1. A case of primary cutaneous Ewing sarcoma in a neutropenic patient. (16th January 2019) Authors: Brown‐Joel, Zoe O.; Bellizzi, Andrew M.; Darbro, Benjamin W.; Snow, Anthony N.; Tanas, Munir R.; Keeney, Matthew E.; Stone, Mary S.; Wanat, Karolyn A.; Roth, Gretchen M. Journal: Journal of cutaneous pathology Issue: Volume 46:Number 3(2019) Page Start: 238 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel porcine model of ataxia telangiectasia reproduces neurological features and motor deficits of human disease. (15th September 2015) Authors: Beraldi, Rosanna; Chan, Chun-Hung; Rogers, Christopher S.; Kovács, Attila D.; Meyerholz, David K.; Trantzas, Constantin; Lambertz, Allyn M.; Darbro, Benjamin W.; Weber, Krystal L.; White, Katherine A.M.; Rheeden, Richard V.; Kruer, Michael C.; Dacken, Brian A.; Wang, Xiao-Jun; Davis, Bryan T.; Ro... Journal: Human molecular genetics Issue: Volume 24:Number 22(2015:Nov. 15) Page Start: 6473 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Assessment of nociception and related quality-of-life measures in a porcine model of neurofibromatosis type 1. Issue 11 (November 2019) Authors: Khanna, Rajesh; Moutal, Aubin; White, Katherine A.; Chefdeville, Aude; Negrao de Assis, Pedro; Cai, Song; Swier, Vicki J.; Bellampalli, Shreya S.; Giunta, Marissa D.; Darbro, Benjamin W.; Quelle, Dawn E.; Sieren, Jessica C.; Wallace, Margaret R.; Rogers, Christopher S.; Meyerholz, David K.; Weime... Journal: Pain Issue: Volume 160:Issue 11(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Candidate modifier genes for immune function in 22q11.2 deletion syndrome. Issue 1 (12th December 2019) Authors: Pinnaro, Catherina T.; Henry, Travis; Major, Heather J.; Parida, Mrutyunjaya; DesJardin, Lucy E.; Manak, John R.; Darbro, Benjamin W. Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 1(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Development of Secondary Acute Myeloid Leukemia in a Pediatric Patient Concurrently Receiving Primary Therapy for Ewing Sarcoma. Issue 7 (October 2017) Authors: McNew, Brandon R.; Darbro, Benjamin W.; Ma, Deqin; Gordon, David J. Journal: Journal of pediatric hematology/oncology Issue: Volume 39:Issue 7(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Evaluating Familial Essential Tremor with Novel Genetic Approaches: Is it a Genotyping or Phenotyping Issue?. (20th October 2014) Authors: Gonzalez-Alegre, Pedro; Di Paola, Jorge; Wang, Kai; Fabbro, Shay; Yu, Hung-Chun; Shaikh, Tamim H.; Darbro, Benjamin W.; Bassuk, Alexander G. Editors: Louis, Elan D. Journal: Tremor and other hyperkinetic movements Issue: Volume 4(2014) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Expanding the genotypic and phenotypic spectrum of severe serine biosynthesis disorders. Issue 9 (15th July 2020) Authors: Abdelfattah, Fatima; Kariminejad, Ariana; Kahlert, Anne‐Karin; Morrison, Patrick J.; Gumus, Evren; Mathews, Katherine D.; Darbro, Benjamin W.; Amor, David J.; Walsh, Maie; Sznajer, Yves; Weiß, Luisa; Weidensee, Sabine; Chitayat, David; Shannon, Patrick; Bermejo‐Sánchez, Eva; Riaño‐Galán, Isolina;... Journal: Human mutation Issue: Volume 41:Issue 9(2020) Page Start: 1615 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Immunohistochemical Markers for Prospective Studies in Neurofibromatosis-1 Porcine Models. (October 2017) Authors: Meyerholz, David K.; Ofori-Amanfo, Georgina K.; Leidinger, Mariah R.; Goeken, J. Adam; Khanna, Rajesh; Sieren, Jessica C.; Darbro, Benjamin W.; Quelle, Dawn E.; Weimer, Jill M. Journal: Journal of histochemistry and cytochemistry Issue: Volume 65:Number 10(2017:Oct.) Page Start: 607 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. In trans variant calling reveals enrichment for compound heterozygous variants in genes involved in neuronal development and growth. (13th June 2019) Authors: Cox, Allison J.; Grady, Fillan; Velez, Gabriel; Mahajan, Vinit B.; Ferguson, Polly J.; Kitchen, Andrew; Darbro, Benjamin W.; Bassuk, Alexander G. Journal: Genetical research Issue: Volume 101(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Intron mutations and early transcription termination in Duchenne and Becker muscular dystrophy. Issue 4 (7th March 2022) Authors: Waldrop, Megan A.; Moore, Steven A.; Mathews, Katherine D.; Darbro, Benjamin W.; Medne, Livja; Finkel, Richard; Connolly, Anne M.; Crawford, Thomas O.; Drachman, Daniel; Wein, Nicolas; Habib, Ali A.; Krzesniak‐Swinarska, Monika A.; Zaidman, Craig M.; Collins, James J.; Jokela, Manu; Udd, Bjarne; ... Journal: Human mutation Issue: Volume 43:Issue 4(2022) Page Start: 511 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗