11. Cover Image, Volume 39, Issue 11. Issue 11 (11th October 2018) Authors: Zastrow, Diane B.; Baudet, Heather; Shen, Wei; Thomas, Amanda; Si, Yue; Weaver, Meredith A.; Lager, Angela M.; Liu, Jixia; Mangels, Rachel; Dwight, Selina S.; Wright, Matt W.; Dobrowolski, Steven F.; Eilbeck, Karen; Enns, Gregory M.; Feigenbaum, Annette; Lichter‐Konecki, Uta; Lyon, Elaine; Pasqua... Other Names: Rehm Heidi L. guestEditor.; Berg Jonathan S. guestEditor.; Plon Sharon E. guestEditor. Journal: Human mutation Issue: Volume 39:Issue 11(2018) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
12. Evidence‐based assessments of clinical actionability in the context of secondary findings: Updates from ClinGen's Actionability Working Group. Issue 11 (11th October 2018) Authors: Webber, Elizabeth M.; Hunter, Jessica Ezzell; Biesecker, Leslie G.; Buchanan, Adam H.; Clarke, Elizabeth V.; Currey, Erin; Dagan‐Rosenfeld, Orit; Lee, Kristy; Lindor, Noralane M.; Martin, Christa Lese; Milosavljevic, Aleksandar; Mittendorf, Kathleen F.; Muessig, Kristin R.; O'Daniel, Julianne M.;... Other Names: Rehm Heidi L. guestEditor.; Berg Jonathan S. guestEditor.; Plon Sharon E. guestEditor. Journal: Human mutation Issue: Volume 39:Issue 11(2018) Page Start: 1677 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
13. Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing loss. Issue 11 (11th October 2018) Authors: Oza, Andrea M.; DiStefano, Marina T.; Hemphill, Sarah E.; Cushman, Brandon J.; Grant, Andrew R.; Siegert, Rebecca K.; Shen, Jun; Chapin, Alex; Boczek, Nicole J.; Schimmenti, Lisa A.; Murry, Jaclyn B.; Hasadsri, Linda; Nara, Kiyomitsu; Kenna, Margaret; Booth, Kevin T.; Azaiez, Hela; Griffith, Andr... Other Names: Rehm Heidi L. guestEditor.; Berg Jonathan S. guestEditor.; Plon Sharon E. guestEditor. Journal: Human mutation Issue: Volume 39:Issue 11(2018) Page Start: 1593 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
14. Genetic database software as medical devices. Issue 11 (11th October 2018) Authors: Thorogood, Adrian; Touré, Seydina B.; Ordish, Johan; Hall, Alison; Knoppers, Bartha Other Names: Rehm Heidi L. guestEditor.; Berg Jonathan S. guestEditor.; Plon Sharon E. guestEditor. Journal: Human mutation Issue: Volume 39:Issue 11(2018) Page Start: 1702 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
15. Gene‐specific criteria for PTEN variant curation: Recommendations from the ClinGen PTEN Expert Panel. Issue 11 (11th October 2018) Authors: Mester, Jessica L.; Ghosh, Rajarshi; Pesaran, Tina; Huether, Robert; Karam, Rachid; Hruska, Kathleen S.; Costa, Helio A.; Lachlan, Katherine; Ngeow, Joanne; Barnholtz‐Sloan, Jill; Sesock, Kaitlin; Hernandez, Felicia; Zhang, Liying; Milko, Laura; Plon, Sharon E.; Hegde, Madhuri; Eng, Charis Other Names: Rehm Heidi L. guestEditor.; Berg Jonathan S. guestEditor.; Plon Sharon E. guestEditor. Journal: Human mutation Issue: Volume 39:Issue 11(2018) Page Start: 1581 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
16. Integrating somatic variant data and biomarkers for germline variant classification in cancer predisposition genes. Issue 11 (11th October 2018) Authors: Walsh, Michael F.; Ritter, Deborah I.; Kesserwan, Chimene; Sonkin, Dmitriy; Chakravarty, Debyani; Chao, Elizabeth; Ghosh, Rajarshi; Kemel, Yelena; Wu, Gang; Lee, Kristy; Kulkarni, Shashikant; Hedges, Dale; Mandelker, Diana; Ceyhan‐Birsoy, Ozge; Luo, Minjie; Drazer, Michael; Zhang, Liying; Offit, ... Other Names: Rehm Heidi L. guestEditor.; Berg Jonathan S. guestEditor.; Plon Sharon E. guestEditor. Journal: Human mutation Issue: Volume 39:Issue 11(2018) Page Start: 1542 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
17. Issue Information. Issue 11 (11th October 2018) Other Names: Rehm Heidi L. guestEditor.; Berg Jonathan S. guestEditor.; Plon Sharon E. guestEditor. Journal: Human mutation Issue: Volume 39:Issue 11(2018) Page Start: 1469 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
18. On the verge of diagnosis: Detection, reporting, and investigation of de novo variants in novel genes identified by clinical sequencing. Issue 11 (11th October 2018) Authors: Thiffault, Isabelle; Cadieux‐Dion, Maxime; Farrow, Emily; Caylor, Raymond; Miller, Neil; Soden, Sarah; Saunders, Carol Other Names: Rehm Heidi L. guestEditor.; Berg Jonathan S. guestEditor.; Plon Sharon E. guestEditor. Journal: Human mutation Issue: Volume 39:Issue 11(2018) Page Start: 1505 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
19. Quantifying the potential of functional evidence to reclassify variants of uncertain significance in the categorical and Bayesian interpretation frameworks. Issue 11 (5th September 2018) Authors: Brnich, Sarah E.; Rivera‐Muñoz, Edgar A.; Berg, Jonathan S. Other Names: Rehm Heidi L. guestEditor.; Berg Jonathan S. guestEditor.; Plon Sharon E. guestEditor. Journal: Human mutation Issue: Volume 39:Issue 11(2018) Page Start: 1531 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
20. Recommendations for interpreting the loss of function PVS1 ACMG/AMP variant criterion. Issue 11 (7th September 2018) Authors: Abou Tayoun, Ahmad N.; Pesaran, Tina; DiStefano, Marina T.; Oza, Andrea; Rehm, Heidi L.; Biesecker, Leslie G.; Harrison, Steven M. Other Names: Rehm Heidi L. guestEditor.; Berg Jonathan S. guestEditor.; Plon Sharon E. guestEditor. Journal: Human mutation Issue: Volume 39:Issue 11(2018) Page Start: 1517 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗