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Results by year

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

Year Number of Results
1880 1
1884 2
1888 2
1889 2
1890 2
1894 1
1899 1
1900 2
1902 1
1904 2
1906 1
1908 1
1909 1
1910 3
1911 1
1977 1
1978 2
1981 1
1982 1
1986 3
1987 2
1988 4
1989 3
1990 2
1991 5
1992 6
1993 6
1994 8
1995 4
1996 4
1997 3
1998 2
1999 4
2000 4
2001 2
2002 6
2003 4
2005 2
2006 3
2007 3
2009 3
2010 5
2011 4
2012 3
2013 1
2014 4
2015 3
2016 2
2017 5
2018 3
2019 2
2020 3
2021 5
2022 2
2024 0

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Article attribute

Article type

Publication date

Search Results

143 results

Results by year

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Page 1
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.
Fu JM, Satterstrom FK, Peng M, Brand H, Collins RL, Dong S, Wamsley B, Klei L, Wang L, Hao SP, Stevens CR, Cusick C, Babadi M, Banks E, Collins B, Dodge S, Gabriel SB, Gauthier L, Lee SK, Liang L, Ljungdahl A, Mahjani B, Sloofman L, Smirnov AN, Barbosa M, Betancur C, Brusco A, Chung BHY, Cook EH, Cuccaro ML, Domenici E, Ferrero GB, Gargus JJ, Herman GE, Hertz-Picciotto I, Maciel P, Manoach DS, Passos-Bueno MR, Persico AM, Renieri A, Sutcliffe JS, Tassone F, Trabetti E, Campos G, Cardaropoli S, Carli D, Chan MCY, Fallerini C, Giorgio E, Girardi AC, Hansen-Kiss E, Lee SL, Lintas C, Ludena Y, Nguyen R, Pavinato L, Pericak-Vance M, Pessah IN, Schmidt RJ, Smith M, Costa CIS, Trajkova S, Wang JYT, Yu MHC; Autism Sequencing Consortium (ASC); Broad Institute Center for Common Disease Genomics (Broad-CCDG); iPSYCH-BROAD Consortium; Cutler DJ, De Rubeis S, Buxbaum JD, Daly MJ, Devlin B, Roeder K, Sanders SJ, Talkowski ME. Fu JM, et al. Among authors: herman ge. Nat Genet. 2022 Sep;54(9):1320-1331. doi: 10.1038/s41588-022-01104-0. Epub 2022 Aug 18. Nat Genet. 2022. PMID: 35982160 Free PMC article.
ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG).
Miller DT, Lee K, Chung WK, Gordon AS, Herman GE, Klein TE, Stewart DR, Amendola LM, Adelman K, Bale SJ, Gollob MH, Harrison SM, Hershberger RE, McKelvey K, Richards CS, Vlangos CN, Watson MS, Martin CL; ACMG Secondary Findings Working Group. Miller DT, et al. Among authors: herman ge. Genet Med. 2021 Aug;23(8):1381-1390. doi: 10.1038/s41436-021-01172-3. Epub 2021 May 20. Genet Med. 2021. PMID: 34012068 Free article. No abstract available.
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG).
Miller DT, Lee K, Gordon AS, Amendola LM, Adelman K, Bale SJ, Chung WK, Gollob MH, Harrison SM, Herman GE, Hershberger RE, Klein TE, McKelvey K, Richards CS, Vlangos CN, Stewart DR, Watson MS, Martin CL; ACMG Secondary Findings Working Group. Miller DT, et al. Among authors: herman ge. Genet Med. 2021 Aug;23(8):1391-1398. doi: 10.1038/s41436-021-01171-4. Epub 2021 May 20. Genet Med. 2021. PMID: 34012069 Free article. No abstract available.
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Kalia SS, Adelman K, Bale SJ, Chung WK, Eng C, Evans JP, Herman GE, Hufnagel SB, Klein TE, Korf BR, McKelvey KD, Ormond KE, Richards CS, Vlangos CN, Watson M, Martin CL, Miller DT. Kalia SS, et al. Among authors: herman ge. Genet Med. 2017 Feb;19(2):249-255. doi: 10.1038/gim.2016.190. Epub 2016 Nov 17. Genet Med. 2017. PMID: 27854360 Free article.
Mouse X chromosome.
Brown SD, Avner P, Herman GE. Brown SD, et al. Among authors: herman ge. Mamm Genome. 1992;3 Spec No:S274-88. doi: 10.1007/BF00648438. Mamm Genome. 1992. PMID: 1498440 Review. No abstract available.
Mouse X chromosome.
Brown SD, Avner P, Chapman VM, Hamvas RM, Herman GE. Brown SD, et al. Among authors: herman ge. Mamm Genome. 1991;1 Spec No:S318-31. doi: 10.1007/BF00656501. Mamm Genome. 1991. PMID: 1799807 Review. No abstract available.
Inborn errors of sterol biosynthesis.
Kelley RI, Herman GE. Kelley RI, et al. Among authors: herman ge. Annu Rev Genomics Hum Genet. 2001;2:299-341. doi: 10.1146/annurev.genom.2.1.299. Annu Rev Genomics Hum Genet. 2001. PMID: 11701653 Review.
The role of ZIC3 in vertebrate development.
Herman GE, El-Hodiri HM. Herman GE, et al. Cytogenet Genome Res. 2002;99(1-4):229-35. doi: 10.1159/000071598. Cytogenet Genome Res. 2002. PMID: 12900569 Review.
143 results