1. A compound T60A and V122I heterozygosity in the transthyretin gene causing early onset severe cardiac amyloidosis. (June 2014) Authors: Liu, Yi-Chang; Reddi, Honey Vodur; Waheed, Sarah; Alapat, Daisy; Highsmith, W. Edward; Edmondson, Ricky D.; Barlogie, Bart; van Rhee, Frits Journal: Amyloid Issue: Volume 21:Number 2(2014:Jun.) Page Start: 134 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Cervicomedullary compression as the main manifestation of wild-type transthyretin amyloidosis. (3rd April 2017) Authors: Rezania, Kourosh; Pytel, Peter; Highsmith, W. Edward; Gabikian, Patrik Journal: Amyloid Issue: Volume 24:Number 2(2017) Page Start: 133 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Complex p.T88N/W130R mutation in the lysozyme gene leading to hereditary lysozyme amyloidosis with biopsy-proven cardiac involvement. (2nd January 2017) Authors: Sperry, Brett W.; Dispenzieri, Angela; Ikram, Asad; Grogan, Martha; Theis, Jason D.; Leung, Nelson; Highsmith, W. Edward; Maleszewski, Joseph J.; Hanna, Mazen Journal: Amyloid Issue: Volume 24:Number 1(2017) Page Start: 60 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. False Negative Cell-Free DNA Screening Result in a Newborn with Trisomy 13. (22nd February 2016) Authors: Cao, Yang; Hoppman, Nicole L.; Kerr, Sarah E.; Sattler, Christopher A.; Borowski, Kristi S.; Wick, Myra J.; Highsmith, W. Edward; Aypar, Umut Other Names: Morrison Patrick Academic Editor. Journal: Case reports in genetics Issue: Volume 2016(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Mismatch Cleavage Detects Base Deletion in Cystic Fibrosis Gene. (October 1998) Authors: Hsu, Ih-Chang; Highsmith, W. Edward; Xu, Jingfan; Kong, Dehe Journal: Biotechniques Issue: Volume 25:Number 4(1998) Page Start: 692 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Mitochondrial DNA sequence data reveals association of haplogroup U with psychosis in bipolar disorder. (January 2017) Authors: Frye, Mark A.; Ryu, Euijung; Nassan, Malik; Jenkins, Gregory D.; Andreazza, Ana C.; Evans, Jared M.; McElroy, Susan L.; Oglesbee, Devin; Highsmith, W. Edward; Biernacka, Joanna M. Journal: Journal of psychiatric research Issue: Volume 84(2017) Page Start: 221 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Neurodevelopmental Disabilities in Children With Intermediate and Premutation Range Fragile X Cytosine-Guanine-Guanine Expansions. (March 2014) Authors: Renda, Meredith M.; Voigt, Robert G.; Babovic-Vuksanovic, Dusica; Highsmith, W. Edward; Vinson, Sherry S.; Sadowski, Christine M.; Hagerman, Randi J. Journal: Journal of child neurology Issue: Volume 29:Number 3(2014:Mar.) Page Start: 326 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Systemic transthyretin amyloidosis in a patient with bent spine syndrome. (2nd May 2013) Authors: Rezania, Kourosh; Pytel, Peter; Smit, Laurel J.; Mastrianni, James; Dina, Michelle A.; Highsmith, W. Edward; Dogan, Ahmet Journal: Amyloid Issue: Volume 20:Number 2(2013:Jun.) Page Start: 131 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗