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Author/Creator Scheetz, Todd E.

2. A targeted sequencing study of glutamatergic candidate genes in suicide attempters with bipolar disorder. Issue 8 (2nd August 2016)

Authors:
Gaynor, Sophia C.; Breen, Marie E.; Monson, Eric T.; de Klerk, Kelly; Parsons, Meredith; DeLuca, Adam P.; Scheetz, Todd E.; Zandi, Peter P.; Potash, James B.; Willour, Virginia L.
Journal:
American journal of medical genetics
Issue:
Volume 171:Issue 8(2016)
Page Start:
1080
Record Type:
Journal Article
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4. AudioGene: Predicting Hearing Loss Genotypes from Phenotypes to Guide Genetic Screening. Issue 4 (19th February 2013)

Authors:
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.
Journal:
Human mutation
Issue:
Volume 34:Issue 4(2013:Apr.)
Page Start:
539
Record Type:
Journal Article
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5. Audioprofile Surfaces: The 21st Century Audiogram. (May 2016)

Authors:
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...
Journal:
Annals of otology, rhinology & laryngology
Issue:
Volume 125:Number 5(2016:May)
Page Start:
361
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

6. AUTOIMMUNE RETINOPATHY MIMICKING HERITABLE RETINAL DEGENERATION IN A PATIENT WITH COMMON VARIABLE IMMUNE DEFICIENCY. Issue Volume 16:Issues 1(2022) (21st November 2019)

Authors:
Wiley, Luke A.; Binkley, Elaine M.; DeLuca, Adam P.; Workalemahu, Grefachew; Tatro, Nicole J.; Luse, Meagan A.; Kennedy, Elizabeth L.; Folk, James C.; Scheetz, Todd E.; Ballas, Zuhair K.; Tucker, Budd A.; Mullins, Robert F.; Han, Ian C.; Stone, Edwin M.
Journal:
Retinal cases & brief reports
Issue:
Volume 16:Issues 1(2022)
Page Start:
111
Record Type:
Journal Article
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7. AUTOIMMUNE RETINOPATHY MIMICKING HERITABLE RETINAL DEGENERATION IN A PATIENT WITH COMMON VARIABLE IMMUNE DEFICIENCY. Issue Volume 16:Issues 1(2022) (January 2022)

Authors:
Wiley, Luke A.; Binkley, Elaine M.; DeLuca, Adam P.; Workalemahu, Grefachew; Tatro, Nicole J.; Luse, Meagan A.; Kennedy, Elizabeth L.; Folk, James C.; Scheetz, Todd E.; Ballas, Zuhair K.; Tucker, Budd A.; Mullins, Robert F.; Han, Ian C.; Stone, Edwin M.
Journal:
Retinal cases & brief reports
Issue:
Volume 16:Issues 1(2022)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

10. Heterozygous Triplication of Upstream Regulatory Sequences Leads to Dysregulation of Matrix Metalloproteinase 19 in Patients with Cavitary Optic Disc Anomaly. Issue 3 (13th March 2015)

Authors:
Hazlewood, Ralph J.; Roos, Benjamin R.; Solivan‐Timpe, Frances; Honkanen, Robert A.; Jampol, Lee M.; Gieser, Stephen C.; Meyer, Kacie J.; Mullins, Robert F.; Kuehn, Markus H.; Scheetz, Todd E.; Kwon, Young H.; Alward, Wallace L.M.; Stone, Edwin M.; Fingert, John H.
Journal:
Human mutation
Issue:
Volume 36:Issue 3(2015:Mar.)
Page Start:
369
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗