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

Year Number of Results
1962 1
1965 1
1966 2
1969 1
1971 1
1972 1
1973 3
1974 2
1975 1
1976 1
1977 1
1978 2
1981 2
1982 3
1983 2
1984 5
1985 2
1986 1
1987 2
1988 3
1989 3
1990 5
1991 7
1992 2
1993 4
1994 7
1995 10
1996 7
1997 4
1998 6
1999 7
2000 7
2001 9
2002 7
2003 11
2004 7
2005 9
2006 8
2007 9
2008 12
2009 21
2010 20
2011 16
2012 18
2013 12
2014 16
2015 13
2016 22
2017 19
2018 25
2019 15
2020 21
2021 16
2022 14
2023 17
2024 3

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415 results

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Page 1
Higher-Order Inter-chromosomal Hubs Shape 3D Genome Organization in the Nucleus.
Quinodoz SA, Ollikainen N, Tabak B, Palla A, Schmidt JM, Detmar E, Lai MM, Shishkin AA, Bhat P, Takei Y, Trinh V, Aznauryan E, Russell P, Cheng C, Jovanovic M, Chow A, Cai L, McDonel P, Garber M, Guttman M. Quinodoz SA, et al. Among authors: schmidt jm. Cell. 2018 Jul 26;174(3):744-757.e24. doi: 10.1016/j.cell.2018.05.024. Epub 2018 Jun 7. Cell. 2018. PMID: 29887377 Free PMC article.
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.
Braun DA, Rao J, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, Boyer O, Revy P, Jobst-Schwan T, Schmidt JM, Lawson JA, Schanze D, Ashraf S, Ullmann JFP, Hoogstraten CA, Boddaert N, Collinet B, Martin G, Liger D, Lovric S, Furlano M, Guerrera IC, Sanchez-Ferras O, Hu JF, Boschat AC, Sanquer S, Menten B, Vergult S, De Rocker N, Airik M, Hermle T, Shril S, Widmeier E, Gee HY, Choi WI, Sadowski CE, Pabst WL, Warejko JK, Daga A, Basta T, Matejas V, Scharmann K, Kienast SD, Behnam B, Beeson B, Begtrup A, Bruce M, Ch'ng GS, Lin SP, Chang JH, Chen CH, Cho MT, Gaffney PM, Gipson PE, Hsu CH, Kari JA, Ke YY, Kiraly-Borri C, Lai WM, Lemyre E, Littlejohn RO, Masri A, Moghtaderi M, Nakamura K, Ozaltin F, Praet M, Prasad C, Prytula A, Roeder ER, Rump P, Schnur RE, Shiihara T, Sinha MD, Soliman NA, Soulami K, Sweetser DA, Tsai WH, Tsai JD, Topaloglu R, Vester U, Viskochil DH, Vatanavicharn N, Waxler JL, Wierenga KJ, Wolf MTF, Wong SN, Leidel SA, Truglio G, Dedon PC, Poduri A, Mane S, Lifton RP, Bouchard M, Kannu P, Chitayat D, Magen D, Callewaert B, van Tilbeurgh H, Zenker M, Antignac C, Hildebrandt F. Braun DA, et al. Among authors: schmidt jm. Nat Genet. 2017 Oct;49(10):1529-1538. doi: 10.1038/ng.3933. Epub 2017 Aug 14. Nat Genet. 2017. PMID: 28805828 Free PMC article.
Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.
Warejko JK, Tan W, Daga A, Schapiro D, Lawson JA, Shril S, Lovric S, Ashraf S, Rao J, Hermle T, Jobst-Schwan T, Widmeier E, Majmundar AJ, Schneider R, Gee HY, Schmidt JM, Vivante A, van der Ven AT, Ityel H, Chen J, Sadowski CE, Kohl S, Pabst WL, Nakayama M, Somers MJG, Rodig NM, Daouk G, Baum M, Stein DR, Ferguson MA, Traum AZ, Soliman NA, Kari JA, El Desoky S, Fathy H, Zenker M, Bakkaloglu SA, Müller D, Noyan A, Ozaltin F, Cadnapaphornchai MA, Hashmi S, Hopcian J, Kopp JB, Benador N, Bockenhauer D, Bogdanovic R, Stajić N, Chernin G, Ettenger R, Fehrenbach H, Kemper M, Munarriz RL, Podracka L, Büscher R, Serdaroglu E, Tasic V, Mane S, Lifton RP, Braun DA, Hildebrandt F. Warejko JK, et al. Among authors: schmidt jm. Clin J Am Soc Nephrol. 2018 Jan 6;13(1):53-62. doi: 10.2215/CJN.04120417. Epub 2017 Nov 10. Clin J Am Soc Nephrol. 2018. PMID: 29127259 Free PMC article.
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
van der Ven AT, Connaughton DM, Ityel H, Mann N, Nakayama M, Chen J, Vivante A, Hwang DY, Schulz J, Braun DA, Schmidt JM, Schapiro D, Schneider R, Warejko JK, Daga A, Majmundar AJ, Tan W, Jobst-Schwan T, Hermle T, Widmeier E, Ashraf S, Amar A, Hoogstraaten CA, Hugo H, Kitzler TM, Kause F, Kolvenbach CM, Dai R, Spaneas L, Amann K, Stein DR, Baum MA, Somers MJG, Rodig NM, Ferguson MA, Traum AZ, Daouk GH, Bogdanović R, Stajić N, Soliman NA, Kari JA, El Desoky S, Fathy HM, Milosevic D, Al-Saffar M, Awad HS, Eid LA, Selvin A, Senguttuvan P, Sanna-Cherchi S, Rehm HL, MacArthur DG, Lek M, Laricchia KM, Wilson MW, Mane SM, Lifton RP, Lee RS, Bauer SB, Lu W, Reutter HM, Tasic V, Shril S, Hildebrandt F. van der Ven AT, et al. Among authors: schmidt jm. J Am Soc Nephrol. 2018 Sep;29(9):2348-2361. doi: 10.1681/ASN.2017121265. Epub 2018 Aug 24. J Am Soc Nephrol. 2018. PMID: 30143558 Free PMC article.
Gender Minority Stress: A Critical Review.
Tan KKH, Treharne GJ, Ellis SJ, Schmidt JM, Veale JF. Tan KKH, et al. Among authors: schmidt jm. J Homosex. 2020 Aug 23;67(10):1471-1489. doi: 10.1080/00918369.2019.1591789. Epub 2019 Mar 26. J Homosex. 2020. PMID: 30912709 Review.
Data collection and interpretation.
Citerio G, Park S, Schmidt JM, Moberg R, Suarez JI, Le Roux PD; Second Neurocritical Care Research Conference Investigators. Citerio G, et al. Among authors: schmidt jm. Neurocrit Care. 2015 Jun;22(3):360-8. doi: 10.1007/s12028-015-0139-4. Neurocrit Care. 2015. PMID: 25846711 Free article. Review.
Fluctuating selection and the determinants of genetic variation.
Johnson OL, Tobler R, Schmidt JM, Huber CD. Johnson OL, et al. Among authors: schmidt jm. Trends Genet. 2023 Jun;39(6):491-504. doi: 10.1016/j.tig.2023.02.004. Epub 2023 Mar 6. Trends Genet. 2023. PMID: 36890036 Free article. Review.
Can Generalist Predators Control Bemisia tabaci?
Kheirodin A, Simmons AM, Legaspi JC, Grabarczyk EE, Toews MD, Roberts PM, Chong JH, Snyder WE, Schmidt JM. Kheirodin A, et al. Among authors: schmidt jm. Insects. 2020 Nov 23;11(11):823. doi: 10.3390/insects11110823. Insects. 2020. PMID: 33238485 Free PMC article. Review.
Pediatric croup with COVID-19.
Venn AMR, Schmidt JM, Mullan PC. Venn AMR, et al. Among authors: schmidt jm. Am J Emerg Med. 2021 May;43:287.e1-287.e3. doi: 10.1016/j.ajem.2020.09.034. Epub 2020 Sep 15. Am J Emerg Med. 2021. PMID: 32980228 Free PMC article.
415 results