1. A deleterious mutation in the PEX2 gene causes Zellweger syndrome in individuals of Ashkenazi Jewish descent. (3rd May 2013) Authors: Fedick, A.; Jalas, C.; Treff, N.R. Journal: Clinical genetics Issue: Volume 85:Number 4(2014:Apr.) Page Start: 343 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A founder mutation in the TCIRG1 gene causes osteopetrosis in the Ashkenazi Jewish population. (31st July 2014) Authors: Anderson, S.L.; Jalas, C.; Fedick, A.; Reid, K.F.; Carpenter, T.O.; Chirnomas, D.; Treff, N.R.; Ekstein, J.; Rubin, B.Y. Journal: Clinical genetics Issue: Volume 88:Number 1(2015:Jul.) Page Start: 74 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Carrier frequency of two BBS2 mutations in the Ashkenazi population. (28th July 2013) Authors: Fedick, A.; Jalas, C.; Abeliovich, D.; Krakinovsky, Y.; Ekstein, J.; Ekstein, A.; Treff, N.R. Journal: Clinical genetics Issue: Volume 85:Number 6(2014:Jun.) Page Start: 578 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Carrier screening of RTEL1 mutations in the Ashkenazi Jewish population. (5th September 2014) Authors: Fedick, A.M.; Shi, L.; Jalas, C.; Treff, N.R.; Ekstein, J.; Kornreich, R.; Edelmann, L.; Mehta, L.; Savage, S.A. Journal: Clinical genetics Issue: Volume 88:Number 2(2015:Aug.) Page Start: 177 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Carrier screening of RTEL1 mutations in the Ashkenazi Jewish population. (5th September 2014) Authors: Fedick, A.M.; Shi, L.; Jalas, C.; Treff, N.R.; Ekstein, J.; Kornreich, R.; Edelmann, L.; Mehta, L.; Savage, S.A. Journal: Clinical genetics Issue: Volume 88:Number 2(2015:Aug.) Page Start: 177 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Characterizing the microbiome at embryo transfer: next generation sequencing of the 16S ribosomal gene. (October 2016) Authors: Franasiak, J.M.; Tao, X.; Zhan, Y.; Chu, T.C.; Treff, N.R.; Scott, R.T. Journal: Reproductive biomedicine online Issue: Volume 33(2016)Supplement 1 Page Start: e3 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Uterine natural killer cell immunoglobulin receptor (KIR) genotypes and trophoblastic human leukocyte antigen C (HLA-C) ligands influence risk of pregnancy loss: data from euploid transfers. (October 2016) Authors: Morin, S.J.; Franasiak, J.M.; Juneau, C.R.; Han, M.; Treff, N.R.; Scott, R.T. Journal: Reproductive biomedicine online Issue: Volume 33(2016)Supplement 1 Page Start: e1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗