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Works by Middlebrooks, Candace D.

Results: 6

1

Myopia in Chinese families shows linkage to 10q26.13.

Published in:

Molecular Vision, 2018, v. 24, p. 29

By:

Musolf, Anthony M.;
Simpson, Claire L.;
Long, Kyle A.;
Moiz, Bilal A.;
Lewis, Deyana D.;
Middlebrooks, Candace D.;
Portas, Laura;
Murgia, Federico;
Ciner, Elise B.;
Bailey-Wilson, Joan E.;
Stambolian, Dwight

Publication type:

Article

2

An Examination of the Relationship between Hotspots and Recombination Associated with Chromosome 21 Nondisjunction.

Published in:

PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0099560

By:

Oliver, Tiffany Renee;
Middlebrooks, Candace D.;
Tinker, Stuart W.;
Allen, Emily Graves;
Bean, Lora J. H.;
Begum, Ferdouse;
Feingold, Eleanor;
Chowdhury, Reshmi;
Cheung, Vivian;
Sherman, Stephanie L.

Publication type:

Article

3

Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12881-019-0752-8

By:

Simpson, Claire L.;
Musolf, Anthony M.;
Li, Qing;
Portas, Laura;
Murgia, Federico;
Cordero, Roberto Y.;
Cordero, Jennifer B.;
Moiz, Bilal A.;
Holzinger, Emily R.;
Middlebrooks, Candace D.;
Lewis, Deyana D.;
Bailey-Wilson, Joan E.;
Stambolian, Dwight

Publication type:

Article

4

Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 6, p. 1203, doi. 10.1093/hmg/ddv492

By:

Figueroa, Jonine D.;
Middlebrooks, Candace D.;
Rouf Banday, A.;
Ye, Yuanqing;
Garcia-Closas, Montserrat;
Chatterjee, Nilanjan;
Koutros, Stella;
Kiemeney, Lambertus A.;
Rafnar, Thorunn;
Bishop, Timothy;
Furberg, Helena;
Matullo, Giuseppe;
Golka, Klaus;
Gago-Dominguez, Manuela;
Taylor, Jack A.;
Fletcher, Tony;
Siddiq, Afshan;
Cortessis, Victoria K.;
Kooperberg, Charles;
Cussenot, Olivier

Publication type:

Article

5

Genome-wide association study identified SNP on 15q24 associated with bladder cancer risk in Japanese population.

Published in:

Human Molecular Genetics, 2015, v. 24, n. 4, p. 1177, doi. 10.1093/hmg/ddu512

By:

Koichi Matsuda;
Atsushi Takahashi;
Middlebrooks, Candace D.;
Wataru Obara;
Yasutomo Nasu;
Keiji Inoue;
Kenji Tamura;
Ichiro Yamasaki;
Yoshio Naya;
Chizu Tanikawa;
Ri Cui;
Figueroa, Jonine D.;
Silverman, Debra T.;
Rothman, Nathaniel;
Mikio Namiki;
Yoshihiko Tomita;
Hiroyuki Nishiyama;
Kenjiro Kohri;
Takashi Deguchi;
Masayuki Nakagawa

Publication type:

Article

6

Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21.

Published in:

Human Molecular Genetics, 2014, v. 23, n. 2, p. 408, doi. 10.1093/hmg/ddt433

By:

Middlebrooks, Candace D.;
Mukhopadhyay, Nandita;
Tinker, Stuart W.;
Allen, Emily Graves;
Bean, Lora J. H.;
Begum, Ferdouse;
Chowdhury, Reshmi;
Cheung, Vivian;
Doheny, Kimberly;
Adams, Marcia;
Feingold, Eleanor;
Sherman, Stephanie L.

Publication type:

Article