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Robust validation of methylation levels association at CPT1A locus with lipid plasma levels.

Journal of lipid research

Gagnon F, Aïssi D, Carrié A, Morange PE, Trégouët DA.
PMID: 24850808
J Lipid Res. 2014 Jul;55(7):1189-91. doi: 10.1194/jlr.E051276. Epub 2014 May 21.

No abstract available.

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Gagnon F, Aïssi D, Carrié A, et al. Robust validation of methylation levels association at CPT1A locus with lipid plasma levels. J Lipid Res. 2014;55(7):1189-91doi: 10.1194/jlr.E051276.
Gagnon, F., Aïssi, D., Carrié, A., Morange, P. E., & Trégouët, D. A. (2014). Robust validation of methylation levels association at CPT1A locus with lipid plasma levels. Journal of lipid research, 55(7), 1189-91. https://doi.org/10.1194/jlr.E051276
Gagnon, France, et al. "Robust validation of methylation levels association at CPT1A locus with lipid plasma levels." Journal of lipid research vol. 55,7 (2014): 1189-91. doi: https://doi.org/10.1194/jlr.E051276
Gagnon F, Aïssi D, Carrié A, Morange PE, Trégouët DA. Robust validation of methylation levels association at CPT1A locus with lipid plasma levels. J Lipid Res. 2014 Jul;55(7):1189-91. doi: 10.1194/jlr.E051276. Epub 2014 May 21. PMID: 24850808; PMCID: PMC4076097.
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Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.

Nature communications

Guéant JL, Chéry C, Oussalah A, Nadaf J, Coelho D, Josse T, Flayac J, Robert A, Koscinski I, Gastin I, Filhine-Tresarrieu P, Pupavac M, Brebner A, Watkins D, Pastinen T, Montpetit A, Hariri F, Tregouët D, Raby BA, Chung WK, Morange PE, Froese DS, Baumgartner MR, Benoist JF, Ficicioglu C, Marchand V, Motorin Y, Bonnemains C, Feillet F, Majewski J, Rosenblatt DS.
PMID: 29396438
Nat Commun. 2018 Feb 02;9(1):554. doi: 10.1038/s41467-018-03054-w.

The original version of this Article contained an error in the title, which was incorrectly given as 'APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients'. This has now been corrected in both the PDF and HTML...

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Guéant JL, Chéry C, Oussalah A, et al. Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients. Nat Commun. 2018;9(1):554doi: 10.1038/s41467-018-03054-w.
Guéant, J. L., Chéry, C., Oussalah, A., Nadaf, J., Coelho, D., Josse, T., Flayac, J., Robert, A., Koscinski, I., Gastin, I., Filhine-Tresarrieu, P., Pupavac, M., Brebner, A., Watkins, D., Pastinen, T., Montpetit, A., Hariri, F., Tregouët, D., Raby, B. A., Chung, W. K., Morange, P. E., Froese, D. S., Baumgartner, M. R., Benoist, J. F., Ficicioglu, C., Marchand, V., Motorin, Y., Bonnemains, C., Feillet, F., Majewski, J., & Rosenblatt, D. S. (2018). Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients. Nature communications, 9(1), 554. https://doi.org/10.1038/s41467-018-03054-w
Guéant, Jean-Louis, et al. "Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients." Nature communications vol. 9,1 (2018): 554. doi: https://doi.org/10.1038/s41467-018-03054-w
Guéant JL, Chéry C, Oussalah A, Nadaf J, Coelho D, Josse T, Flayac J, Robert A, Koscinski I, Gastin I, Filhine-Tresarrieu P, Pupavac M, Brebner A, Watkins D, Pastinen T, Montpetit A, Hariri F, Tregouët D, Raby BA, Chung WK, Morange PE, Froese DS, Baumgartner MR, Benoist JF, Ficicioglu C, Marchand V, Motorin Y, Bonnemains C, Feillet F, Majewski J, Rosenblatt DS. Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients. Nat Commun. 2018 Feb 02;9(1):554. doi: 10.1038/s41467-018-03054-w. PMID: 29396438; PMCID: PMC5797229.
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Effects of Thyroid Function on Hemostasis, Coagulation, and Fibrinolysis: A Mendelian Randomization Study.

Thyroid : official journal of the American Thyroid Association

Ellervik C, Mora S, Kuś A, Åsvold B, Marouli E, Deloukas P, Sterenborg RBTM, Teumer A, Burgess S, Sabater-Lleal M, Huffman J, Johnson AD, Trégouet DA, Smith NL, Medici M, DeVries PS, Chasman DI, Kjaergaard AD.
PMID: 34210154
Thyroid. 2021 Sep;31(9):1305-1315. doi: 10.1089/thy.2021.0055. Epub 2021 Aug 05.

No abstract available.

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Ellervik C, Mora S, Kuś A, et al. Effects of Thyroid Function on Hemostasis, Coagulation, and Fibrinolysis: A Mendelian Randomization Study. Thyroid. 2021;31(9):1305-1315doi: 10.1089/thy.2021.0055.
Ellervik, C., Mora, S., Kuś, A., Åsvold, B., Marouli, E., Deloukas, P., Sterenborg, R. B. T. M., Teumer, A., Burgess, S., Sabater-Lleal, M., Huffman, J., Johnson, A. D., Trégouet, D. A., Smith, N. L., Medici, M., DeVries, P. S., Chasman, D. I., & Kjaergaard, A. D. (2021). Effects of Thyroid Function on Hemostasis, Coagulation, and Fibrinolysis: A Mendelian Randomization Study. Thyroid : official journal of the American Thyroid Association, 31(9), 1305-1315. https://doi.org/10.1089/thy.2021.0055
Ellervik, Christina, et al. "Effects of Thyroid Function on Hemostasis, Coagulation, and Fibrinolysis: A Mendelian Randomization Study." Thyroid : official journal of the American Thyroid Association vol. 31,9 (2021): 1305-1315. doi: https://doi.org/10.1089/thy.2021.0055
Ellervik C, Mora S, Kuś A, Åsvold B, Marouli E, Deloukas P, Sterenborg RBTM, Teumer A, Burgess S, Sabater-Lleal M, Huffman J, Johnson AD, Trégouet DA, Smith NL, Medici M, DeVries PS, Chasman DI, Kjaergaard AD. Effects of Thyroid Function on Hemostasis, Coagulation, and Fibrinolysis: A Mendelian Randomization Study. Thyroid. 2021 Sep;31(9):1305-1315. doi: 10.1089/thy.2021.0055. Epub 2021 Aug 05. PMID: 34210154; PMCID: PMC8558080.
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Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation.

Blood

Goumidi L, Thibord F, Wiggins KL, Li-Gao R, Brown MR, van Hylckama Vlieg A, Souto JC, Soria JM, Ibrahim-Kosta M, Saut N, Daian D, Olaso R, Amouyel P, Debette S, Boland A, Bailly P, Morrison AC, Mook-Kanamori DO, Deleuze JF, Johnson A, de Vries PS, Sabater-Lleal M, Chiaroni J, Smith NL, Rosendaal FR, Chasman DI, Trégouët DA, Morange PE.
PMID: 33512453
Blood. 2021 Apr 29;137(17):2394-2402. doi: 10.1182/blood.2020008997.

Genetic risk score (GRS) analysis is a popular approach to derive individual risk prediction models for complex diseases. In venous thrombosis (VT), such type of analysis shall integrate information at the ABO blood group locus, which is one of...

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Goumidi L, Thibord F, Wiggins KL, et al. Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation. Blood. 2021;137(17):2394-2402doi: 10.1182/blood.2020008997.
Goumidi, L., Thibord, F., Wiggins, K. L., Li-Gao, R., Brown, M. R., van Hylckama Vlieg, A., Souto, J. C., Soria, J. M., Ibrahim-Kosta, M., Saut, N., Daian, D., Olaso, R., Amouyel, P., Debette, S., Boland, A., Bailly, P., Morrison, A. C., Mook-Kanamori, D. O., Deleuze, J. F., Johnson, A., de Vries, P. S., Sabater-Lleal, M., Chiaroni, J., Smith, N. L., Rosendaal, F. R., Chasman, D. I., Trégouët, D. A., & Morange, P. E. (2021). Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation. Blood, 137(17), 2394-2402. https://doi.org/10.1182/blood.2020008997
Goumidi, Louisa, et al. "Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation." Blood vol. 137,17 (2021): 2394-2402. doi: https://doi.org/10.1182/blood.2020008997
Goumidi L, Thibord F, Wiggins KL, Li-Gao R, Brown MR, van Hylckama Vlieg A, Souto JC, Soria JM, Ibrahim-Kosta M, Saut N, Daian D, Olaso R, Amouyel P, Debette S, Boland A, Bailly P, Morrison AC, Mook-Kanamori DO, Deleuze JF, Johnson A, de Vries PS, Sabater-Lleal M, Chiaroni J, Smith NL, Rosendaal FR, Chasman DI, Trégouët DA, Morange PE. Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation. Blood. 2021 Apr 29;137(17):2394-2402. doi: 10.1182/blood.2020008997. PMID: 33512453; PMCID: PMC8085481.
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Probing the adsorption/desorption of amphiphilic polymers at the air-water interface during large interfacial deformations.

Soft matter

Trégouët C, Salez T, Pantoustier N, Perrin P, Reyssat M, Monteux C.
PMID: 31328760
Soft Matter. 2019 Aug 14;15(30):6200-6206. doi: 10.1039/c9sm00368a. Epub 2019 Jul 22.

Hydrophobically modified polymers are good candidates for the stabilization of liquid interfaces thanks to the high anchoring energy of the hydrophobic parts. In this article we probe the interfacial anchoring of a series of home-made hydrophobically modified polymers with...

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Trégouët C, Salez T, Pantoustier N, et al. Probing the adsorption/desorption of amphiphilic polymers at the air-water interface during large interfacial deformations. Soft Matter. 2019;15(30):6200-6206doi: 10.1039/c9sm00368a.
Trégouët, C., Salez, T., Pantoustier, N., Perrin, P., Reyssat, M., & Monteux, C. (2019). Probing the adsorption/desorption of amphiphilic polymers at the air-water interface during large interfacial deformations. Soft matter, 15(30), 6200-6206. https://doi.org/10.1039/c9sm00368a
Trégouët, C, et al. "Probing the adsorption/desorption of amphiphilic polymers at the air-water interface during large interfacial deformations." Soft matter vol. 15,30 (2019): 6200-6206. doi: https://doi.org/10.1039/c9sm00368a
Trégouët C, Salez T, Pantoustier N, Perrin P, Reyssat M, Monteux C. Probing the adsorption/desorption of amphiphilic polymers at the air-water interface during large interfacial deformations. Soft Matter. 2019 Aug 14;15(30):6200-6206. doi: 10.1039/c9sm00368a. Epub 2019 Jul 22. PMID: 31328760.
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Adsorption dynamics of hydrophobically modified polymers at an air-water interface.

The European physical journal. E, Soft matter

Trégouët C, Mikhailovskaya A, Salez T, Pantoustier N, Perrin P, Reyssat M, Monteux C.
PMID: 30182262
Eur Phys J E Soft Matter. 2018 Sep 06;41(9):101. doi: 10.1140/epje/i2018-11711-y.

Using surface-tension measurements, we study the brush-limited adsorption dynamics of a range of amphiphilic polymers, PAAH-[Formula: see text]-[Formula: see text] composed of a poly(acrylic acid) backbone, PAAH, grafted with a fraction [Formula: see text] of alkyl moieties, containing either...

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Trégouët C, Mikhailovskaya A, Salez T, et al. Adsorption dynamics of hydrophobically modified polymers at an air-water interface. Eur Phys J E Soft Matter. 2018;41(9):101doi: 10.1140/epje/i2018-11711-y.
Trégouët, C., Mikhailovskaya, A., Salez, T., Pantoustier, N., Perrin, P., Reyssat, M., & Monteux, C. (2018). Adsorption dynamics of hydrophobically modified polymers at an air-water interface. The European physical journal. E, Soft matter, 41(9), 101. https://doi.org/10.1140/epje/i2018-11711-y
Trégouët, C, et al. "Adsorption dynamics of hydrophobically modified polymers at an air-water interface." The European physical journal. E, Soft matter vol. 41,9 (2018): 101. doi: https://doi.org/10.1140/epje/i2018-11711-y
Trégouët C, Mikhailovskaya A, Salez T, Pantoustier N, Perrin P, Reyssat M, Monteux C. Adsorption dynamics of hydrophobically modified polymers at an air-water interface. Eur Phys J E Soft Matter. 2018 Sep 06;41(9):101. doi: 10.1140/epje/i2018-11711-y. PMID: 30182262.
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Microfluidic probing of the complex interfacial rheology of multilayer capsules.

Soft matter

Trégouët C, Salez T, Monteux C, Reyssat M.
PMID: 30887970
Soft Matter. 2019 Apr 07;15(13):2782-2790. doi: 10.1039/c8sm02507j. Epub 2019 Mar 19.

Encapsulation of chemicals using polymer membranes enables control of their transport and delivery for applications such as agrochemistry or detergency. To rationalize the design of polymer capsules, it is necessary to understand how the membranes' mechanical properties control the...

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Trégouët C, Salez T, Monteux C, et al. Microfluidic probing of the complex interfacial rheology of multilayer capsules. Soft Matter. 2019;15(13):2782-2790doi: 10.1039/c8sm02507j.
Trégouët, C., Salez, T., Monteux, C., & Reyssat, M. (2019). Microfluidic probing of the complex interfacial rheology of multilayer capsules. Soft matter, 15(13), 2782-2790. https://doi.org/10.1039/c8sm02507j
Trégouët, Corentin, et al. "Microfluidic probing of the complex interfacial rheology of multilayer capsules." Soft matter vol. 15,13 (2019): 2782-2790. doi: https://doi.org/10.1039/c8sm02507j
Trégouët C, Salez T, Monteux C, Reyssat M. Microfluidic probing of the complex interfacial rheology of multilayer capsules. Soft Matter. 2019 Apr 07;15(13):2782-2790. doi: 10.1039/c8sm02507j. Epub 2019 Mar 19. PMID: 30887970.
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Bayesian network analysis of plasma microRNA sequencing data in patients with venous thrombosis.

European heart journal supplements : journal of the European Society of Cardiology

Thibord F, Munsch G, Perret C, Suchon P, Roux M, Ibrahim-Kosta M, Goumidi L, Deleuze JF, Morange PE, Trégouët DA.
PMID: 32368197
Eur Heart J Suppl. 2020 Apr;22:C34-C45. doi: 10.1093/eurheartj/suaa008. Epub 2020 Apr 29.

MicroRNAs (miRNAs) are small regulatory RNAs participating to several biological processes and known to be involved in various pathologies. Measurable in body fluids, miRNAs have been proposed to serve as efficient biomarkers for diseases and/or associated traits. Here, we...

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Thibord F, Munsch G, Perret C, et al. Bayesian network analysis of plasma microRNA sequencing data in patients with venous thrombosis. Eur Heart J Suppl. 2020;22:C34-C45doi: 10.1093/eurheartj/suaa008.
Thibord, F., Munsch, G., Perret, C., Suchon, P., Roux, M., Ibrahim-Kosta, M., Goumidi, L., Deleuze, J. F., Morange, P. E., & Trégouët, D. A. (2020). Bayesian network analysis of plasma microRNA sequencing data in patients with venous thrombosis. European heart journal supplements : journal of the European Society of Cardiology, 22C34-C45. https://doi.org/10.1093/eurheartj/suaa008
Thibord, Florian, et al. "Bayesian network analysis of plasma microRNA sequencing data in patients with venous thrombosis." European heart journal supplements : journal of the European Society of Cardiology vol. 22 (2020): C34-C45. doi: https://doi.org/10.1093/eurheartj/suaa008
Thibord F, Munsch G, Perret C, Suchon P, Roux M, Ibrahim-Kosta M, Goumidi L, Deleuze JF, Morange PE, Trégouët DA. Bayesian network analysis of plasma microRNA sequencing data in patients with venous thrombosis. Eur Heart J Suppl. 2020 Apr;22:C34-C45. doi: 10.1093/eurheartj/suaa008. Epub 2020 Apr 29. PMID: 32368197; PMCID: PMC7189740.
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Association of Coding Variants in Hydroxysteroid 17-beta Dehydrogenase 14 (.

Journal of the American Society of Nephrology : JASN

Mychaleckyj JC, Valo E, Ichimura T, Ahluwalia TS, Dina C, Miller RG, Shabalin IG, Gyorgy B, Cao J, Onengut-Gumuscu S, Satake E, Smiles AM, Haukka JK, Tregouet DA, Costacou T, O'Neil K, Paterson AD, Forsblom C, Keenan HA, Pezzolesi MG, Pragnell M, Galecki A, Rich SS, Sandholm N, Klein R, Klein BE, Susztak K, Orchard TJ, Korstanje R, King GL, Hadjadj S, Rossing P, Bonventre JV, Groop PH, Warram JH, Krolewski AS.
PMID: 34261756
J Am Soc Nephrol. 2021 Oct;32(10):2634-2651. doi: 10.1681/ASN.2020101457. Epub 2021 Jul 14.

No abstract available.

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Mychaleckyj JC, Valo E, Ichimura T, et al. Association of Coding Variants in Hydroxysteroid 17-beta Dehydrogenase 14 (. J Am Soc Nephrol. 2021;32(10):2634-2651doi: 10.1681/ASN.2020101457.
Mychaleckyj, J. C., Valo, E., Ichimura, T., Ahluwalia, T. S., Dina, C., Miller, R. G., Shabalin, I. G., Gyorgy, B., Cao, J., Onengut-Gumuscu, S., Satake, E., Smiles, A. M., Haukka, J. K., Tregouet, D. A., Costacou, T., O'Neil, K., Paterson, A. D., Forsblom, C., Keenan, H. A., Pezzolesi, M. G., Pragnell, M., Galecki, A., Rich, S. S., Sandholm, N., Klein, R., Klein, B. E., Susztak, K., Orchard, T. J., Korstanje, R., King, G. L., Hadjadj, S., Rossing, P., Bonventre, J. V., Groop, P. H., Warram, J. H., & Krolewski, A. S. (2021). Association of Coding Variants in Hydroxysteroid 17-beta Dehydrogenase 14 (. Journal of the American Society of Nephrology : JASN, 32(10), 2634-2651. https://doi.org/10.1681/ASN.2020101457
Mychaleckyj, Josyf C, et al. "Association of Coding Variants in Hydroxysteroid 17-beta Dehydrogenase 14 (." Journal of the American Society of Nephrology : JASN vol. 32,10 (2021): 2634-2651. doi: https://doi.org/10.1681/ASN.2020101457
Mychaleckyj JC, Valo E, Ichimura T, Ahluwalia TS, Dina C, Miller RG, Shabalin IG, Gyorgy B, Cao J, Onengut-Gumuscu S, Satake E, Smiles AM, Haukka JK, Tregouet DA, Costacou T, O'Neil K, Paterson AD, Forsblom C, Keenan HA, Pezzolesi MG, Pragnell M, Galecki A, Rich SS, Sandholm N, Klein R, Klein BE, Susztak K, Orchard TJ, Korstanje R, King GL, Hadjadj S, Rossing P, Bonventre JV, Groop PH, Warram JH, Krolewski AS. Association of Coding Variants in Hydroxysteroid 17-beta Dehydrogenase 14 (. J Am Soc Nephrol. 2021 Oct;32(10):2634-2651. doi: 10.1681/ASN.2020101457. Epub 2021 Jul 14. PMID: 34261756.
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NPTX1 mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxia.

Brain : a journal of neurology

Coutelier M, Jacoupy M, Janer A, Renaud F, Auger N, Saripella GV, Ancien F, Pucci F, Rooman M, Gilis D, Larivière R, Sgarioto N, Valter R, Guillot-Noel L, Le Ber I, Sayah S, Charles P, Nümann A, Pauly MG, Helmchen C, Deininger N, Haack TB, Brais B, Brice A, Trégouët DA, El Hachimi KH, Shoubridge EA, Durr A, Stevanin G.
PMID: 34788392
Brain. 2021 Nov 11; doi: 10.1093/brain/awab407. Epub 2021 Nov 11.

With more than forty causative genes identified so far, autosomal dominant cerebellar ataxias exhibit a remarkable genetic heterogeneity. Yet, half the patients are lacking a molecular diagnosis. In a large family with nine sampled affected members, we performed exome...

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Coutelier M, Jacoupy M, Janer A, et al. NPTX1 mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxia. Brain. 2021;doi: 10.1093/brain/awab407.
Coutelier, M., Jacoupy, M., Janer, A., Renaud, F., Auger, N., Saripella, G. V., Ancien, F., Pucci, F., Rooman, M., Gilis, D., Larivière, R., Sgarioto, N., Valter, R., Guillot-Noel, L., Le Ber, I., Sayah, S., Charles, P., Nümann, A., Pauly, M. G., Helmchen, C., Deininger, N., Haack, T. B., Brais, B., Brice, A., Trégouët, D. A., El Hachimi, K. H., Shoubridge, E. A., Durr, A., & Stevanin, G. (2021). NPTX1 mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxia. Brain : a journal of neurology, . https://doi.org/10.1093/brain/awab407
Coutelier, Marie, et al. "NPTX1 mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxia." Brain : a journal of neurology vol. (2021). doi: https://doi.org/10.1093/brain/awab407
Coutelier M, Jacoupy M, Janer A, Renaud F, Auger N, Saripella GV, Ancien F, Pucci F, Rooman M, Gilis D, Larivière R, Sgarioto N, Valter R, Guillot-Noel L, Le Ber I, Sayah S, Charles P, Nümann A, Pauly MG, Helmchen C, Deininger N, Haack TB, Brais B, Brice A, Trégouët DA, El Hachimi KH, Shoubridge EA, Durr A, Stevanin G. NPTX1 mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxia. Brain. 2021 Nov 11; doi: 10.1093/brain/awab407. Epub 2021 Nov 11. PMID: 34788392.
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The prevalence of lumbar disc degeneration in symptomatic younger patients: A study of MRI scans.

Journal of clinical orthopaedics and trauma

Berg AJ, Ahmadje U, Jayanna HH, Trégouët P, Sanville P, Kapoor V.
PMID: 32879583
J Clin Orthop Trauma. 2020 Sep-Oct;11(5):932-936. doi: 10.1016/j.jcot.2020.07.021. Epub 2020 Jul 28.

STUDY DESIGN: Retrospective Cohort Study.OBJECTIVE: Low back pain (LBP) and radiculopathy present a significant burden to patients and healthcare systems. Lumbar disc degeneration (LDD) is associated with LBP. While the prevalence of LDD in older, symptomatic, patients has been...

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Berg AJ, Ahmadje U, Jayanna HH, et al. The prevalence of lumbar disc degeneration in symptomatic younger patients: A study of MRI scans. J Clin Orthop Trauma. 2020;11(5):932-936doi: 10.1016/j.jcot.2020.07.021.
Berg, A. J., Ahmadje, U., Jayanna, H. H., Trégouët, P., Sanville, P., & Kapoor, V. (2020). The prevalence of lumbar disc degeneration in symptomatic younger patients: A study of MRI scans. Journal of clinical orthopaedics and trauma, 11(5), 932-936. https://doi.org/10.1016/j.jcot.2020.07.021
Berg, Andrew James, et al. "The prevalence of lumbar disc degeneration in symptomatic younger patients: A study of MRI scans." Journal of clinical orthopaedics and trauma vol. 11,5 (2020): 932-936. doi: https://doi.org/10.1016/j.jcot.2020.07.021
Berg AJ, Ahmadje U, Jayanna HH, Trégouët P, Sanville P, Kapoor V. The prevalence of lumbar disc degeneration in symptomatic younger patients: A study of MRI scans. J Clin Orthop Trauma. 2020 Sep-Oct;11(5):932-936. doi: 10.1016/j.jcot.2020.07.021. Epub 2020 Jul 28. PMID: 32879583; PMCID: PMC7452323.
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Whole blood levels of S1PR4 mRNA associated with cerebral vasospasm after aneurysmal subarachnoid hemorrhage.

Journal of neurosurgery

Pulcrano-Nicolas AS, Jacquens A, Proust C, Clarençon F, Perret C, Shotar E, Puybasset L, Le Goff W, Degos V, Trégouët DA, Garnier S.
PMID: 31783362
J Neurosurg. 2019 Nov 29;1-5. doi: 10.3171/2019.9.JNS191305. Epub 2019 Nov 29.

OBJECTIVE: The authors sought to identify mRNA biomarkers of cerebral vasospasm in whole blood of patients suffering from aneurysmal subarachnoid hemorrhage (aSAH).METHODS: A prospective transcriptomic study for vasospasm was conducted in whole blood samples of 44 aSAH patients who...

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Pulcrano-Nicolas AS, Jacquens A, Proust C, et al. Whole blood levels of S1PR4 mRNA associated with cerebral vasospasm after aneurysmal subarachnoid hemorrhage. J Neurosurg. 2019;1-5doi: 10.3171/2019.9.JNS191305.
Pulcrano-Nicolas, A. S., Jacquens, A., Proust, C., Clarençon, F., Perret, C., Shotar, E., Puybasset, L., Le Goff, W., Degos, V., Trégouët, D. A., & Garnier, S. (2019). Whole blood levels of S1PR4 mRNA associated with cerebral vasospasm after aneurysmal subarachnoid hemorrhage. Journal of neurosurgery, 1-5. https://doi.org/10.3171/2019.9.JNS191305
Pulcrano-Nicolas, Anne-Sophie, et al. "Whole blood levels of S1PR4 mRNA associated with cerebral vasospasm after aneurysmal subarachnoid hemorrhage." Journal of neurosurgery vol. (2019): 1-5. doi: https://doi.org/10.3171/2019.9.JNS191305
Pulcrano-Nicolas AS, Jacquens A, Proust C, Clarençon F, Perret C, Shotar E, Puybasset L, Le Goff W, Degos V, Trégouët DA, Garnier S. Whole blood levels of S1PR4 mRNA associated with cerebral vasospasm after aneurysmal subarachnoid hemorrhage. J Neurosurg. 2019 Nov 29;1-5. doi: 10.3171/2019.9.JNS191305. Epub 2019 Nov 29. PMID: 31783362.
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