1. A rapid gene sequencing panel strategy to facilitate precision neonatal medicine. Issue 7 (12th May 2017) Authors: Brunelli, Luca; Mao, Rong; Jenkins, Sabrina Malone; Bleyl, Steven B.; Dames, Shale A.; Miller, Christine E.; Ostrander, Betsy; Tvrdik, Tatiana; Andrews, Seth; Flores, Josue; Patel, Shrena; Gudgeon, James M.; Schaefer, Susan Journal: American journal of medical genetics Issue: Volume 173:Issue 7(2017) Page Start: 1979 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A virtual community health field project during the COVID‐19 pandemic. (23rd November 2020) Authors: Miller, Christine E.; Benton, Kim; Iyer, Parvati; Jue, Bonnie Journal: Journal of dental education Issue: Volume 85(2021)Supplement 1 Page Start: 958 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Assessing clinical education tools for expanded carrier screening. Issue 2 (1st November 2020) Authors: Dugger, Chloe; Anderson, Hannah S.; Miller, Christine E.; Wong, Bob; Johnson, Erin P.; Rothwell, Erin Journal: Journal of genetic counseling Issue: Volume 30:Issue 2(2021) Page Start: 606 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Comprehensive variant calling from whole‐genome sequencing identifies a complex inversion that disrupts ZFPM2 in familial congenital diaphragmatic hernia. Issue 4 (4th February 2022) Authors: Nicholas, Thomas J.; Al‐Sweel, Najla; Farrell, Andrew; Mao, Rong; Bayrak‐Toydemir, Pinar; Miller, Christine E.; Bentley, Dawn; Palmquist, Rachel; Moore, Barry; Hernandez, Edgar J.; Cormier, Michael J.; Fredrickson, Eric; Noble, Katherine; Rynearson, Shawn; Holt, Carson; Karren, Mary Anne; Bo... Journal: Molecular genetics & genomic medicine Issue: Volume 10:Issue 4(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Genetic counselor review of genetic test orders in a reference laboratory reduces unnecessary testing. Issue 5 (24th March 2014) Authors: Miller, Christine E.; Krautscheid, Patti; Baldwin, Erin E.; Tvrdik, Tatiana; Openshaw, Amanda S.; Hart, Kim; LaGrave, Danielle Journal: American journal of medical genetics Issue: Volume 164:Issue 5(2014.) Page Start: 1094 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Multiple endocrine neoplasia type 2 (MEN2) and RET specific modifications of the ACMG/AMP variant classification guidelines and impact on the MEN2 RET database. Issue 12 (31st October 2022) Authors: Margraf, Rebecca L.; Alexander, Rachel Z.; Fulmer, Makenzie L.; Miller, Christine E.; Coupal, Elena; Mao, Rong Journal: Human mutation Issue: Volume 43:Issue 12(2022) Page Start: 1780 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Novel mutation in CCBE 1 as a cause of recurrent hydrops fetalis from Hennekam lymphangiectasia‐lymphedema syndrome‐1. Issue 12 (24th October 2018) Authors: Melber, Dora J.; Andreasen, Tara S.; Mao, Rong; Tvrdik, Tatiana; Miller, Christine E.; Moore, Thomas R.; Woelkers, Douglas A.; Lamale‐Smith, Leah M. Journal: Clinical case reports Issue: Volume 6:Issue 12(2018) Page Start: 2358 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Targeted gene panel sequencing for the rapid diagnosis of acutely ill infants. Issue 7 (13th June 2019) Authors: Brunelli, Luca; Jenkins, Sabrina M.; Gudgeon, James M.; Bleyl, Steven B.; Miller, Christine E.; Tvrdik, Tatiana; Dames, Shale A.; Ostrander, Betsy; Daboub, Josue A. F.; Zielinski, Brandon A.; Zinkhan, Erin K.; Underhill, Hunter R.; Wilson, Theodore; Bonkowsky, Joshua L.; Yost, Christian C.; Botto... Journal: Molecular genetics & genomic medicine Issue: Volume 7:Issue 7(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗