Michael Levy - London Health Sciences Centre

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Papers共 61 篇Author StatisticsCo-AuthorSimilar Experts

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Epigenomic and Phenotypic Characterization of DEGCAGS Syndrome

Karim Karimi,Denisa Weis,Ingvild Aukrust,Tzung-Chien Hsieh, Marie Horackova,Julie Paulsen,Roberto Mendoza Londono,Lucie Dupuis, Megan Dickson, Hellen Lesman,Tracy Lau,David Murphy, Khalid Hama Salih, Bassam M. S. Al-Musawi, Ruqayah G. Y. Al-Obaidi,Malgorzata Rydzanicz, Mateus Biela, Mafalda Saraiva Santos, Abdulrahman Aldeeri,Hanna T. Gazda,Lynn Pais,Shirlee Shril,Henrik Dollner,Sandip Bartakke,Franco Laccone,Andrea Soltysova,Thomas Kitzler,Neveen A. Soliman,Raissa Relator,Michael A. Levy,Jennifer Kerkhof,Jessica Rzasa,Henry Houlden, Gabriela V. Pilshofer, Tilman Jobst-Schwan,Friedhelm Hildebrandt,Sergio B. Sousa,Reza Maroofian,Timothy W. Yu,Peter Krawitz,Bekim Sadikovic,Sofia Douzgou Houge

European journal of human genetics EJHGno. 12 (2024): 1574-1582

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Clinico-biological Refinement of BCL11B-related Disorder and Identification of an Episignature: A Series of 20 Unreported Individuals

Quentin Sabbagh,Sadegheh Haghshenas,Juliette Piard,Chloe Trouve,Jeanne Amiel,Tania Attie-Bitach,Tugce Balci,Mouna Barat-Houari,Alyce Belonis,Odile Boute,Diana S. Brightman,Ange-Line Bruel,Stefano Giuseppe Caraffi,Nicolas Chatron,Corinne Collet,William Dufour,Patrick Edery,Chin-To Fong,Carlo Fusco,Vincent Gatinois,Evan Gouy,Anne-Marie Guerrot,Solveig Heide, Aakash Joshi,Natalya Karp,Boris Keren,Marion Lesieur-Sebellin,Jonathan Levy,Michael A. Levy,Claire Lozano,Stanislas Lyonnet,Henri Margot,Pauline Marzin,Haley Mcconkey,Vincent Michaud,Gael Nicolas, Mevyn Nizard, Alix Paulet,Francesca Peluso,Vincent Pernin,Laurence Perrin,Christophe Philippe,Chitra Prasad,Madhavi Prasad,Raissa Relator,Marlene Rio,Sophie Rondeau,Valentin Ruault,Nathalie Ruiz-Pallares,Elodie Sanchez,Debbie Shears,Victoria Mok Siu,Arthur Sorlin,Matthew Tedder,Mylene Tharreau,Frederic Tran Mau-Them,Liselot van der Laan,Julien Van Gils,Alain Verloes,Sandra Whalen,Marjolaine Willems,Kevin Yauy,Roberta Zuntini,Jennifer Kerkhof,Bekim Sadikovic,David Genevieve

GENETICS IN MEDICINEno. 1 (2024)

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Liselot van der Laan, Ananília Silva,Lotte Kleinendorst,Kathleen Rooney,Sadegheh Haghshenas,Peter Lauffer, Yasemin Alanay,Pratibha Bhai,Alfredo Brusco, Sonja de Munnik,Bert B A de Vries, Angelica Delgado Vega, Marc Engelen,Johanna C Herkert,Ron Hochstenbach,Saskia Hopman,Sarina G Kant,Ryutaro Kira,Mitsuhiro Kato, Boris Keren,Hester Y Kroes,Michael A Levy,Ngu Lock-Hock,Saskia M Maas, Grazia M S Mancini,Carlo Marcelis,Naomichi Matsumoto,Takeshi Mizuguchi,Alessandro Mussa, Cyril Mignot, Anu Närhi, Ann Nordgren, Rolph Pfundt, Abeltje M Polstra,Slavica Trajkova,Yolande van Bever, Marie José van den Boogaard,Jasper J van der Smagt, Tahsin Stefan Barakat,Mariëlle Alders,Marcel M A M Mannens,Bekim Sadikovic,Mieke M van Haelst,Peter Henneman

HGG advancesno. 1 (2024): 100380-100380

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Identification of a DNA Methylation Episignature for Recurrent Constellations of Embryonic Malformations

AMERICAN JOURNAL OF HUMAN GENETICSno. 8 (2024)

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The Detection of a Strong Episignature for Chung–Jansen Syndrome, Partially Overlapping with Börjeson–Forssman–Lehmann and White–Kernohan Syndromes

Niels Vos,Sadegheh Haghshenas,Liselot van der Laan, Perle K. M. Russel,Kathleen Rooney,Michael A. Levy,Raissa Relator,Jennifer Kerkhof,Haley McConkey,Saskia M. Maas,Lisenka E. L. M. Vissers,Bert B. A. de Vries,Rolph Pfundt,Mariet W. Elting,Johanna M. van Hagen,Nienke E. Verbeek,Marjolijn C. J. Jongmans,Phillis Lakeman,Lynne Rumping,Danielle G. M. Bosch,Antonio Vitobello,Christel Thauvin-Robinet,Laurence Faivre,Sophie Nambot,Aurore Garde,Marjolaine Willems,David Genevieve,Gaël Nicolas,Tiffany Busa,Annick Toutain,Marion Gérard,Varoona Bizaoui,Bertrand Isidor,Giuseppe Merla,Maria Accadia,Charles E. Schwartz,Katrin Ounap,Mariëtte J. V. Hoffer,Marjan M. Nezarati,Marie-José H. van den Boogaard,Matthew L. Tedder,Curtis Rogers,Alfredo Brusco,Giovanni B. Ferrero,Marta Spodenkiewicz,Richard Sidlow,Alessandro Mussa,Slavica Trajkova,Emma McCann,Henry J. Mroczkowski,Sandra Jansen,Laura Donker-Kaat,Floor A. M. Duijkers,Kyra E. Stuurman,Marcel M. A. M. Mannens,Mariëlle Alders,Peter Henneman,Susan M. White,Bekim Sadikovic,Mieke M. van Haelst

Human Geneticspp.1-13, (2024)

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