1. An exploratory trial implementing a community-based child oral health promotion intervention for Australian families from refugee and migrant backgrounds: a protocol paper for Teeth Tales. Issue 3 (12th March 2014) Authors: Gibbs, Lisa; Waters, Elizabeth; de Silva, Andrea; Riggs, Elisha; Moore, Laurence; Armit, Christine; Johnson, Britt; Morris, Michal; Calache, Hanny; Gussy, Mark; Young, Dana; Tadic, Maryanne; Christian, Bradley; Gondal, Iqbal; Watt, Richard; Pradel, Veronika; Truong, Mandy; Gold, Lisa Journal: BMJ open Issue: Volume 4:Issue 3(2014) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Cover, Volume 43, Issue 2. Issue 2 (28th January 2022) Authors: Sarafrazi, Soodabeh; Daugherty, Sean C.; Miller, Nicole; Boada, Patrick; Carpenter, Thomas O.; Chunn, Lauren; Dill, Kariena; Econs, Michael J.; Eisenbeis, Scott; Imel, Erik A.; Johnson, Britt; Kiel, Mark J.; Krolczyk, Stan; Ramesan, Prameela; Truty, Rebecca; Sabbagh, Yves Journal: Human mutation Issue: Volume 43:Issue 2(2022) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Diagnosing Lysosomal Storage Disorders: Fabry Disease. (1st April 2013) Authors: Bodamer, Olaf A.; Johnson, Britt; Dajnoki, Angela Editors: Haines, Jonathan L.; Korf, Bruce R.; Morton, Cynthia C.; Seidman, Christine E.; Seidman, J.G.; Smith, Douglas R. Journal: Current protocols in human genetics Issue: Volume 77(2013) Page Start: 17.13.1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Molecular Diagnoses of X‐Linked and Other Genetic Hypophosphatemias: Results From a Sponsored Genetic Testing Program. (10th November 2021) Authors: Rush, Eric T.; Johnson, Britt; Aradhya, Swaroop; Beltran, Daniel; Bristow, Sara L.; Eisenbeis, Scott; Guerra, Norma E.; Krolczyk, Stan; Miller, Nicole; Morales, Ana; Ramesan, Prameela; Sarafrazi, Soodabeh; Truty, Rebecca; Dahir, Kathryn Journal: Journal of bone and mineral research Issue: Volume 37:Number 2(2022) Page Start: 202 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Novel PHEX gene locus‐specific database: Comprehensive characterization of vast number of variants associated with X‐linked hypophosphatemia (XLH). Issue 2 (5th December 2021) Authors: Sarafrazi, Soodabeh; Daugherty, Sean C.; Miller, Nicole; Boada, Patrick; Carpenter, Thomas O.; Chunn, Lauren; Dill, Kariena; Econs, Michael J.; Eisenbeis, Scott; Imel, Erik A.; Johnson, Britt; Kiel, Mark J.; Krolczyk, Stan; Ramesan, Prameela; Truty, Rebecca; Sabbagh, Yves Journal: Human mutation Issue: Volume 43:Issue 2(2022) Page Start: 143 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Operation-related Musculoskeletal Injuries among United States Surgeons: A Gender-stratified National Survey. Issue 2 (18th February 2022) Authors: Tran, Maria; Kortz, Michael W.; Johnson, Britt; Janis, Jeffrey E. Journal: Plastic and reconstructive surgery Issue: Volume 10:Issue 2(2022) Page Start: e4142 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Operation-related Musculoskeletal Injuries among United States Surgeons: A Gender-stratified National Survey. Issue 2 (February 2022) Authors: Tran, Maria; Kortz, Michael W.; Johnson, Britt; Janis, Jeffrey E. Journal: Plastic and reconstructive surgery Issue: Volume 10:Issue 2(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with childhood epilepsy. Issue 3 (1st July 2019) Authors: Truty, Rebecca; Patil, Nila; Sankar, Raman; Sullivan, Joseph; Millichap, John; Carvill, Gemma; Entezam, Ali; Esplin, Edward D.; Fuller, Amy; Hogue, Michelle; Johnson, Britt; Khouzam, Amirah; Kobayashi, Yuya; Lewis, Rachel; Nykamp, Keith; Riethmaier, Darlene; Westbrook, Jody; Zeman, Michelle; Nuss... Journal: Epilepsia open Issue: Volume 4:Issue 3(2019) Page Start: 397 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Scalable detection of technically challenging variants through modified next‐generation sequencing. Issue 12 (17th October 2022) Authors: Rojahn, Susan; Hambuch, Tina; Adrian, Jessika; Gafni, Erik; Gileta, Alex; Hatchell, Hannah; Johnson, Britt; Kallman, Ben; Karfilis, Kate; Kautzer, Curtis; Kennemer, Michael; Kirk, Lloyd; Kvitek, Daniel; Lettes, Jessica; Macrae, Fenner; Mendez, Fernando; Paul, Joshua; Pellegrino, Maurizio; Preciad... Journal: Molecular genetics & genomic medicine Issue: Volume 10:Issue 12(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Severe SOPH syndrome due to a novel NBAS mutation in a 27‐year‐old woman—Review of this pleiotropic, autosomal recessive disorder: Mystery solved after two decades. Issue 7 (16th April 2020) Authors: Lacassie, Yves; Johnson, Britt; Lay‐Son, Guillermo; Quintana, Rita; King, Andrew; Cortes, Fanny; Alvarez, Cecilia; Gomez, Ricardo; Vargas, Alfonso; Chalew, Stuart; King, Alejandra; Guardia, Sylvia; Sorensen, Ricardo U.; Aradhya, Swaroop Journal: American journal of medical genetics Issue: Volume 182:Issue 7(2020) Page Start: 1767 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗