1. A 3D Fiber‐Hydrogel Based Non‐Viral Gene Delivery Platform Reveals that microRNAs Promote Axon Regeneration and Enhance Functional Recovery Following Spinal Cord Injury. Issue 15 (29th May 2021) Authors: Zhang, Na; Lin, Junquan; Lin, Vincent Po Hen; Milbreta, Ulla; Chin, Jiah Shin; Chew, Elaine Guo Yan; Lian, Michelle Mulan; Foo, Jia Nee; Zhang, Kunyu; Wu, Wutian; Chew, Sing Yian Journal: Advanced science Issue: Volume 8:Issue 15(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A recurrent missense mutation in the EDAR gene causes severe autosomal recessive hypohidrotic ectodermal dysplasia in two consanguineous Kashmiri families. (5th August 2019) Authors: Sadia, ; Foo, Jia Nee; Khor, Chiea Chuen; Jelani, Musharraf; Ali, Ghazanfar Journal: Journal of gene medicine Issue: Volume 21:Number 9(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. C9orf72 expansions are the most common cause of genetic frontotemporal dementia in a Southeast Asian cohort. Issue 4 (17th February 2023) Authors: Tan, Yi Jayne; Yong, Alisa C. W.; Foo, Jia Nee; Lian, Michelle M.; Lim, Weng Khong; Dominguez, Jacqueline; Fong, Zhi Hui; Narasimhalu, Kaavya; Chiew, Hui Jin; Ng, Kok Pin; Ting, Simon K. S.; Kandiah, Nagaendran; Ng, Adeline S. L. Journal: Annals of clinical and translational neurology Issue: Volume 10:Issue 4(2023) Page Start: 568 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. CHCHD2 and Parkinson's disease. Issue 7 (July 2015) Authors: Foo, Jia Nee; Liu, Jianjun; Tan, Eng-King Journal: Lancet neurology Issue: Volume 14:Issue 7(2015:Jul.) Page Start: 681 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Genetic risk of extranodal natural killer T-cell lymphoma: a genome-wide association study. Issue 9 (September 2016) Authors: Li, Zheng; Xia, Yi; Feng, Li-Na; Chen, Jie-Rong; Li, Hong-Min; Cui, Jing; Cai, Qing-Qing; Sim, Kar Seng; Nairismägi, Maarja-Liisa; Laurensia, Yurike; Meah, Wee Yang; Liu, Wen-Sheng; Guo, Yun-Miao; Chen, Li-Zhen; Feng, Qi-Sheng; Pang, Chi Pui; Chen, Li Jia; Chew, Soo Hong; Ebstein, Richard P; Foo,... Journal: Lancet oncology Issue: Volume 17:Issue 9(2016:Sep.) Page Start: 1240 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in BBS2 in a Kashmiri Family with Bardet-Biedl Syndrome. (23rd February 2021) Authors: Ali, Ghazanfar; Sadia, ; Foo, Jia Nee; Nasir, Abdul; Chang, Chu-Hua; Chew, Elaine GuoYan; Latif, Zahid; Azeem, Zahid; Ain-ul-Batool, Syeda; Kazmi, Syed Akif Raza; Awan, Naheed Bashir; Khan, Abdul Hameed; Rehman, Fazal-Ur-; Khalid, Madiha; Wali, Abdul; Sarwar, Samina; Akhtar, Wasim; Ahmed Abbasi, ... Other Names: Erg n Sercan Academic Editor. Journal: BioMed research international Issue: Volume 2021(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Identification of a recurrent nonsense mutation in HR gene responsible for atrichia with papular lesions in two Kashmiri families. (17th February 2020) Authors: Ali, Ghazanfar; Awan, Naheed Bashir; Sadia, ; Khawaja, Abdul Waheed; Foo, Jia Nee; Khor, Chiea Chuen; Chang, Chu‐Hua; Chew, Elaine GuoYan; Kiani, Farhat Rafique; Jelani, Musharraf Journal: Journal of gene medicine Issue: Volume 22:Number 5(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Identifying genes in Parkinson disease: state of the art. Issue 9 (21st May 2018) Authors: Chew, Elaine GY; Foo, Jia Nee; Tan, Eng‐King Journal: Medical journal of Australia Issue: Volume 208:Issue 9(2018) Page Start: 381 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Large 3‐Mb deletions at 22q11.2 locus in Parkinson's disease and schizophrenia. Issue 12 (27th October 2016) Authors: Foo, Jia Nee; Lee, Jimmy; Tan, Louis C.; Liu, Jianjun; Tan, Eng‐King Journal: Movement disorders Issue: Volume 31:Issue 12(2016) Page Start: 1924 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Large-scale genotyping identifies a new locus at 22q13.2 associated with female breast size. Issue 10 (3rd July 2013) Authors: Li, Jingmei; Foo, Jia Nee; Schoof, Nils; Varghese, Jajini S; Fernandez-Navarro, Pablo; Gierach, Gretchen L; Quek, Swee Tian; Hartman, Mikael; Nord, Silje; Kristensen, Vessela N; Pollán, Marina; Figueroa, Jonine D; Thompson, Deborah J; Li, Yi; Khor, Chiea Chuen; Humphreys, Keith; Liu, Jianjun; Cze... Journal: Journal of medical genetics Issue: Volume 50:Issue 10(2013) Page Start: 666 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗