Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia

Aline Verstraeten; Melanie H. A. M. Perik; Anna A. Baranowska; Josephina A. N. Meester; Lotte Van Den Heuvel; Jarl Bastianen; Marlies Kempers; Ingrid P. C. Krapels; Angela Maas; Andrea Rideout; Anthony Vandersteen; Glenda Sobey; Diana Johnson; Erik Fransen; Neeti Ghali; Tom Webb; Abtehale Al-Hussaini; Peter de Leeuw; Philippe Delmotte; Marilucy Lopez-Sublet; Marco Pappaccogli; Muriel Sprynger; Laurent Toubiana; Lut Van Laer; Fleur S. Van Dijk; Miikka Vikkula; Nilesh J. Samani; Alexandre Persu; David Adlam; Bart Loeys; European/International Fibromuscular Dysplasia Registry and Initiative (FEIRI)

doi:10.1161/CIRCULATIONAHA.120.045946

Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia

Aline Verstraeten, Melanie H. A. M. Perik, Anna A. Baranowska, Josephina A. N. Meester, Lotte Van Den Heuvel, Jarl Bastianen, Marlies Kempers, Ingrid P. C. Krapels, Angela Maas, Andrea Rideout, Anthony Vandersteen, Glenda Sobey, Diana Johnson, Erik Fransen, Neeti Ghali, Tom Webb, Abtehale Al-Hussaini, Peter de Leeuw, Philippe Delmotte, Marilucy Lopez-SubletMarco Pappaccogli, Muriel Sprynger, Laurent Toubiana, Lut Van Laer, Fleur S. Van Dijk, Miikka Vikkula, Nilesh J. Samani, Alexandre Persu, David Adlam^*, Bart Loeys^*, European/International Fibromuscular Dysplasia Registry and Initiative (FEIRI)

^*Corresponding author for this work

Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review

Original language	English
Pages (from-to)	1021-1024
Number of pages	4
Journal	Circulation
Volume	142
Issue number	10
DOIs	https://doi.org/10.1161/CIRCULATIONAHA.120.045946
Publication status	Published - 8 Sept 2020

Keywords

coronary artery disease
fibromuscular dysplasia
genetics
Loeys-Dietz syndrome

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10.1161/CIRCULATIONAHA.120.045946Licence: CC BY

Cite this

Verstraeten, A., Perik, M. H. A. M., Baranowska, A. A., Meester, J. A. N., Van Den Heuvel, L., Bastianen, J., Kempers, M., Krapels, I. P. C., Maas, A., Rideout, A., Vandersteen, A., Sobey, G., Johnson, D., Fransen, E., Ghali, N., Webb, T., Al-Hussaini, A., de Leeuw, P., Delmotte, P., ... European/International Fibromuscular Dysplasia Registry and Initiative (FEIRI) (2020). Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia. Circulation, 142(10), 1021-1024. https://doi.org/10.1161/CIRCULATIONAHA.120.045946

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title = "Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia",

keywords = "coronary artery disease, fibromuscular dysplasia, genetics, Loeys-Dietz syndrome",

author = "Aline Verstraeten and Perik, {Melanie H. A. M.} and Baranowska, {Anna A.} and Meester, {Josephina A. N.} and {Van Den Heuvel}, Lotte and Jarl Bastianen and Marlies Kempers and Krapels, {Ingrid P. C.} and Angela Maas and Andrea Rideout and Anthony Vandersteen and Glenda Sobey and Diana Johnson and Erik Fransen and Neeti Ghali and Tom Webb and Abtehale Al-Hussaini and {de Leeuw}, Peter and Philippe Delmotte and Marilucy Lopez-Sublet and Marco Pappaccogli and Muriel Sprynger and Laurent Toubiana and {Van Laer}, Lut and {Van Dijk}, {Fleur S.} and Miikka Vikkula and Samani, {Nilesh J.} and Alexandre Persu and David Adlam and Bart Loeys and {European/International Fibromuscular Dysplasia Registry and Initiative (FEIRI)}",

year = "2020",

month = sep,

day = "8",

doi = "10.1161/CIRCULATIONAHA.120.045946",

language = "English",

volume = "142",

pages = "1021--1024",

journal = "Circulation",

issn = "0009-7322",

publisher = "Lippincott Williams & Wilkins",

number = "10",

}

Verstraeten, A, Perik, MHAM, Baranowska, AA, Meester, JAN, Van Den Heuvel, L, Bastianen, J, Kempers, M, Krapels, IPC, Maas, A, Rideout, A, Vandersteen, A, Sobey, G, Johnson, D, Fransen, E, Ghali, N, Webb, T, Al-Hussaini, A, de Leeuw, P, Delmotte, P, Lopez-Sublet, M, Pappaccogli, M, Sprynger, M, Toubiana, L, Van Laer, L, Van Dijk, FS, Vikkula, M, Samani, NJ, Persu, A, Adlam, D, Loeys, B & European/International Fibromuscular Dysplasia Registry and Initiative (FEIRI) 2020, 'Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia', Circulation, vol. 142, no. 10, pp. 1021-1024. https://doi.org/10.1161/CIRCULATIONAHA.120.045946

Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia. / Verstraeten, Aline; Perik, Melanie H. A. M.; Baranowska, Anna A. et al.
In: Circulation, Vol. 142, No. 10, 08.09.2020, p. 1021-1024.

Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review

TY - JOUR

T1 - Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia

AU - Verstraeten, Aline

AU - Perik, Melanie H. A. M.

AU - Baranowska, Anna A.

AU - Meester, Josephina A. N.

AU - Van Den Heuvel, Lotte

AU - Bastianen, Jarl

AU - Kempers, Marlies

AU - Krapels, Ingrid P. C.

AU - Maas, Angela

AU - Rideout, Andrea

AU - Vandersteen, Anthony

AU - Sobey, Glenda

AU - Johnson, Diana

AU - Fransen, Erik

AU - Ghali, Neeti

AU - Webb, Tom

AU - Al-Hussaini, Abtehale

AU - de Leeuw, Peter

AU - Delmotte, Philippe

AU - Lopez-Sublet, Marilucy

AU - Pappaccogli, Marco

AU - Sprynger, Muriel

AU - Toubiana, Laurent

AU - Van Laer, Lut

AU - Van Dijk, Fleur S.

AU - Vikkula, Miikka

AU - Samani, Nilesh J.

AU - Persu, Alexandre

AU - Adlam, David

AU - Loeys, Bart

AU - European/International Fibromuscular Dysplasia Registry and Initiative (FEIRI)

PY - 2020/9/8

Y1 - 2020/9/8

KW - coronary artery disease

KW - fibromuscular dysplasia

KW - genetics

KW - Loeys-Dietz syndrome

U2 - 10.1161/CIRCULATIONAHA.120.045946

DO - 10.1161/CIRCULATIONAHA.120.045946

M3 - Comment/Letter to the editor

C2 - 32897753

SN - 0009-7322

VL - 142

SP - 1021

EP - 1024

JO - Circulation

JF - Circulation

IS - 10

ER -