1. A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals. Issue 6 (6th June 2019) Authors: Carlson, Jenna C.; Anand, Deepti; Butali, Azeez; Buxo, Carmen J.; Christensen, Kaare; Deleyiannis, Frederic; Hecht, Jacqueline T.; Moreno, Lina M.; Orioli, Ieda M.; Padilla, Carmencita; Shaffer, John R.; Vieira, Alexandre R.; Wehby, George L.; Weinberg, Seth M.; Murray, Jeffrey C.; Beaty, Terri H... Journal: Genetic epidemiology Issue: Volume 43:Issue 6(2019) Page Start: 704 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Cover Image, Volume 39, Issue 4. Issue 4 (6th March 2018) Authors: Anand, Deepti; Agrawal, Smriti A.; Slavotinek, Anne; Lachke, Salil A. Journal: Human mutation Issue: Volume 39:Issue 4(2018) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Exome sequencing provides additional evidence for the involvement of ARHGAP29 in Mendelian orofacial clefting and extends the phenotypic spectrum to isolated cleft palate. Issue 1 (20th January 2017) Authors: Liu, Huan; Busch, Tamara; Eliason, Steven; Anand, Deepti; Bullard, Steven; Gowans, Lord J.J; Nidey, Nichole; Petrin, Aline; Augustine‐Akpan, Eno‐Abasi; Saadi, Irfan; Dunnwald, Martine; Lachke, Salil A.; Zhu, Ying; Adeyemo, Adebowale; Amendt, Brad; Roscioli, Tony; Cornell, Robert; Murray, Jeffrey;... Journal: Birth defects research Issue: Volume 109:Issue 1(2017) Page Start: 27 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Front Cover, Volume 40, Issue 10. Issue 10 (27th September 2019) Authors: Cox, Timothy C.; Lidral, Andrew C.; McCoy, Jason C.; Liu, Huan; Cox, Liza L.; Zhu, Ying; Anderson, Ryan D.; Moreno Uribe, Lina M.; Anand, Deepti; Deng, Mei; Richter, Chika T.; Nidey, Nichole L.; Standley, Jennifer M.; Blue, Elizabeth E.; Chong, Jessica X.; Smith, Joshua D.; Kirk, Edwin P.; Vensel... Journal: Human mutation Issue: Volume 40:Issue 10(2019) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Identification of OAF and PVRL1 as candidate genes for an ocular anomaly characterized by Peters anomaly type 2 and ectopia lentis. (March 2018) Authors: David, Dezső; Anand, Deepti; Araújo, Carlos; Gloss, Brian; Fino, Joana; Dinger, Marcel; Lindahl, Päivi; Pöyhönen, Minna; Hannele, Laivuori; Lavinha, João Journal: Experimental eye research Issue: Volume 168(2018) Page Start: 161 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. ISyTE 2.0: a database for expression-based gene discovery in the eye. Issue Volume 46:Issue D1(2018) (19th September 2017) Authors: Kakrana, Atul; Yang, Andrian; Anand, Deepti; Djordjevic, Djordje; Ramachandruni, Deepti; Singh, Abhyudai; Huang, Hongzhan; Ho, Joshua W K; Lachke, Salil A Journal: Nucleic acids research Issue: Volume 46:Issue D1(2018) Page Start: D875 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Molecular characterization of mouse lens epithelial cell lines and their suitability to study RNA granules and cataract associated genes. (February 2015) Authors: Terrell, Anne M.; Anand, Deepti; Smith, Sylvie F.; Dang, Christine A.; Waters, Stephanie M.; Pathania, Mallika; Beebe, David C.; Lachke, Salil A. Journal: Experimental eye research Issue: Volume 131(2015:Feb.) Page Start: 42 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Molecular characterization of the human lens epithelium-derived cell line SRA01/04. (November 2019) Authors: Weatherbee, Bailey A.T.; Barton, Joshua R.; Siddam, Archana D.; Anand, Deepti; Lachke, Salil A. Journal: Experimental eye research Issue: Volume 188(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Mutation update of transcription factor genes FOXE3, HSF4, MAF, and PITX3 causing cataracts and other developmental ocular defects. Issue 4 (16th January 2018) Authors: Anand, Deepti; Agrawal, Smriti A.; Slavotinek, Anne; Lachke, Salil A. Journal: Human mutation Issue: Volume 39:Issue 4(2018) Page Start: 471 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans. Issue 10 (18th June 2019) Authors: Cox, Timothy C.; Lidral, Andrew C.; McCoy, Jason C.; Liu, Huan; Cox, Liza L.; Zhu, Ying; Anderson, Ryan D.; Moreno Uribe, Lina M.; Anand, Deepti; Deng, Mei; Richter, Chika T.; Nidey, Nichole L.; Standley, Jennifer M.; Blue, Elizabeth E.; Chong, Jessica X.; Smith, Joshua D.; Kirk, Edwin P.; Vensel... Journal: Human mutation Issue: Volume 40:Issue 10(2019) Page Start: 1813 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗