Fulya Taylan (F Taylan)

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 26

Top Venues

EMBO molecular medicine

NPJ genomic medicine

Blood advances

American journal of medical genetics. Part A

Karolinska Universitetssjukhuset

Boğaziçi Üniversitesi (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Karolinska Universitetssjukhuset Jun 01 2020

Sweden

Coordinator :: Clinical genetics

Education History

Boğaziçi Üniversitesi

Turkey

PHD :: Molecular Biology and Genetics

Boğaziçi Üniversitesi

Turkey

MSC :: Molecular Biology and Genetics

Boğaziçi Üniversitesi

Turkey

BSC :: Molecular Biology and Genetics

Publications

Sailan Wang, Pernilla Nikamo, Leena Laasonen, Bjorn Gudbjornsson, Leif Ejstrup, Lars Iversen, Ulla Lindqvist, Jessica J Alm, Jesper Eisfeldt, Xiaowei Zheng, Sergiu-Bogdan Catrina, Fulya Taylan, Raquel Vaz, Mona Ståhle, Isabel Tapia-Paez
Rare coding variants in NOX4 link high ROS levels to psoriatic arthritis mutilans. EMBO molecular medicine (2024)
Sailan Wang, Pernilla Nikamo, Leena Laasonen, Bjorn Gudbjornsson, Leif Ejstrup, Lars Iversen, Ulla Lindqvist, Jessica J Alm, Jesper Eisfeldt, Xiaowei Zheng, Sergiu-Bogdan Catrina, Fulya Taylan, Raquel Vaz, Mona Ståhle, Isabel Tapia-Paez
Rare coding variants in NOX4 link high ROS levels to psoriatic arthritis mutilans. EMBO molecular medicine 16 (3) (2024)
Sailan Wang, Pernilla Nikamo, Leena Laasonen, Bjorn Gudbjornsson, Leif Ejstrup, Lars Iversen, Ulla Lindqvist, Jessica J Alm, Jesper Eisfeldt, Xiaowei Zheng, Sergiu-Bogdan Catrina, Fulya Taylan, Raquel Vaz, Mona Ståhle, Isabel Tapia-Paez
Rare coding variants in NOX4 link high ROS levels to psoriatic arthritis mutilans. EMBO molecular medicine 16 (3) (2024)
Carolina Maya-González, Giorgio Tettamanti, Fulya Taylan, Anna Skarin Nordenvall, Thomas Sejersen, Ann Nordgren
Cancer Risk in Patients With Muscular Dystrophy and Myotonic Dystrophy: A Register-Based Cohort Study. Neurology 103 (8) (2024)
Sailan Wang, Pernilla Nikamo, Leena Laasonen, Bjorn Gudbjornsson, Leif Ejstrup, Lars Iversen, Ulla Lindqvist, Jessica J Alm, Jesper Eisfeldt, Xiaowei Zheng, Sergiu-Bogdan Catrina, Fulya Taylan, Raquel Vaz, Mona Ståhle, Isabel Tapia-Paez
Rare coding variants in NOX4 link high ROS levels to psoriatic arthritis mutilans. EMBO molecular medicine 16 (3) (2024)
Emma Elizabeth Palmer, Helene Cederroth, Mikk Cederroth, Angelica Maria Delgado-Vega, Natalie Roberts, Fulya Taylan, Ann Nordgren, Lorenzo D Botto
Equity in action: The Diagnostic Working Group of The Undiagnosed Diseases Network International. NPJ genomic medicine 9 (1) (2024)
Carolina Maya-González, Angelica Maria Delgado-Vega, Fulya Taylan, Kristina Lagerstedt Robinson, Lina Hansson, Niklas Pal, Henrik Fagman, Florian Puls, Sandra Wessman, Jakob Stenman, Kleopatra Georgantzi, Susanne Fransson, Teresita Díaz De Ståhl, Torben Ek, Ruth Palmer, Bianca Tesi, Per Kogner, Tommy Martinsson, Ann Nordgren
Occurrence of cancer in Marfan syndrome: Report of two patients with neuroblastoma and review of the literature. American journal of medical genetics. Part A (2024)
Emma Elizabeth Palmer, Helene Cederroth, Mikk Cederroth, Angelica Maria Delgado-Vega, Natalie Roberts, Fulya Taylan, Ann Nordgren, Lorenzo D Botto
Equity in action: The Diagnostic Working Group of The Undiagnosed Diseases Network International. NPJ genomic medicine 9 (1) (2024)
Sailan Wang, Pernilla Nikamo, Leena Laasonen, Bjorn Gudbjornsson, Leif Ejstrup, Lars Iversen, Ulla Lindqvist, Jessica J Alm, Jesper Eisfeldt, Xiaowei Zheng, Sergiu-Bogdan Catrina, Fulya Taylan, Raquel Vaz, Mona Ståhle, Isabel Tapia-Paez
Rare coding variants in NOX4 link high ROS levels to psoriatic arthritis mutilans. EMBO molecular medicine 16 (3) (2024)
Emma Elizabeth Palmer, Helene Cederroth, Mikk Cederroth, Angelica Maria Delgado-Vega, Natalie Roberts, Fulya Taylan, Ann Nordgren, Lorenzo D Botto
Equity in action: The Diagnostic Working Group of The Undiagnosed Diseases Network International. NPJ genomic medicine 9 (1) (2024)
Dominyka Batkovskyte, Fiona McKenzie, Fulya Taylan, Pelin Ozlem Simsek-Kiper, Sarah M Nikkel, Hirofumi Ohashi, Roger E Stevenson, Thuong Ha, Denise P Cavalcanti, Hiroyuki Miyahara, Steven A Skinner, Miguel A Aguirre, Zühal Akçören, Gulen Eda Utine, Tillie Chiu, Kenji Shimizu, Anna Hammarsjö, Koray Boduroglu, Hannah W Moore, Raymond J Louie, Peer Arts, Allie N Merrihew, Milena Babic, Matilda R Jackson, Nikos Papadogiannakis, Anna Lindstrand, Ann Nordgren, Christopher P Barnett, Hamish S Scott, Andrei S Chagin, Gen Nishimura, Giedre Grigelioniene
Al-Gazali skeletal dysplasia constitutes the lethal end of ADAMTSL2-related disorders. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research (2023)
Elisabeth Wadensten, Sandra Wessman, Frida Abel, Teresita Díaz de Ståhl, Bianca Tesi, Christina Orsmark Pietras, Linda Arvidsson, Fulya Taylan, Susanne Fransson, Hartmut Vogt, Anna Poluha, Sailendra Pradhananga, Maria Hellberg, Kristina Lagerstedt-Robinson, Praveen Raj Somarajan, Sofie Samuelsson, Sara Orrsjö, Khurram Maqbool, Karin Henning, Tobias Strid, Torben Ek, Henrik Fagman, Thomas Olsson Bontell, Tommy Martinsson, Florian Puls, Per Kogner, Valtteri Wirta, Cornelis J H Pronk, Joakim Wille, Richard Rosenquist, Monica Nistér, Fredrik Mertens, Magnus Sabel, Ulrika Norén-Nyström, Pernilla Grillner, Ann Nordgren, Gustaf Ljungman, Johanna Sandgren, David Gisselsson, null null
Diagnostic Yield From a Nationwide Implementation of Precision Medicine for all Children With Cancer. JCO precision oncology 7 (2023)
Ela Curic, Lisa Jean Ewans, Ryan Pysar, Fulya Taylan, Lorenzo D Botto, Ann Nordgren, William A Gahl, Emma Elizabeth Palmer
International Undiagnosed Diseases Programs (UDPs): components and outcomes. Orphanet journal of rare diseases 18 (1) (2023)
Benedicte Bang, Jesper Eisfeldt, Gisela Barbany, Arja H Harila-Saari, Mats Heyman, Vasilios Zachariadis, Fulya Taylan, Ann Nordgren
A somatic UBA2 variant preceded ETV6-RUNX1 in the concordant BCP-ALL of monozygotic twins. Blood advances 6 (7) (2022)
Sofia Frisk, Alexandra Wachtmeister, Tobias Laurell, Anna Lindstrand, Nina Jäntti, Helena Malmgren, Kristina Lagerstedt-Robinson, Bianca Tesi, Fulya Taylan, Ann Nordgren
Detection of germline mosaicism in fathers of children with intellectual disability syndromes caused by de novo variants. Molecular genetics & genomic medicine 10 (4) (2022)
Mari Muurinen, Fulya Taylan, Symeon Tournis, Jesper Eisfeldt, Alexia Balanika, Heleni Vastardis, Sirpa Ala-Mello, Outimaija Mäkitie, Alice Costantini
Mosaic Deletions of Known Genes Explain Skeletal Dysplasias With High and Low Bone Mass. JBMR plus 6 (8) (2022)
Anna Hammarsjö, Maria Pettersson, David Chitayat, Atsuhiko Handa, Britt-Marie Anderlid, Marco Bartocci, Donald Basel, Dominyka Batkovskyte, Ana Beleza-Meireles, Peter Conner, Jesper Eisfeldt, Katta M Girisha, Brian Hon-Yin Chung, Eva Horemuzova, Hironobu Hyodo, Liene Korņejeva, Kristina Lagerstedt-Robinson, Angela E Lin, Måns Magnusson, Shahida Moosa, Shalini S Nayak, Daniel Nilsson, Hirofumi Ohashi, Naoko Ohashi-Fukuda, Henrik Stranneheim, Fulya Taylan, Rasa Traberg, Ulrika Voss, Valtteri Wirta, Ann Nordgren, Gen Nishimura, Anna Lindstrand, Giedre Grigelioniene
High diagnostic yield in skeletal ciliopathies using massively parallel genome sequencing, structural variant screening and RNA analyses. Journal of human genetics 66 (10) (2021)
Tekla Harju, Benedicte Bang, Vasilios Zachariadis, Fulya Taylan, Jukka S Moilanen, Merja Möttönen, Carl Inge Edvard Smith, Arja H Harila-Saari, Riitta Niinimäki, Ann Nordgren
Predisposition to childhood acute lymphoblastic leukemia caused by a constitutional translocation disrupting ETV6. Blood advances 3 (18) (2020)
Emeli Pontén, Sofia Frisk, Fulya Taylan, Raquel Vaz, Sandra Wessman, Leanne de Kock, Niklas Pal, William D Foulkes, Kristina Lagerstedt-Robinson, Ann Nordgren
A complex DICER1 syndrome phenotype associated with a germline pathogenic variant affecting the RNase IIIa domain of DICER1. Journal of medical genetics (2020)
Sofia Frisk, Fulya Taylan, Izabela Blaszczyk, Inger Nennesmo, Göran Annerén, Bettina Herm, Eva-Lena Stattin, Vasilios Zachariadis, Anna Lindstrand, Bianca Tesi, Tobias Laurell, Ann Nordgren
Early activating somatic PIK3CA mutations promote ectopic muscle development and upper limb overgrowth. Clinical genetics 96 (2) (2019)
Giedre Grigelioniene, Hiroshi I Suzuki, Fulya Taylan, Fatemeh Mirzamohammadi, Zvi U Borochowitz, Ugur M Ayturk, Shay Tzur, Eva Horemuzova, Anna Lindstrand, Mary Ann Weis, Gintautas Grigelionis, Anna Hammarsjö, Elin Marsk, Ann Nordgren, Magnus Nordenskjöld, David R Eyre, Matthew L Warman, Gen Nishimura, Phillip A Sharp, Tatsuya Kobayashi
Gain-of-function mutation of microRNA-140 in human skeletal dysplasia. Nature medicine 25 (4) (2019)
Ingegerd Öfverholm, Vasilios Zachariadis, Fulya Taylan, Yanara Marincevic-Zuniga, Anh Nhi Tran, Leonie Saft, Daniel Nilsson, Ann-Christine Syvänen, Gudmar Lönnerholm, Arja Harila-Saari, Magnus Nordenskjöld, Mats Heyman, Ann Nordgren, Jessica Nordlund, Gisela Barbany
Overexpression of chromatin remodeling and tyrosine kinase genes in iAMP21-positive acute lymphoblastic leukemia. Leukemia & lymphoma 61 (3) (2019)
Malin Kvarnung, Fulya Taylan, Daniel Nilsson, Britt-Marie Anderlid, Helena Malmgren, Kristina Lagerstedt-Robinson, Eva Holmberg, Magnus Burstedt, Magnus Nordenskjöld, Ann Nordgren, Elisabeth S Lundberg
Genomic screening in rare disorders: New mutations and phenotypes, highlighting ALG14 as a novel cause of severe intellectual disability. Clinical genetics 94 (6) (2018)
Alice Costantini, Panagiotis Ν Krallis, Anders Kämpe, Emmanouil M Karavitakis, Fulya Taylan, Outi Mäkitie, Artemis Doulgeraki
A novel frameshift deletion in PLS3 causing severe primary osteoporosis. Journal of human genetics 63 (8) (2018)
A Hammarsjö, Z Wang, R Vaz, Fulya Taylan, M Sedghi, K M Girisha, D Chitayat, K Neethukrishna, P Shannon, R Godoy, K Gowrishankar, A Lindstrand, J Nasiri, M Baktashian, P T Newton, L Guo, W Hofmeister, M Pettersson, Andrei S Chagin, G Nishimura, L Yan, N Matsumoto, A Nordgren, N Miyake, G Grigelioniene, S Ikegawa
Novel KIAA0753 mutations extend the phenotype of skeletal ciliopathies. Scientific reports 7 (1) (2017)
Fulya Taylan, Zehra Yavaş Abalı, Nina Jäntti, Nilay Güneş, Feyza Darendeliler, Firdevs Baş, Şükran Poyrazoğlu, Nevbahar Tamçelik, Beyhan Tüysüz, Outi Mäkitie
Two novel mutations in XYLT2 cause spondyloocular syndrome. American journal of medical genetics. Part A 173 (12) (2017)

Fulya Taylan.css-eqlu8i{font-size:small;padding-left:4px;} (F Taylan)

Publication Activity (10 Years)

Top Topics

Top Venues

Fulya Taylan (F Taylan)