1. 169 Exome Sequencing Implicates Endothelial Ras Signaling Network in Vein of Galen Aneurysmal Malformation. (April 2023) Authors: Mekbib, Kedous Y.; Zhao, Shujuan; Nelson-Williams, Carol; Prendergast, Andrew; Zeng, Xue; Rolle, Myron; Shohfi, John; Smith, Hannah; Ocken, Jack; Moyer, Quentin; Piwowarczyk, Paulina; Allington, Garrett; Dong, Weilai; van der Ent, Martijn A.; Chen, Di; Li, Boyang; Duran, Daniel; Mane, Shrikant M.... Journal: Neurosurgery Issue: Volume 69(2023)Supplement 1 Page Start: 22 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A phase 2 evaluation of pembrolizumab for recurrent Lynch‐like versus sporadic endometrial cancers with microsatellite instability. Issue 6 (7th December 2021) Authors: Bellone, Stefania; Roque, Dana M.; Siegel, Eric R.; Buza, Natalia; Hui, Pei; Bonazzoli, Elena; Guglielmi, Adele; Zammataro, Luca; Nagarkatti, Nupur; Zaidi, Samir; Lee, Jungsoo; Silasi, Dan‐Arin; Huang, Gloria S.; Andikyan, Vaagn; Damast, Shari; Clark, Mitchell; Azodi, Masoud; Schwartz, Peter E.; ... Journal: Cancer Issue: Volume 128:Issue 6(2022) Page Start: 1206 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clonal evolution analysis of paired anaplastic and well‐differentiated thyroid carcinomas reveals shared common ancestor. Issue 12 (24th September 2018) Authors: Dong, Weilai; Nicolson, Norman G.; Choi, Jungmin; Barbieri, Andrea L.; Kunstman, John W.; Abou Azar, Sara; Knight, James; Bilguvar, Kaya; Mane, Shrikant M.; Lifton, Richard P.; Korah, Reju; Carling, Tobias Journal: Genes, chromosomes & cancer Issue: Volume 57:Issue 12(2018) Page Start: 645 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Exome Sequencing Implicates SWI/SNF Chromatin Remodeling Genes in Human Congenital Hydrocephalus. (1st September 2019) Authors: Allocco, August A; Jin, Sheng Chih; Dong, Weilai; Zeng, Xue; Conine, Sierra B; Furey, Charuta Gavankar; Date, Priya Prakash; Gaillard, Jonathan; Nelson-Williams, Carol; Dunbar, Ashley; DeSpenza, Tyrone; Deniz, Engin; Khokha, Mustafa Kezar; Lifton, Richard P; Kahle, Kristopher T Journal: Neurosurgery Issue: Volume 66(2010)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Exome Sequencing Implicates SWI/SNF Chromatin Remodeling Genes in Human Congenital Hydrocephalus. (September 2019) Authors: Allocco, August A; Jin, Sheng Chih; Dong, Weilai; Zeng, Xue; Conine, Sierra B; Furey, Charuta Gavankar; Date, Priya Prakash; Gaillard, Jonathan; Nelson‐Williams, Carol; Dunbar, Ashley; DeSpenza, Tyrone; Deniz, Engin; Khokha, Mustafa Kezar; Lifton, Richard P; Kahle, Kristopher T Journal: Neurosurgery Issue: Volume 66(2019)Supplement Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. GemC1 is a critical switch for neural stem cell generation in the postnatal brain. Issue 12 (22nd July 2019) Authors: Lalioti, Maria‐Eleni; Kaplani, Konstantina; Lokka, Georgia; Georgomanolis, Theodore; Kyrousi, Christina; Dong, Weilai; Dunbar, Ashley; Parlapani, Evangelia; Damianidou, Eleni; Spassky, Nathalie; Kahle, Kristopher T.; Papantonis, Argyris; Lygerou, Zoi; Taraviras, Stavros Journal: Glia Issue: Volume 67:Issue 12(2019) Page Start: 2360 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Identification of a dominant MYH11 causal variant in chronic intestinal pseudo‐obstruction: Results of whole‐exome sequencing. Issue 5 (13th August 2019) Authors: Dong, Weilai; Baldwin, Clinton; Choi, Jungmin; Milunsky, Jeff M.; Zhang, Junhui; Bilguvar, Kaya; Lifton, Richard P.; Milunsky, Aubrey Journal: Clinical genetics Issue: Volume 96:Issue 5(2019) Page Start: 473 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Integrative Genomics Implicates Genetic Disruption of Prenatal Neurogenesis in Congenital Hydrocephalus. (16th November 2020) Authors: Panchagnula, Shreyas; Jin, Sheng C; Dong, Weilai; Kundishora, Adam; Moreno-De-Luca, Andres; Furey, Charuta G; Allocco, August A; Walker, Rebecca; Nelson-Williams, Carol; Smith, Hannah; Dunbar, Ashley; Conine, Sierra B; Lu, Qiongshi; Zen, Xue; Sierant, Michael; Knight, James; Sullivan, William; Ph... Journal: Neurosurgery Issue: Volume 67(2010)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Mutation spectrum of congenital heart disease in a consanguineous Turkish population. Issue 6 (28th April 2022) Authors: Dong, Weilai; Kaymakcalan, Hande; Jin, Sheng Chih; Diab, Nicholas S.; Tanıdır, Cansaran; Yalcin, Ali Seyfi Yalim; Ercan‐Sencicek, A. Gulhan; Mane, Shrikant; Gunel, Murat; Lifton, Richard P.; Bilguvar, Kaya; Brueckner, Martina Journal: Molecular genetics & genomic medicine Issue: Volume 10:Issue 6(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Nonexercise machine learning models for maximal oxygen uptake prediction in national population surveys. (11th March 2023) Authors: Liu, Yuntian; Herrin, Jeph; Huang, Chenxi; Khera, Rohan; Dhingra, Lovedeep Singh; Dong, Weilai; Mortazavi, Bobak J; Krumholz, Harlan M; Lu, Yuan Journal: Journal of the American Medical Informatics Association Issue: Volume 30:Number 5(2023) Page Start: 943 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗