelin AC. Swanson K, et al. Among authors: sparks tn. Prenat Diagn. 2023 Feb;43(2):207-212. doi: 10.1002/pd.6071. Epub 2021 Dec 7. Prenat Diagn. 2023. PMID: 34874073 Free PMC article. Review.
265 results