Czakó Marta
1 Papers
Czakó Marta is an academic researcher. The author has contributed to research in topics: Gene & Breakpoint. The author has an hindex of 1, co-authored 1 publications.
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Papers
Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders
Chelsea Lowther,Mana M. Mehrjouy,Ryan L. Collins,Mads Bak,Olga Dudchenko,Harrison Brand,Zirui Dong,Malene B. Rasmussen,Huiya Gu,David Weisz,Lusine Nazaryan-Petersen,Amanda S Fjorder,Yuan Mang,Allan Lind-Thomsen,Juan M M Mendez,Xabier Calle,Anu Chopra,C.R. Hansen,Merete Bugge,R. V. Broekema,Teppo Varilo,Tiia Maria Luukkonen,J. J. M. Engelen,Angela Maria Vianna-Morgante,Ana Carolina S. Fonseca,Juliana F. Mazzeu,H. Dornelles-Wawruk,Kikue Terada Abe,Joris Vermeesch,Kris Van Den Bogaert,Carolina Sismani,Constantia Aristidou,Paola Evangelidou,Albert Schinzel,Damien Sanlaville,Caroline Schluth-Bolard,Vera M. Kalscheuer,Maren Wenzel,Hyung Goo Kim,Katrin Õunap,Laura Roht,Susanna Midyan,Maria Clara Bonaglia,Anna Lindstrand,Jesper Eisfeldt,Jesper Ottosson,Daniel Nilsson,Maria Pettersson,Elenice Ferreira Bastos,Evica Rajcan-Separovic,Fatma Silan,Frenny Sheth,Antonio Novelli,Eirik Frengen,Madeleine Fannemel,Petter Strømme,Nadja Kokalj Vokac,Cornelia Daumer-Haas,Danilo Moretti-Ferreira,Deise Helena de Souza,Maria A. Ramos-Arroyo,Maria M. Igoa,Lyudmila Angelova,Peter M. Kroisel,Graciela Del Rey,Társis Paiva Vieira,Suzanne M E Lewis,Wang Hao,Jana Drabova,Marketa Havlovicova,Miroslava Hancarova,Zdenek Sedlacek,Ida Vogel,Tina Duelund Hjortshøj,Rikke S. Møller,Zeynep Tümer,Christina Fagerberg,Lilian Bomme Ousager,Bitten Schönewolf-Greulich,Mathilde Faurholdt Lauridsen,Juliette Piard,Céline Pebrel-Richard,Sylvie Jaillard,Nadja Ehmke,Eunice G Stefanou,Czakó Marta,Kosztolányi György,Ashwin Dalal,Usha Dutta,Rashmi G. Shukla,Fortunato Lonardo,Orsetta Zuffardi,Gunnar Houge,Doriana Misceo,Shahid Mahmood Baig,Alina T. Midro,Natalia Wawrusiewicz-Kurylonek,Isabel M. Carreira,Joana B. Melo,Laura Rodriguez Martinez,Miriam Guitart,Lovisa Lovmar,Jacob Gullander,Kerstin Hansson,Cynthia de Almeida Estéves,Yassmine Akkari,Jacqueline R. Batanian,Xu Li,James Lespinasse,Asli Silahtaroglu,Christina Halgren Harding,Lotte Nylandsted Krogh,Juliet M. Taylor,Klaus Lehnert,Rosamund Hill,Russell G. Snell,Christophe Samson,Jessie C. Jacobsen,Brynn Levy,Ozden Altiok Clark,Asli Toylu,Banu Güzel Nur,Ercan Mihci,Kathryn O’Keefe,Kiana Mohajeri-Stickels,E Wilch,Tammy Kammin,Raul E. Piña-Aguilar,Katarena Nalbandian,Sehime Gulsun Temel,Sebnem Ozemri Sag,Burcu Turkgenc,Arveen Kamath,Adriana Ruiz-Herrera,Siddharth Banka,Samantha L.P. Schilit,Benjamin Currall,Naomi Yachelevich,S. Galloway,Wendy K. Chung,Salmo Raskin,Idit Maya,Naama Orenstein,Nesia Kropach Gilad,Kayla Flamenbaum,Beverly N. Hay,Cynthia C. Morton,Eric Liao,Kwong Wai Choy,James F. Gusella,Peter B. Jacky,Erez Lieberman Aiden,Iben Bache,Michael E. Talkowski,Niels Tommerup +154 more
TL;DR: The results emphasize the potential impact of noncoding structural variants to cause LRPEs in unsolved DD cases, as well as the complex interaction of features associated with predicting intolerance to alteration of three-dimensional chromatin topology.