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Mine water stewardship in Arizona.
Published in:
Mining Engineering, 2023, v. 75, n. 7, p. 16
By:
- Braun, Terry
Publication type:
Article
Correction to: Genomics of NSCLC patients both affirm PD-L1 expression and predict their clinical responses to anti-PD-1 immunotherapy.
Published in:
2018
By:
- Brogden, Kim A.;
- Parashar, Deepak;
- Hallier, Andrea R.;
- Braun, Terry;
- Qian, Fang;
- Rizvi, Naiyer A.;
- Bossler, Aaron D.;
- Milhem, Mohammed M.;
- Chan, Timothy A.;
- Abbasi, Taher;
- Vali, Shireen
Publication type:
journal article
Genomics of NSCLC patients both affirm PD-L1 expression and predict their clinical responses to anti-PD-1 immunotherapy.
Published in:
2018
By:
- Brogden, Kim A;
- Parashar, Deepak;
- Hallier, Andrea R;
- Braun, Terry;
- Qian, Fang;
- Rizvi, Naiyer A;
- Bossler, Aaron D;
- Milhem, Mohammed M;
- Chan, Timothy A;
- Abbasi, Taher;
- Vali, Shireen
Publication type:
journal article
Assessing variants of uncertain significance implicated in hearing loss using a comprehensive deafness proteome.
Published in:
Human Genetics, 2023, v. 142, n. 6, p. 819, doi. 10.1007/s00439-023-02559-9
By:
- Tollefson, Mallory R.;
- Gogal, Rose A.;
- Weaver, A. Monique;
- Schaefer, Amanda M.;
- Marini, Robert J.;
- Azaiez, Hela;
- Kolbe, Diana L.;
- Wang, Donghong;
- Weaver, Amy E.;
- Casavant, Thomas L.;
- Braun, Terry A.;
- Smith, Richard J. H.;
- Schnieders, Michael J.
Publication type:
Article
A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations.
Published in:
Human Genetics, 2020, v. 139, n. 10, p. 1315, doi. 10.1007/s00439-020-02174-y
By:
- Walls, W. Daniel;
- Moteki, Hideaki;
- Thomas, Taylor R.;
- Nishio, Shin-ya;
- Yoshimura, Hidekane;
- Iwasa, Yoichiro;
- Frees, Kathy L.;
- Nishimura, Carla J.;
- Azaiez, Hela;
- Booth, Kevin T.;
- Marini, Robert J.;
- Kolbe, Diana L.;
- Weaver, A. Monique;
- Schaefer, Amanda M.;
- Wang, Kai;
- Braun, Terry A.;
- Usami, Shin-ichi;
- Barr-Gillespie, Peter G.;
- Richardson, Guy P.;
- Smith, Richard J.
Publication type:
Article
Presacral neuroendocrine tumors associated with the Currarino syndrome.
Published in:
American Journal of Medical Genetics. Part A, 2021, v. 185, n. 5, p. 1582, doi. 10.1002/ajmg.a.62145
By:
- Scott, Aaron T.;
- Tessmann, Jonathon B.;
- Braun, Terry;
- Brown, Bartley;
- Breheny, Patrick J.;
- Darbro, Benjamin W.;
- Bellizzi, Andrew M.;
- Dillon, Joseph S.;
- O'Dorisio, Thomas M.;
- Alderson, Alice;
- Bennett, Bonita;
- Bernat, John A.;
- Metz, David C.;
- Howe, James R.
Publication type:
Article
Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome.
Published in:
Nature Genetics, 2002, v. 31, n. 4, p. 435, doi. 10.1038/ng935
By:
- Mykytyn, Kirk;
- Nishimura, Darryl Y.;
- Searby, Charles C.;
- Shastri, Mythreyi;
- Yen, Hsan-jan;
- Beck, John S.;
- Braun, Terry;
- Streb, Luan M.;
- Cornier, Alberto S.;
- Cox, Gerald F.;
- Fulton, Anne B.;
- Carmi, Rivka;
- Lüleci, Güven;
- Chandrasekharappa, Settara C.;
- Collins, Francis S.;
- Jacobson, Samuel G.;
- Heckenlively, John R.;
- Weleber, Richard G.;
- Stone, Edwin M.;
- Sheffield, Val C.
Publication type:
Article
Identification of the gene that, when mutated, causes the human obesity syndrome BBS4.
Published in:
Nature Genetics, 2001, v. 28, n. 2, p. 188, doi. 10.1038/88925
By:
- Mykytyn, Kirk;
- Braun, Terry;
- Carmi, Rivka;
- Haider, Neena B.;
- Searby, Charles C.;
- Shastri, Mythreyi;
- Beck, Gretel;
- Wright, Alan F.;
- Iannaccone, Alessandro;
- Elbedour, Khalil;
- Riise, Ruth;
- Baldi, Alfonso;
- Raas-Rothschild, Annick;
- Gorman, Susan W.;
- Duhl, David M.;
- Jacobson, Samuel G.;
- Casavant, Thomas;
- Stone, Edwin M.;
- Sheffield, Val C.
Publication type:
Article
A Genome-Wide Association Study for Primary Open Angle Glaucoma and Macular Degeneration Reveals Novel Loci.
Published in:
PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0058657
By:
- Scheetz, Todd E.;
- Fingert, John H.;
- Wang, Kai;
- Kuehn, Markus H.;
- Knudtson, Kevin L.;
- Alward, Wallace L. M.;
- Boldt, H. Culver;
- Russell, Stephen R.;
- Folk, James C.;
- Casavant, Thomas L.;
- Braun, Terry A.;
- Clark, Abbot F.;
- Stone, Edwin M.;
- Sheffield, Val C.
Publication type:
Article
Genome-wide analysis of copy number variants in age-related macular degeneration.
Published in:
Human Genetics, 2011, v. 129, n. 1, p. 91, doi. 10.1007/s00439-010-0904-6
By:
- Meyer, Kacie J.;
- Davis, Lea K.;
- Schindler, Emily I.;
- Beck, John S.;
- Rudd, Danielle S.;
- Grundstad, A. Jason;
- Scheetz, Todd E.;
- Braun, Terry A.;
- Fingert, John H.;
- Alward, Wallace L.;
- Kwon, Young H.;
- Folk, James C.;
- Russell, Stephen R.;
- Wassink, Thomas H.;
- Stone, Edwin M.;
- Sheffield, Val C.
Publication type:
Article
A novel, wearable, electronic visual aid to assist those with reduced peripheral vision.
Published in:
PLoS ONE, 2019, v. 14, n. 10, p. 1, doi. 10.1371/journal.pone.0223755
By:
- Brown, Ffion E.;
- Sutton, Janice;
- Yuen, Ho M.;
- Green, Dylan;
- Van Dorn, Spencer;
- Braun, Terry;
- Cree, Angela J.;
- Russell, Stephen R.;
- Lotery, Andrew J.
Publication type:
Article
Machine learning with the TCGA-HNSC dataset: improving usability by addressing inconsistency, sparsity, and high-dimensionality.
Published in:
BMC Bioinformatics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12859-019-2929-8
By:
- Rendleman, Michael C.;
- Buatti, John M.;
- Braun, Terry A.;
- Smith, Brian J.;
- Nwakama, Chibuzo;
- Beichel, Reinhard R.;
- Brown, Bart;
- Casavant, Thomas L.
Publication type:
Article
RABL6A inhibits tumor-suppressive PP2A/AKT signaling to drive pancreatic neuroendocrine tumor growth.
Published in:
2019
By:
- Umesalma, Shaikamjad;
- Kaemmer, Courtney A.;
- Kohlmeyer, Jordan L.;
- Letney, Blake;
- Schab, Angela M.;
- Reilly, Jacqueline A.;
- Sheehy, Ryan M.;
- Hagen, Jussara;
- Tiwari, Nitija;
- Fenghuang Zhan;
- Leidinger, Mariah R.;
- O'Dorisio, Thomas M.;
- Dillon, Joseph;
- Merrill, Ronald A.;
- Meyerholz, David K.;
- Perl, Abbey L.;
- Brown, Bart J.;
- Braun, Terry A.;
- Scott, Aaron T.;
- Ginader, Timothy
Publication type:
journal article
A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome.
Published in:
Clinical Genetics, 2022, v. 101, n. 3, p. 346, doi. 10.1111/cge.14105
By:
- Canpolat, Nur;
- Liu, Dingxiao;
- Atayar, Emine;
- Saygili, Seha;
- Kara, Nazli Sila;
- Westfall, Trudi A.;
- Ding, Qiong;
- Brown, Bartley J.;
- Braun, Terry A.;
- Slusarski, Diane;
- Karli Oguz, Kader;
- Ozluk, Yasemin;
- Tuysuz, Beyhan;
- Tastemel Ozturk, Tugba;
- Sever, Lale;
- Sezerman, Osman Ugur;
- Topaloglu, Rezan;
- Caliskan, Salim;
- Attanasio, Massimo;
- Ozaltin, Fatih
Publication type:
Article
Creation and validation of models to predict response to primary treatment in serous ovarian cancer.
Published in:
Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-85256-9
By:
- Gonzalez Bosquet, Jesus;
- Devor, Eric J.;
- Newtson, Andreea M.;
- Smith, Brian J.;
- Bender, David P.;
- Goodheart, Michael J.;
- McDonald, Megan E.;
- Braun, Terry A.;
- Thiel, Kristina W.;
- Leslie, Kimberly K.
Publication type:
Article
Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 25, p. 5136, doi. 10.1093/hmg/ddt367
By:
- Braun, Terry A.;
- Mullins, Robert F.;
- Wagner, Alex H.;
- Andorf, Jeaneen L.;
- Johnston, Rebecca M.;
- Bakall, Benjamin B.;
- Deluca, Adam P.;
- Fishman, Gerald A.;
- Lam, Byron L.;
- Weleber, Richard G.;
- Cideciyan, Artur V.;
- Jacobson, Samuel G.;
- Sheffield, Val C.;
- Tucker, Budd A.;
- Stone, Edwin M.
Publication type:
Article
A Comparison of Gene Expression Profiles between Glucocorticoid Responder and Non-Responder Bovine Trabecular Meshwork Cells Using RNA Sequencing.
Published in:
PLoS ONE, 2017, v. 12, n. 1, p. 1, doi. 10.1371/journal.pone.0169671
By:
- Bermudez, Jaclyn Y.;
- Webber, Hannah C.;
- Brown, Bartley;
- Braun, Terry A.;
- Clark, Abbot F.;
- Mao, Weiming
Publication type:
Article
Targeted Sequencing of FKBP5 in Suicide Attempters with Bipolar Disorder.
Published in:
PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0169158
By:
- Breen, Marie E.;
- Gaynor, Sophia C.;
- Monson, Eric T.;
- de Klerk, Kelly;
- Parsons, Meredith G.;
- Braun, Terry A.;
- DeLuca, Adam P.;
- Zandi, Peter P.;
- Potash, James B.;
- Willour, Virginia L.
Publication type:
Article
Audioprofile Surfaces.
Published in:
Annals of Otology, Rhinology & Laryngology, 2016, v. 125, n. 5, p. 361, doi. 10.1177/0003489415614863
By:
- Taylor, Kyle R.;
- Booth, Kevin T.;
- Azaiez, Hela;
- Sloan, Christina M.;
- Kolbe, Diana L.;
- Glanz, Emily N.;
- Shearer, A. Eliot;
- DeLuca, Adam P.;
- Anand, V. Nikhil;
- Hildebrand, Michael S.;
- Simpson, Allen C.;
- Eppsteiner, Robert W.;
- Scheetz, Todd E.;
- Braun, Terry A.;
- Huygen, Patrick L. M.;
- Smith, Richard J. H.;
- Casavant, Thomas L.
Publication type:
Article
Validation of computational prediction of horizontal gene transfer events-XenoCluster.
Published in:
Journal of Supercomputing, 2011, v. 57, n. 2, p. 141, doi. 10.1007/s11227-010-0386-2
By:
- Walters, Jesse D.;
- Bair, Thomas B.;
- Braun, Terry A.;
- Scheetz, Todd E.;
- Robinson, John P.;
- Casavant, Thomas L.
Publication type:
Article
Identifying Candidate Disease Genes with High-Performance Computing.
Published in:
Journal of Supercomputing, 2003, v. 26, n. 1, p. 7, doi. 10.1023/A:1024417200364
By:
- Braun, Terry A.;
- Scheetz, Todd E.;
- Webster, Gregg;
- Clark, Abe;
- Stone, Edwin M.;
- Sheffield, Val C.;
- Casavant, Thomas L.
Publication type:
Article
Optic nerve crush induces spatial and temporal gene expression patterns in retina and optic nerve of BALB/cJ mice.
Published in:
Molecular Neurodegeneration, 2014, v. 9, n. 1, p. 1, doi. 10.1186/1750-1326-9-14
By:
- Sharma, Tasneem P.;
- McDowell, Colleen M.;
- Yang Liu;
- Wagner, Alex H.;
- Thole, David;
- Faga, Benjamin P.;
- Wordinger, Robert J.;
- Braun, Terry A.;
- Clark, Abbot F.
Publication type:
Article
Progressive morphological changes and impaired retinal function associated with temporal regulation of gene expression after retinal ischemia/reperfusion injury in mice.
Published in:
Molecular Neurodegeneration, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1326-8-21
By:
- Byung-Jin Kim;
- Braun, Terry A.;
- Wordinger, Robert J.;
- Clark, Abbot F.
Publication type:
Article
Calpain-5 Mutations Cause Autoimmune Uveitis, Retinal Neovascularization, and Photoreceptor Degeneration.
Published in:
PLoS Genetics, 2012, v. 8, n. 10, p. 1, doi. 10.1371/journal.pgen.1003001
By:
- Mahajan, Vinit B.;
- Skeie, Jessica M.;
- Bassuk, Alexander G.;
- Fingert, John H.;
- Braun, Terry A.;
- Daggett, Heather T.;
- Folk, James C.;
- Sheffield, Val C.;
- Stone, Edwin M.
Publication type:
Article
Heterozygous Deep-Intronic Variants and Deletions in ABCA4 in Persons with Retinal Dystrophies and One Exonic ABCA4 Variant.
Published in:
Human Mutation, 2015, v. 36, n. 1, p. 43, doi. 10.1002/humu.22717
By:
- Bax, Nathalie M.;
- Sangermano, Riccardo;
- Roosing, Susanne;
- Thiadens, Alberta A.H.J.;
- Hoefsloot, Lies H.;
- den Born, L. Ingeborgh;
- Phan, Milan;
- Klevering, B. Jeroen;
- Westeneng‐van Haaften, Carla;
- Braun, Terry A.;
- Zonneveld‐Vrieling, Marijke N.;
- Wijs, Ilse;
- Mutlu, Merve;
- Stone, Edwin M.;
- den Hollander, Anneke I.;
- Klaver, Caroline C.W.;
- Hoyng, Carel B.;
- Cremers, Frans P.M.
Publication type:
Article
Prioritization of Retinal Disease Genes: An Integrative Approach.
Published in:
Human Mutation, 2013, v. 34, n. 6, p. 853, doi. 10.1002/humu.22317
By:
- Wagner, Alex H.;
- Taylor, Kyle R.;
- DeLuca, Adam P.;
- Casavant, Thomas L.;
- Mullins, Robert F.;
- Stone, Edwin M.;
- Scheetz, Todd E.;
- Braun, Terry A.
Publication type:
Article
Audio Gene: Predicting Hearing Loss Genotypes from Phenotypes to Guide Genetic Screening.
Published in:
Human Mutation, 2013, v. 34, n. 4, p. 539, doi. 10.1002/humu.22268
By:
- Taylor, Kyle R.;
- DeLuca, Adam P.;
- Shearer, A. Eliot;
- Hildebrand, Michael S.;
- Black‐Ziegelbein, E. Ann;
- Anand, V. Nikhil;
- Sloan, Christina M.;
- Eppsteiner, Robert W.;
- Scheetz, Todd E.;
- Huygen, Patrick L. M.;
- Smith, Richard J. H.;
- Braun, Terry A.;
- Casavant, Thomas L.
Publication type:
Article
DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.
Published in:
Human Mutation, 2011, v. 32, n. 7, p. 825, doi. 10.1002/humu.21512
By:
- Hildebrand, Michael S.;
- Morín, Matías;
- Meyer, Nicole C.;
- Mayo, Fernando;
- Modamio-Hoybjor, Silvia;
- Mencía, Angeles;
- Olavarrieta, Leticia;
- Morales-Angulo, Carmelo;
- Nishimura, Carla J.;
- Workman, Heather;
- DeLuca, Adam P.;
- del Castillo, Ignacio;
- Taylor, Kyle R.;
- Tompkins, Bruce;
- Goodman, Corey W.;
- Schrauwen, Isabelle;
- Wesemael, Maarten Van;
- Lachlan, K.;
- Shearer, A. Eliot;
- Braun, Terry A.
Publication type:
Article
Genome-wide identification of pseudogenes capable of disease-causing gene conversion.
Published in:
Human Mutation, 2006, v. 27, n. 6, p. 545, doi. 10.1002/humu.20335
By:
- Bischof, Jared M.;
- Chiang, Annie P.;
- Scheetz, Todd E.;
- Stone, Edwin M.;
- Casavant, Thomas L.;
- Sheffield, Val C.;
- Braun, Terry A.
Publication type:
Article
Prioritizing regions of candidate genes for efficient mutation screening.
Published in:
2006
By:
- Braun, Terry A.;
- Shankar, Suma P.;
- Davis, Steve;
- O'Leary, Brian;
- Scheetz, Todd E.;
- Clark, Abbot F.;
- Sheffield, Val C.;
- Casavant, Thomas L.;
- Stone, Edwin M.
Publication type:
Other
Functional Copy-Number Alterations as Diagnostic and Prognostic Biomarkers in Neuroendocrine Tumors.
Published in:
International Journal of Molecular Sciences, 2024, v. 25, n. 14, p. 7532, doi. 10.3390/ijms25147532
By:
- Vaughn, Hayley;
- Major, Heather;
- Kadera, Evangeline;
- Keck, Kendall;
- Dunham, Timothy;
- Qian, Qining;
- Brown, Bartley;
- Scott, Aaron;
- Bellizzi, Andrew M.;
- Braun, Terry;
- Breheny, Patrick;
- Quelle, Dawn E.;
- Howe, James R.;
- Darbro, Benjamin
Publication type:
Article
Prioritization of Fluorescence In Situ Hybridization (FISH) Probes for Differentiating Primary Sites of Neuroendocrine Tumors with Machine Learning.
Published in:
International Journal of Molecular Sciences, 2023, v. 24, n. 24, p. 17401, doi. 10.3390/ijms242417401
By:
- Pietan, Lucas;
- Vaughn, Hayley;
- Howe, James R.;
- Bellizzi, Andrew M.;
- Smith, Brian J.;
- Darbro, Benjamin;
- Braun, Terry;
- Casavant, Thomas
Publication type:
Article
TRANSCRIPT ANNOTATION PRIORITIZATION AND SCREENING SYSTEM (TrAPSS) FOR MUTATION SCREENING.
Published in:
Journal of Bioinformatics & Computational Biology, 2007, v. 5, n. 6, p. 1155, doi. 10.1142/S0219720007003132
By:
- O'LEARY, BRIAN M.;
- DAVIS, STEVEN G.;
- SMITH, MICHAEL F.;
- BROWN, BARTLEY;
- KEMP, MATHEW B.;
- ALMABRAZI, HAKEEM;
- GRUNDSTAD, JASON A.;
- BURNS, THOMAS;
- LEONTIEV, VLADIMIR;
- ANDORF, JEANEEN;
- CLARK, ABBOT F.;
- SHEFFIELD, VAL C.;
- CASAVANT, THOMAS L.;
- SCHEETZ, TODD E.;
- STONE, EDWIN M.;
- BRAUN, TERRY A.
Publication type:
Article
Cordova: Web-based management of genetic variation data.
Published in:
Bioinformatics, 2014, v. 30, n. 23, p. 3438, doi. 10.1093/bioinformatics/btu539
By:
- Ephraim, Sean S.;
- Anand, Nikhil;
- DeLuca, Adam P.;
- Taylor, Kyle R.;
- Kolbe, Diana L.;
- Simpson, Allen C.;
- Azaiez, Hela;
- Sloan, Christina M.;
- Shearer, A. Eliot;
- Hallier, Andrea R.;
- Casavant, Thomas L.;
- Scheetz, Todd E.;
- Smith, Richard J. H.;
- Braun, Terry A.
Publication type:
Article
Calculating the prevalence of cancer.
Published in:
Statistics in Medicine, 1992, v. 11, n. 12, p. 1579, doi. 10.1002/sim.4780111205
By:
- Coldman, Andrew J.;
- McBride, Mary L.;
- Braun, Terry
Publication type:
Article
Using the Phenome and Genome to Improve Genetic Diagnosis for Deafness.
Published in:
Otolaryngology-Head & Neck Surgery, 2012, v. 147, n. 5, p. 975, doi. 10.1177/0194599812454271
By:
- Eppsteiner, Robert W.;
- Shearer, A. Eliot;
- Hildebrand, Michael S.;
- Taylor, Kyle R.;
- DeLuca, Adam P.;
- Scherer, Steve;
- Huygen, Patrick;
- Scheetz, Todd E.;
- Braun, Terry A.;
- Casavant, Thomas L.;
- Smith, Richard J. H.
Publication type:
Article

Found: 36