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Author/Creator Chisholm, Caitlin

1. Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing data. Issue 3 (29th November 2022)

Authors:
Hartley, Taila; Soubry, Élisabeth; Acker, Meryl; Osmond, Matthew; Couse, Madeline; Gillespie, Meredith K.; Ito, Yoko; Marshall, Aren E.; Lemire, Gabrielle; Huang, Lijia; Chisholm, Caitlin; Eaton, Alison J.; Price, E. Magda; Dowling, James J.; Ramani, Arun K.; Mendoza‐Londono, Roberto; Costain, Gr...
Journal:
Clinical genetics
Issue:
Volume 103:Issue 3(2023)
Page Start:
288
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Homozygous WNT9B variants in two families with bilateral renal agenesis/hypoplasia/dysplasia. Issue 10 (19th June 2021)

Authors:
Lemire, Gabrielle; Zheng, Bixia; Ediae, Grace U.; Zou, Ruobing; Bhola, Priya T.; Chisholm, Caitlin; de Nanassy, Joseph; Lo, Bryan; Wang, Chunyan; Shril, Shirlee; El Desoky, Sherif; Shalaby, Mohammed; Kari, Jameela A.; Wang, Xueqi; Kernohan, Kristin D.; Boycott, Kym M.; Hildebrandt, Friedhelm; Saw...
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 10(2021)
Page Start:
3005
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Leveraging the power of new molecular technologies in the clinical setting requires unprecedented awareness of limitations and drawbacks: experience of one diagnostic laboratory. Issue 6 (21st September 2018)

Authors:
Nfonsam, Landry; Ordorica, Shelley; Ghani, Mahdi; Potter, Ryan; Schaffer, Audrey; Daoud, Hussein; Vasli, Nasim; Chisholm, Caitlin; Sinclair-Bourque, Elizabeth; McGowan-Jordan, Jean; Smith, Amanda C; Jarinova, Olga; Bronicki, Lucas
Journal:
Journal of medical genetics
Issue:
Volume 56:Issue 6(2019)
Page Start:
408
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. The implementation of an enhanced clinical model to improve the diagnostic yield of exome sequencing for patients with a rare genetic disease: A Canadian experience. Issue 2 (4th November 2022)

Authors:
Ediae, Grace Uwaila; Lemire, Gabrielle; Chisholm, Caitlin; Hartley, Taila; Eaton, Alison; Osmond, Matthew; Rojas, Samantha K.; Huang, Lijia; Gillespie, Meredith; Sawyer, Sarah L.; Boycott, Kym M.
Journal:
American journal of medical genetics
Issue:
Volume 191:Issue 2(2023)
Page Start:
338
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗