1. 12th International CHARGE syndrome conference proceedings. Issue 4 (11th January 2016) Authors: Martin, Donna M.; Salem‐Hartshorne, Nancy; Hartshorne, Timothy S.; Scacheri, Peter C.; Hefner, Margaret A. Journal: American journal of medical genetics Issue: Volume 170:Issue 4(2016) Page Start: 856 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Age‐related effect of serotonin transporter genotype on amygdala and prefrontal cortex function in adolescence. Issue 2 (5th November 2012) Authors: Wiggins, Jillian Lee; Bedoyan, Jirair K.; Carrasco, Melisa; Swartz, Johnna R.; Martin, Donna M.; Monk, Christopher S. Journal: Human brain mapping Issue: Volume 35:Issue 2(2014:Feb.) Page Start: 646 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Atypical phenotypes associated with pathogenic CHD7 variants and a proposal for broadening CHARGE syndrome clinical diagnostic criteria. Issue 2 (21st November 2015) Authors: Hale, Caitlin L.; Niederriter, Adrienne N.; Green, Glenn E.; Martin, Donna M. Journal: American journal of medical genetics Issue: Volume 170:Issue 2(2016) Page Start: 344 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Axial level‐specific regulation of neuronal development: Lessons from PITX2. Issue 2 (14th August 2014) Authors: Waite, Mindy R.; Martin, Donna M. Journal: Journal of neuroscience research Issue: Volume 93:Issue 2(2015) Page Start: 195 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Chromatin remodeler Chd7 regulates photoreceptor development and outer segment length. (January 2023) Authors: Krueger, Laura A.; Bills, Jessica D.; Lim, Zun Yi; Skidmore, Jennifer M.; Martin, Donna M.; Morris, Ann C. Journal: Experimental eye research Issue: Volume 226(2023) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Congenital heart defects in CHARGE: The molecular role of CHD7 and effects on cardiac phenotype and clinical outcomes. Issue 1 (13th December 2019) Authors: Meisner, Joshua K.; Martin, Donna M. Other Names: Kruszka Paul guestEditor.; Beaton Andrea guestEditor. Journal: American journal of medical genetics Issue: Volume 184:Issue 1(2020) Page Start: 81 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Duplication 2p25 in a child with clinical features of CHARGE syndrome. Issue 5 (6th February 2016) Authors: Sperry, Ethan D.; Schuette, Jane L.; van Ravenswaaij‐Arts, Conny M. A.; Green, Glenn E.; Martin, Donna M. Journal: American journal of medical genetics Issue: Volume 170:Issue 5(2016) Page Start: 1148 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Erratum to "The influence of 5-HTTLPR transporter genotype on amygdala-subgenual anterior cingulate cortex connectivity in autism spectrum disorder" [Dev. Cognit. Neurosci. 24 April (2017) 12–20]. (October 2020) Authors: Velasquez, Francisco; Wiggins, Jillian Lee; Mattson, Whitney I.; Martin, Donna M.; Lord, Catherine; Monk, Christopher S. Journal: Developmental cognitive neuroscience Issue: Volume 45(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Genotype–phenotype correlations in individuals with pathogenic RERE variants. Issue 5 (25th January 2018) Authors: Jordan, Valerie K.; Fregeau, Brieana; Ge, Xiaoyan; Giordano, Jessica; Wapner, Ronald J.; Balci, Tugce B.; Carter, Melissa T.; Bernat, John A.; Moccia, Amanda N.; Srivastava, Anshika; Martin, Donna M.; Bielas, Stephanie L.; Pappas, John; Svoboda, Melissa D.; Rio, Marlène; Boddaert, Nathalie; Canta... Journal: Human mutation Issue: Volume 39:Issue 5(2018) Page Start: 666 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Incorporation of exome‐based CNV analysis makes trio‐WES a more powerful tool for clinical diagnosis in neurodevelopmental disorders: A retrospective study. Issue 8 (31st May 2021) Authors: Zhai, Yiwen; Zhang, Zhanhui; Shi, Panlai; Martin, Donna M.; Kong, Xiangdong Journal: Human mutation Issue: Volume 42:Issue 8(2021) Page Start: 990 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗