1. Characterization of a novel transgenic mouse line expressing Cre recombinase under the control of the Cdx2 neural specific enhancer. Issue 11 (30th August 2013) Authors: Coutaud, Baptiste; Pilon, Nicolas Journal: Genesis Issue: Volume 51:Issue 11(2013:Nov.) Page Start: 777 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. CHARGE syndrome‐associated proteins FAM172A and CHD7 influence male sex determination and differentiation through transcriptional and alternative splicing mechanisms. Issue 3 (7th February 2022) Authors: Bélanger, Catherine; Cardinal, Tatiana; Leduc, Elizabeth; Viger, Robert S.; Pilon, Nicolas Journal: FASEB journal Issue: Volume 36:Issue 3(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Chromatin remodeller CHD7 is required for GABAergic neuron development by promoting PAQR3 expression. (26th April 2021) Authors: Jamadagni, Priyanka; Breuer, Maximilian; Schmeisser, Kathrin; Cardinal, Tatiana; Kassa, Betelhem; Parker, J Alex; Pilon, Nicolas; Samarut, Eric; Patten, Shunmoogum A Journal: EMBO reports Issue: Volume 22:Number 6(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Dhh‐expressing Schwann cell precursors contribute to skin and cochlear melanocytes, but not to vestibular melanocytes. (3rd November 2020) Authors: Bonnamour, Grégoire; Soret, Rodolphe; Pilon, Nicolas Journal: Pigment cell & melanoma research Issue: Volume 34:Number 3(2021) Page Start: 648 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. HLX is a candidate gene for a pattern of anomalies associated with congenital diaphragmatic hernia, short bowel, and asplenia. Issue 11 (12th September 2017) Authors: Farrell, Sandra A.; Sodhi, Sandi; Marshall, Christian R.; Guerin, Andrea; Slavotinek, Anne; Paton, Tara; Chong, Karen; Sirkin, Wilma L.; Scherer, Stephen W.; Bérubé‐Simard, Félix‐Antoine; Pilon, Nicolas Journal: American journal of medical genetics Issue: Volume 173:Issue 11(2017) Page Start: 3070 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. HLX is a candidate gene for a pattern of anomalies associated with congenital diaphragmatic hernia, short bowel, and asplenia. Issue 11 (12th September 2017) Authors: Farrell, Sandra A.; Sodhi, Sandi; Marshall, Christian R.; Guerin, Andrea; Slavotinek, Anne; Paton, Tara; Chong, Karen; Sirkin, Wilma L.; Scherer, Stephen W.; Bérubé‐Simard, Félix‐Antoine; Pilon, Nicolas Journal: American journal of medical genetics Issue: Volume 173:Issue 11(2017) Page Start: 3070 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Molecular dissection of CHARGE syndrome highlights the vulnerability of neural crest cells to problems with alternative splicing and other transcription-related processes. Issue 1 (1st January 2019) Authors: Bérubé-Simard, Félix-Antoine; Pilon, Nicolas Journal: Transcription Issue: Volume 10:Issue 1(2019) Page Start: 21 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. NR2F1 regulates a Schwann cell precursor‐vs‐melanocyte cell fate switch in a mouse model of Waardenburg syndrome type IV. (16th July 2022) Authors: Bonnamour, Grégoire; Charrier, Baptiste; Sallis, Sephora; Leduc, Elizabeth; Pilon, Nicolas Journal: Pigment cell & melanoma research Issue: Volume 35:Number 5(2022) Page Start: 506 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Pigmentation-based insertional mutagenesis is a simple and potent screening approach for identifying neurocristopathy-associated genes in mice. Issue 1 (1st January 2016) Authors: Pilon, Nicolas Journal: Rare diseases Issue: Volume 4:Issue 1(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Toward a better understanding of enteric gliogenesis. Issue 1 (1st January 2017) Authors: Charrier, Baptiste; Pilon, Nicolas Journal: Neurogenesis Issue: Volume 4:Issue 1(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗