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Differing Roles for TCF4 and COL8A2 in Central Corneal Thickness and Fuchs Endothelial Corneal Dystrophy.
Published in:
PLoS ONE, 2012, v. 7, n. 10, p. 1, doi. 10.1371/journal.pone.0046742
By:
- Igo Jr., Robert P.;
- Kopplin, Laura J.;
- Joseph, Peronne;
- Truitt, Barbara;
- Fondran, Jeremy;
- Bardenstein, David;
- Aldave, Anthony J.;
- Croasdale, Christopher R.;
- Price, Marianne O.;
- Rosenwasser, Miriam;
- Lass, Jonathan H.;
- Iyengar, Sudha K.
Publication type:
Article
Association between genes regulating neural pathways for quantitative traits of speech and language disorders.
Published in:
NPJ Genomic Medicine, 2021, v. 6, n. 1, p. 1, doi. 10.1038/s41525-021-00225-5
By:
- Benchek, Penelope;
- Igo, Robert P.;
- Voss-Hoynes, Heather;
- Wren, Yvonne;
- Miller, Gabrielle;
- Truitt, Barbara;
- Zhang, Wen;
- Osterman, Michael;
- Freebairn, Lisa;
- Tag, Jessica;
- Taylor, H. Gerry;
- Chan, E. Ricky;
- Roussos, Panos;
- Lewis, Barbara;
- Stein, Catherine M.;
- Iyengar, Sudha K.
Publication type:
Article
Variation in PTCHD2, CRISP3, NAP1L4, FSCB, and AP3B2 associated with spherical equivalent.
Published in:
Molecular Vision, 2016, v. 22, p. 1
By:
- Fei Chen;
- Duggal, Priya;
- Klein, Barbara E. K.;
- Lee, Kristine E.;
- Truitt, Barbara;
- Klein, Ronald;
- Iyengar, Sudha K.;
- Klein, Alison P.
Publication type:
Article
Importance of copy number variants in childhood apraxia of speech and other speech sound disorders.
Published in:
Communications Biology, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42003-024-06968-y
By:
- Chan, E. Ricky;
- Benchek, Penelope;
- Miller, Gabrielle;
- Brustoski, Kim;
- Schaffer, Ashleigh;
- Truitt, Barbara;
- Tag, Jessica;
- Freebairn, Lisa;
- Lewis, Barbara A.;
- Stein, Catherine M.;
- Iyengar, Sudha K.
Publication type:
Article
Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy.
Published in:
Nature Communications, 2017, v. 8, n. 3, p. 14898, doi. 10.1038/ncomms14898
By:
- Afshari, Natalie A.;
- Igo, Robert P.;
- Morris, Nathan J.;
- Stambolian, Dwight;
- Sharma, Shiwani;
- Pulagam, V. Lakshmi;
- Dunn, Steven;
- Stamler, John F.;
- Truitt, Barbara J.;
- Rimmler, Jacqueline;
- Kuot, Abraham;
- Croasdale, Christopher R.;
- Qin, Xuejun;
- Burdon, Kathryn P.;
- Riazuddin, S. Amer;
- Mills, Richard;
- Klebe, Sonja;
- Minear, Mollie A.;
- Zhao, Jiagang;
- Balajonda, Elmer
Publication type:
Article
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration.
Published in:
Human Molecular Genetics, 2014, v. 23, n. 21, p. 5827, doi. 10.1093/hmg/ddu276
By:
- Ratnapriya, Rinki;
- Zhan, Xiaowei;
- Fariss, Robert N.;
- Branham, Kari E.;
- Zipprer, David;
- Chakarova, Christina F.;
- Sergeev, Yuri V.;
- Campos, Maria M.;
- Othman, Mohammad;
- Friedman, James S.;
- Maminishkis, Arvydas;
- Waseem, Naushin H.;
- Brooks, Matthew;
- Rajasimha, Harsha K.;
- Edwards, Albert O.;
- Lotery, Andrew;
- Klein, Barbara E.;
- Truitt, Barbara J.;
- Li, Bingshan;
- Schaumberg, Debra A.
Publication type:
Article
Severe vascular calcification and tumoral calcinosis in a family with hyperphosphatemia: a fibroblast growth factor 23 mutation identified by exome sequencing.
Published in:
Nephrology Dialysis Transplantation, 2014, v. 29, n. 12, p. 2235, doi. 10.1093/ndt/gfu324
By:
- Shah, Anuja;
- Miller, Clinton J.;
- Nast, Cynthia C.;
- Adams, Mark D.;
- Truitt, Barbara;
- Tayek, John A.;
- Tong, Lili;
- Mehtani, Parag;
- Monteon, Francisco;
- Sedor, John R.;
- Clinkenbeard, Erica L.;
- White, Kenneth;
- Mehrotra, Rajnish;
- LaPage, Janine;
- Dickson, Patricia;
- Adler, Sharon G.;
- Iyengar, Sudha K.
Publication type:
Article

Found: 7

Differing Roles for TCF4 and COL8A2 in Central Corneal Thickness and Fuchs Endothelial Corneal Dystrophy.

Association between genes regulating neural pathways for quantitative traits of speech and language disorders.

Variation in PTCHD2, CRISP3, NAP1L4, FSCB, and AP3B2 associated with spherical equivalent.

Importance of copy number variants in childhood apraxia of speech and other speech sound disorders.

Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy.

Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration.

Severe vascular calcification and tumoral calcinosis in a family with hyperphosphatemia: a fibroblast growth factor 23 mutation identified by exome sequencing.