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

Year Number of Results
1923 1
1924 2
1925 1
1927 1
1952 2
1954 1
1955 4
1956 2
1957 1
1958 1
1959 1
1960 2
1961 3
1962 3
1963 2
1964 4
1965 6
1966 5
1967 9
1968 5
1969 6
1970 1
1971 2
1972 3
1973 3
1974 2
1975 5
1976 1
1977 1
1978 2
1979 5
1980 6
1981 5
1982 4
1983 4
1984 8
1985 10
1986 8
1987 6
1988 7
1989 12
1990 2
1991 13
1992 18
1993 16
1994 11
1995 9
1996 23
1997 13
1998 16
1999 12
2000 15
2001 23
2002 17
2003 21
2004 32
2005 37
2006 34
2007 39
2008 35
2009 36
2010 41
2011 42
2012 54
2013 43
2014 54
2015 65
2016 56
2017 56
2018 50
2019 57
2020 45
2021 48
2022 46
2023 28
2024 27
2025 23
2026 20

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1,191 results

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Page 1
Loeys-Dietz Syndrome.
Velchev JD, Van Laer L, Luyckx I, Dietz H, Loeys B. Velchev JD, et al. Among authors: dietz h. Adv Exp Med Biol. 2021;1348:251-264. doi: 10.1007/978-3-030-80614-9_11. Adv Exp Med Biol. 2021. PMID: 34807423
Loeys-Dietz syndrome: 2026 updated care management primer.
MacCarrick G, Afifi RO, Allen R, Almpani K, Black JH 3rd, Boyce AM, Braverman AC, Cameron DE, Caplan J, Cervi E, Cha MJ, Christensen J, van de Laar IM, Demo E, Dewals W, Doyle AJ, Doyle JJ, Fischbein MP, Fleischer J, Fleischman F, Frischmeyer-Guerrerio PA, Guerrerio AL, Huguenard AL, Jani PH, Jordan CP, Kim HJ, Krebsová A, Kockova R, Lee JS, Lobner K, Narula N, Niknahad A, Neptune E, Pedroza AJ, Perry M, Richer J, Rios-Sanchez J, Roman MJ, Russo M, Schweber J, Shalhub S, Sorber R, Speed T, Sponseller PD, Vincent TL, Whelan A, Zeiler SR, Loeys B, Dietz HC 3rd. MacCarrick G, et al. Among authors: dietz hc 3rd. Genet Med. 2026 Jul;28(7):102577. doi: 10.1016/j.gim.2026.102577. Epub 2026 Apr 15. Genet Med. 2026. PMID: 41988792 Free article. Review.
Cardiovascular Management of Aortopathy in Children: A Scientific Statement From the American Heart Association.
Morris SA, Flyer JN, Yetman AT, Quezada E, Cappella ES, Dietz HC, Milewicz DM, Ouzounian M, Rigelsky CM, Tierney S, Lacro RV; American Heart Association Council on Lifelong Congenital Heart Disease and Heart Health in the Young (Young Hearts); Council on Cardiovascular and Stroke Nursing; Council on Peripheral Vascular Disease; Council on Cardiopulmonary, Critical Care, Perioperative and Resuscitation; and Council on Cardiovascular Surgery and Anesthesia. Morris SA, et al. Among authors: dietz hc. Circulation. 2024 Sep 10;150(11):e228-e254. doi: 10.1161/CIR.0000000000001265. Epub 2024 Aug 12. Circulation. 2024. PMID: 39129620 Free article. Review.
Loeys-Dietz syndrome: a primer for diagnosis and management.
MacCarrick G, Black JH 3rd, Bowdin S, El-Hamamsy I, Frischmeyer-Guerrerio PA, Guerrerio AL, Sponseller PD, Loeys B, Dietz HC 3rd. MacCarrick G, et al. Among authors: dietz hc 3rd. Genet Med. 2014 Aug;16(8):576-87. doi: 10.1038/gim.2014.11. Epub 2014 Feb 27. Genet Med. 2014. PMID: 24577266 Free PMC article. Review.
Loeys-Dietz Syndrome.
Loeys BL, Dietz HC. Loeys BL, et al. Among authors: dietz hc. 2008 Feb 28 [updated 2024 Sep 12]. In: Adam MP, Bick S, Mirzaa GM, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026. 2008 Feb 28 [updated 2024 Sep 12]. In: Adam MP, Bick S, Mirzaa GM, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026. PMID: 20301312 Free Books & Documents. Review.
Interpretation and classification of FBN1 variants associated with Marfan syndrome: consensus recommendations from the Clinical Genome Resource's FBN1 variant curation expert panel.
Drackley A, Somerville C, Arnaud P, Baudhuin LM, Hanna N, Kluge ML, Kotzer K, Boileau C, Bronicki L, Callewaert B, Cecchi A, Dietz H, Guo D, Harris S, Jarinova O, Lindsay M, Little L, Loeys B, MacCarrick G, Meester J, Milewicz D, Morisaki T, Morisaki H, Murdock D, Renard M, Richer J, Robert L, Ouzounian M, Van Laer L, De Backer J, Muiño-Mosquera L. Drackley A, et al. Among authors: dietz h. Genome Med. 2024 Dec 31;16(1):154. doi: 10.1186/s13073-024-01423-3. Genome Med. 2024. PMID: 39741318 Free PMC article.
FBN1-Related Marfan Syndrome.
Dietz H. Dietz H. 2001 Apr 18 [updated 2022 Feb 17]. In: Adam MP, Bick S, Mirzaa GM, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026. 2001 Apr 18 [updated 2022 Feb 17]. In: Adam MP, Bick S, Mirzaa GM, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026. PMID: 20301510 Free Books & Documents. Review.
A mutation update on the LDS-associated genes TGFB2/3 and SMAD2/3.
Schepers D, Tortora G, Morisaki H, MacCarrick G, Lindsay M, Liang D, Mehta SG, Hague J, Verhagen J, van de Laar I, Wessels M, Detisch Y, van Haelst M, Baas A, Lichtenbelt K, Braun K, van der Linde D, Roos-Hesselink J, McGillivray G, Meester J, Maystadt I, Coucke P, El-Khoury E, Parkash S, Diness B, Risom L, Scurr I, Hilhorst-Hofstee Y, Morisaki T, Richer J, Désir J, Kempers M, Rideout AL, Horne G, Bennett C, Rahikkala E, Vandeweyer G, Alaerts M, Verstraeten A, Dietz H, Van Laer L, Loeys B. Schepers D, et al. Among authors: dietz h. Hum Mutat. 2018 May;39(5):621-634. doi: 10.1002/humu.23407. Epub 2018 Mar 6. Hum Mutat. 2018. PMID: 29392890 Free PMC article.
ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm.
Gould RA, Aziz H, Woods CE, Seman-Senderos MA, Sparks E, Preuss C, Wünnemann F, Bedja D, Moats CR, McClymont SA, Rose R, Sobreira N, Ling H, MacCarrick G, Kumar AA, Luyckx I, Cannaerts E, Verstraeten A, Björk HM, Lehsau AC, Jaskula-Ranga V, Lauridsen H, Shah AA, Bennett CL, Ellinor PT, Lin H, Isselbacher EM, Lino Cardenas CL, Butcher JT, Hughes GC, Lindsay ME; Baylor-Hopkins Center for Mendelian Genomics; MIBAVA Leducq Consortium; Mertens L, Franco-Cereceda A, Verhagen JMA, Wessels M, Mohamed SA, Eriksson P, Mital S, Van Laer L, Loeys BL, Andelfinger G, McCallion AS, Dietz HC. Gould RA, et al. Among authors: dietz hc. Nat Genet. 2019 Jan;51(1):42-50. doi: 10.1038/s41588-018-0265-y. Epub 2018 Nov 19. Nat Genet. 2019. PMID: 30455415 Free PMC article.
Loeys-Dietz syndrome.
Van Laer L, Dietz H, Loeys B. Van Laer L, et al. Among authors: dietz h. Adv Exp Med Biol. 2014;802:95-105. doi: 10.1007/978-94-007-7893-1_7. Adv Exp Med Biol. 2014. PMID: 24443023 Review.
1,191 results