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

Year Number of Results
1951 1
1958 1
1981 2
1984 4
1985 3
1988 2
1990 1
1992 1
1993 2
1994 1
1996 1
1997 1
1998 1
1999 1
2000 1
2001 1
2002 5
2003 5
2004 3
2005 3
2006 1
2008 6
2009 1
2010 1
2011 1
2012 2
2013 6
2014 7
2015 4
2016 6
2017 7
2018 6
2019 9
2020 9
2021 8
2022 11
2023 9
2024 3

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125 results

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Page 1
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.
Sifrim A, Hitz MP, Wilsdon A, Breckpot J, Turki SH, Thienpont B, McRae J, Fitzgerald TW, Singh T, Swaminathan GJ, Prigmore E, Rajan D, Abdul-Khaliq H, Banka S, Bauer UM, Bentham J, Berger F, Bhattacharya S, Bu'Lock F, Canham N, Colgiu IG, Cosgrove C, Cox H, Daehnert I, Daly A, Danesh J, Fryer A, Gewillig M, Hobson E, Hoff K, Homfray T; INTERVAL Study; Kahlert AK, Ketley A, Kramer HH, Lachlan K, Lampe AK, Louw JJ, Manickara AK, Manase D, McCarthy KP, Metcalfe K, Moore C, Newbury-Ecob R, Omer SO, Ouwehand WH, Park SM, Parker MJ, Pickardt T, Pollard MO, Robert L, Roberts DJ, Sambrook J, Setchfield K, Stiller B, Thornborough C, Toka O, Watkins H, Williams D, Wright M, Mital S, Daubeney PE, Keavney B, Goodship J; UK10K Consortium; Abu-Sulaiman RM, Klaassen S, Wright CF, Firth HV, Barrett JC, Devriendt K, FitzPatrick DR, Brook JD; Deciphering Developmental Disorders Study; Hurles ME. Sifrim A, et al. Among authors: lampe ak. Nat Genet. 2016 Sep;48(9):1060-5. doi: 10.1038/ng.3627. Epub 2016 Aug 1. Nat Genet. 2016. PMID: 27479907 Free PMC article.
De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome.
Vetrini F, McKee S, Rosenfeld JA, Suri M, Lewis AM, Nugent KM, Roeder E, Littlejohn RO, Holder S, Zhu W, Alaimo JT, Graham B, Harris JM, Gibson JB, Pastore M, McBride KL, Komara M, Al-Gazali L, Al Shamsi A, Fanning EA, Wierenga KJ, Scott DA, Ben-Neriah Z, Meiner V, Cassuto H, Elpeleg O, Holder JL Jr, Burrage LC, Seaver LH, Van Maldergem L, Mahida S, Soul JS, Marlatt M, Matyakhina L, Vogt J, Gold JA, Park SM, Varghese V, Lampe AK, Kumar A, Lees M, Holder-Espinasse M, McConnell V, Bernhard B, Blair E, Harrison V; DDD study; Muzny DM, Gibbs RA, Elsea SH, Posey JE, Bi W, Lalani S, Xia F, Yang Y, Eng CM, Lupski JR, Liu P. Vetrini F, et al. Among authors: lampe ak. Genome Med. 2019 Feb 28;11(1):12. doi: 10.1186/s13073-019-0623-0. Genome Med. 2019. PMID: 30819258 Free PMC article.
Regulatory de novo mutations underlying intellectual disability.
De Vas MG, Boulet F, Joshi SS, Garstang MG, Khan TN, Atla G, Parry D, Moore D, Cebola I, Zhang S, Cui W, Lampe AK, Lam WW; Genomics England Research Consortium; Ferrer J, Pradeepa MM, Atanur SS. De Vas MG, et al. Among authors: lampe ak. Life Sci Alliance. 2023 Feb 28;6(5):e202201843. doi: 10.26508/lsa.202201843. Print 2023 May. Life Sci Alliance. 2023. PMID: 36854624 Free PMC article.
Trauma and trauma care in Europe.
Schäfer I, Hopchet M, Vandamme N, Ajdukovic D, El-Hage W, Egreteau L, Javakhishvili JD, Makhashvili N, Lampe A, Ardino V, Kazlauskas E, Mouthaan J, Sijbrandij M, Dragan M, Lis-Turlejska M, Figueiredo-Braga M, Sales L, Arnberg F, Nazarenko T, Nalyvaiko N, Armour C, Murphy D. Schäfer I, et al. Among authors: lampe a. Eur J Psychotraumatol. 2018 Dec 20;9(1):1556553. doi: 10.1080/20008198.2018.1556553. eCollection 2018. Eur J Psychotraumatol. 2018. PMID: 30637092 Free PMC article. Review.
[Genetics of Posttraumatic Stress Disorder (PTSD)].
Weiss EM, Parson W, Niederstätter H, Marksteiner J, Lampe A. Weiss EM, et al. Among authors: lampe a. Psychother Psychosom Med Psychol. 2019 Jul;69(7):266-274. doi: 10.1055/a-0634-6625. Epub 2018 Jul 19. Psychother Psychosom Med Psychol. 2019. PMID: 30025422 Review. German.
SOX5: Lamb-Shaffer syndrome-A case series further expanding the phenotypic spectrum.
Edgerley K, Bryson L, Hanington L, Irving R, Joss S, Lampe A, Maystadt I, Osio D, Richardson R, Split M, Sansbury FH, Scurr I, Stewart H, McNeil A, Low K. Edgerley K, et al. Among authors: lampe a. Am J Med Genet A. 2023 May;191(5):1447-1458. doi: 10.1002/ajmg.a.63124. Epub 2023 Mar 2. Am J Med Genet A. 2023. PMID: 36861937
Guillain-Barré syndrome and SARS-CoV-2.
Lampe A, Winschel A, Lang C, Steiner T. Lampe A, et al. Neurol Res Pract. 2020;2(1):19. doi: 10.1186/s42466-020-00066-0. Epub 2020 Jul 8. Neurol Res Pract. 2020. PMID: 32835165 Free PMC article.
[Psychosocial factors in reproductive medicine].
Lampe A, Schüßler G. Lampe A, et al. Z Psychosom Med Psychother. 2015;61(4):309-26. doi: 10.13109/zptm.2015.61.4.309. Z Psychosom Med Psychother. 2015. PMID: 26646911 Review. German.
Mutation update for the PORCN gene.
Lombardi MP, Bulk S, Celli J, Lampe A, Gabbett MT, Ousager LB, van der Smagt JJ, Soller M, Stattin EL, Mannens MA, Smigiel R, Hennekam RC. Lombardi MP, et al. Among authors: lampe a. Hum Mutat. 2011 Jul;32(7):723-8. doi: 10.1002/humu.21505. Epub 2011 Jun 21. Hum Mutat. 2011. PMID: 21472892 Review.
125 results