Works by Dikoglu, Esra

Results: 12

Co-Occurrence of Familial Non-Medullary Thyroid Cancer (FNMTC) and Hereditary Non-Polyposis Colorectal Cancer (HNPCC) Associated Tumors—A Cohort Study.

Published in:

Frontiers in Endocrinology, 2021, v. 12, p. 1, doi. 10.3389/fendo.2021.653401

By:

Aswath, Kshama;
Welch, James;
Gubbi, Sriram;
Veeraraghavan, Padmasree;
Avadhanula, Shirisha;
Gara, Sudheer Kumar;
Dikoglu, Esra;
Merino, Maria;
Raffeld, Mark;
Xi, Liqiang;
Kebebew, Electron;
Klubo-Gwiezdzinska, Joanna

Publication type:

Article

Correction to: Sequencing and curation strategies for identifying candidate glioblastoma treatments.

Published in:

2019

By:

Frank, Mayu O.;
Koyama, Takahiko;
Rhrissorrakrai, Kahn;
Robine, Nicolas;
Utro, Filippo;
Emde, Anne-Katrin;
Chen, Bo-Juen;
Arora, Kanika;
Shah, Minita;
Geiger, Heather;
Felice, Vanessa;
Dikoglu, Esra;
Rahman, Sadia;
Fang, Xiaolan;
Vacic, Vladimir;
Bergmann, Ewa A.;
Moore Vogel, Julia L.;
Reeves, Catherine;
Khaira, Depinder;
Calabro, Anthony

Publication type:

Correction Notice

Sequencing and curation strategies for identifying candidate glioblastoma treatments.

Published in:

BMC Medical Genomics, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s12920-019-0500-0

By:

Frank, Mayu O.;
Koyama, Takahiko;
Rhrissorrakrai, Kahn;
Robine, Nicolas;
Utro, Filippo;
Emde, Anne-Katrin;
Chen, Bo-Juen;
Arora, Kanika;
Shah, Minita;
Geiger, Heather;
Felice, Vanessa;
Dikoglu, Esra;
Rahman, Sadia;
Fang, Alice;
Vacic, Vladimir;
Bergmann, Ewa A.;
Vogel, Julia L. Moore;
Reeves, Catherine;
Khaira, Depinder;
Calabro, Anthony

Publication type:

Article

'Case of the Month' from the National Cancer Institute, Bethesda, MD, USA: investigating genetic aberrations in a patient with high‐risk prostate cancer.

Published in:

BJU International, 2021, v. 127, n. 2, p. 171, doi. 10.1111/bju.15273

By:

O'Connor, Luke P.;
Lebastchi, Amir H.;
Fasaye, Grace‐Ann;
Dikoglu, Esra;
Daneshvar, Michael A.;
Ahdoot, Michael;
Merino, Maria J.;
Pinto, Peter A.

Publication type:

Article

Extending the mutation spectrum for Galloway-Mowat syndrome to include homozygous missense mutations in the WDR73 gene.

Published in:

American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 4, p. 992, doi. 10.1002/ajmg.a.37533

By:

Rosti, Rasim O.;
Dikoglu, Esra;
Zaki, Maha S.;
Abdel‐Salam, Ghada;
Makhseed, Nawal;
Sese, Jordan C.;
Musaev, Damir;
Rosti, Basak;
Harbert, Mary J.;
Jones, Marilyn C.;
Vaux, Keith K.;
Gleeson, Joseph G.

Publication type:

Article

Mutations in LONP1, a mitochondrial matrix protease, cause CODAS syndrome.

Published in:

American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 7, p. 1501, doi. 10.1002/ajmg.a.37029

By:

Dikoglu, Esra;
Alfaiz, Ali;
Gorna, Maria;
Bertola, Deborah;
Chae, Jong Hee;
Cho, Tae‐Joon;
Derbent, Murat;
Alanay, Yasemin;
Guran, Tulay;
Kim, Ok‐Hwa;
Llerenar Jr, Juan C.;
Yamamoto, Guillerme;
Superti‐Furga, Giulio;
Reymond, Alexandre;
Xenarios, Ioannis;
Stevenson, Brian;
Campos‐Xavier, Belinda;
Bonafé, Luisa;
Superti‐Furga, Andrea;
Unger, Sheila

Publication type:

Article

Positive effects of an angiotensin II type 1 receptor antagonist in Camurati-Engelmann disease: A single case observation.

Published in:

American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 10, p. 2667, doi. 10.1002/ajmg.a.36692

By:

Simsek‐Kiper, Pelin Ozlem;
Dikoglu, Esra;
Campos‐Xavier, Belinda;
Utine, Gulen Eda;
Bonafe, Luisa;
Unger, Sheila;
Boduroglu, Koray;
Superti‐Furga, Andrea

Publication type:

Article

Homozygosity for a novel truncating mutation confirms TBX15 deficiency as the cause of Cousin syndrome.

Published in:

American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 12, p. 3161, doi. 10.1002/ajmg.a.36173

By:

Dikoglu, Esra;
Simsek‐Kiper, Pelin Ozlem;
Utine, Gulen Eda;
Campos‐Xavier, Belinda;
Boduroglu, Koray;
Bonafé, Luisa;
Superti‐Furga, Andrea;
Unger, Sheila

Publication type:

Article

PYCR2 Mutations cause a lethal syndrome of microcephaly and failure to thrive.

Published in:

2016

By:

Zaki, Maha S.;
Bhat, Gifty;
Sultan, Tipu;
Issa, Mahmoud;
Jung, Hea‐Jin;
Dikoglu, Esra;
Selim, Laila;
G. Mahmoud, Imam;
Abdel‐Hamid, Mohamed S.;
Abdel‐Salam, Ghada;
Marin‐Valencia, Isaac;
Gleeson, Joseph G.;
Jung, Hea-Jin;
Abdel-Hamid, Mohamed S;
Abdel-Salam, Ghada;
Marin-Valencia, Isaac

Publication type:

journal article

Mutations in the heat-shock protein A9 (HSPA9) gene cause the EVEN-PLUS syndrome of congenital malformations and skeletal dysplasia.

Published in:

Scientific Reports, 2015, p. 17154, doi. 10.1038/srep17154

By:

Royer-Bertrand, Beryl;
Castillo-Taucher, Silvia;
Moreno-Salinas, Rodrigo;
Cho, Tae-Joon;
Chae, Jong-Hee;
Choi, Murim;
Kim, Ok-Hwa;
Dikoglu, Esra;
Campos-Xavier, Belinda;
Girardi, Enrico;
Superti-Furga, Giulio;
Bonafé, Luisa;
Rivolta, Carlo;
Unger, Sheila;
Superti-Furga, Andrea

Publication type:

Article

Indel variant analysis of short-read sequencing data with Scalpel.

Published in:

Nature Protocols, 2016, v. 11, n. 12, p. 2529, doi. 10.1038/nprot.2016.150

By:

Fang, Han;
Bergmann, Ewa A;
Arora, Kanika;
Vacic, Vladimir;
Zody, Michael C;
Iossifov, Ivan;
O'Rawe, Jason A;
Wu, Yiyang;
Jimenez Barron, Laura T;
Rosenbaum, Julie;
Ronemus, Michael;
Lee, Yoon-ha;
Wang, Zihua;
Dikoglu, Esra;
Jobanputra, Vaidehi;
Lyon, Gholson J;
Wigler, Michael;
Schatz, Michael C;
Narzisi, Giuseppe

Publication type:

Article

Evidence of SARS-CoV-2-Specific T-Cell-Mediated Myocarditis in a MIS-A Case.

Published in:

Frontiers in Immunology, 2021, v. 12, p. 1, doi. 10.3389/fimmu.2021.779026

By:

Vannella, Kevin M.;
Oguz, Cihan;
Stein, Sydney R.;
Pittaluga, Stefania;
Dikoglu, Esra;
Kanwal, Arjun;
Ramelli, Sabrina C.;
Briese, Thomas;
Su, Ling;
Wu, Xiaolin;
Ramos-Benitez, Marcos J.;
Perez-Valencia, Luis J.;
Babyak, Ashley;
Cha, Nu Ri;
Chung, Joon-Yong;
Ylaya, Kris;
Madathil, Ronson J.;
Saharia, Kapil K.;
Scalea, Thomas M.;
Tran, Quincy K.

Publication type:

Article