Works by Dong, Weilai

Results: 25

DIAPH1 Variants in Non–East Asian Patients With Sporadic Moyamoya Disease.

Published in:

JAMA Neurology, 2021, v. 78, n. 8, p. 993, doi. 10.1001/jamaneurol.2021.1681

By:

Kundishora, Adam J.;
Peters, Samuel T.;
Pinard, Amélie;
Duran, Daniel;
Panchagnula, Shreyas;
Barak, Tanyeri;
Miyagishima, Danielle F.;
Dong, Weilai;
Smith, Hannah;
Ocken, Jack;
Dunbar, Ashley;
Nelson-Williams, Carol;
Haider, Shozeb;
Walker, Rebecca L.;
Li, Boyang;
Zhao, Hongyu;
Thumkeo, Dean;
Marlier, Arnaud;
Duy, Phan Q.;
Diab, Nicholas S.

Publication type:

Article

Simulation study on catalytic oxidation of low concentration mine gas in an oxidation device.

Published in:

Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-024-80225-4

By:

Liu, Yuhang;
Li, Xijian;
Xiao, Qi;
Jiang, Xingfa;
Dong, Weilai;
Chen, Xianyong;
Feng, Yuyan

Publication type:

Article

A Novel Missense Mutation in ERCC8 Co-Segregates with Cerebellar Ataxia in a Consanguineous Pakistani Family.

Published in:

Cells (2073-4409), 2022, v. 11, n. 19, p. 3090, doi. 10.3390/cells11193090

By:

Gauhar, Zeeshan;
Tejwani, Leon;
Abdullah, Uzma;
Saeed, Sadia;
Shafique, Shagufta;
Badshah, Mazhar;
Choi, Jungmin;
Dong, Weilai;
Nelson-Williams, Carol;
Lifton, Richard P.;
Lim, Janghoo;
Raja, Ghazala K.

Publication type:

Article

Identification of a dominant MYH11 causal variant in chronic intestinal pseudo‐obstruction: Results of whole‐exome sequencing.

Published in:

Clinical Genetics, 2019, v. 96, n. 5, p. 473, doi. 10.1111/cge.13617

By:

Dong, Weilai;
Baldwin, Clinton;
Choi, Jungmin;
Milunsky, Jeff M.;
Zhang, Junhui;
Bilguvar, Kaya;
Lifton, Richard P.;
Milunsky, Aubrey

Publication type:

Article

The Cost of Medications at a Student-Run Free Clinic in New Haven, Connecticut, 2021-2023.

Published in:

Preventing Chronic Disease, 2024, v. 21, p. 1, doi. 10.5888/pcd21.230277

By:

See, Claudia;
Hegde, Krupa;
Reid, Lucy;
Shi, Ryan;
Luthra, Ragini;
Weilai Dong;
Lee, Viola;
Kang-Giaimo, Angela

Publication type:

Article

Molecular Genetics and Complex Inheritance of Congenital Heart Disease.

Published in:

Genes, 2021, v. 12, n. 7, p. 1020, doi. 10.3390/genes12071020

By:

Diab, Nicholas S.;
Barish, Syndi;
Dong, Weilai;
Zhao, Shujuan;
Allington, Garrett;
Yu, Xiaobing;
Kahle, Kristopher T.;
Brueckner, Martina;
Jin, Sheng Chih

Publication type:

Article

Statistical methods for assessing the effects of de novo variants on birth defects.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00590-z

By:

Xie, Yuhan;
Wu, Ruoxuan;
Li, Hongyu;
Dong, Weilai;
Zhou, Geyu;
Zhao, Hongyu

Publication type:

Article

GemC1 is a critical switch for neural stem cell generation in the postnatal brain.

Published in:

Glia (0894-1491), 2019, v. 67, n. 12, p. 2360, doi. 10.1002/glia.23690

By:

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

Publication type:

Article

Nonexercise machine learning models for maximal oxygen uptake prediction in national population surveys.

Published in:

Journal of the American Medical Informatics Association, 2023, v. 30, n. 5, p. 943, doi. 10.1093/jamia/ocad035

By:

Liu, Yuntian;
Herrin, Jeph;
Huang, Chenxi;
Khera, Rohan;
Dhingra, Lovedeep Singh;
Dong, Weilai;
Mortazavi, Bobak J;
Krumholz, Harlan M;
Lu, Yuan

Publication type:

Article

Network assisted analysis of De novo variants using protein-protein interaction information identified 46 candidate genes for congenital heart disease.

Published in:

PLoS Genetics, 2022, v. 18, n. 6, p. 1, doi. 10.1371/journal.pgen.1010252

By:

Xie, Yuhan;
Jiang, Wei;
Dong, Weilai;
Li, Hongyu;
Jin, Sheng Chih;
Brueckner, Martina;
Zhao, Hongyu

Publication type:

Article

M-DATA: A statistical approach to jointly analyzing de novo mutations for multiple traits.

Published in:

PLoS Genetics, 2021, v. 17, n. 11, p. 1, doi. 10.1371/journal.pgen.1009849

By:

Xie, Yuhan;
Li, Mo;
Dong, Weilai;
Jiang, Wei;
Zhao, Hongyu

Publication type:

Article

TRIM71 mutations cause a neurodevelopmental syndrome featuring ventriculomegaly and hydrocephalus.

Published in:

Brain: A Journal of Neurology, 2024, v. 147, n. 12, p. 4292, doi. 10.1093/brain/awae175

By:

Duy, Phan Q;
Jux, Bettina;
Zhao, Shujuan;
Mekbib, Kedous Y;
Dennis, Evan;
Dong, Weilai;
Nelson-Williams, Carol;
Mehta, Neel H;
Shohfi, John P;
Juusola, Jane;
Allington, Garrett;
Smith, Hannah;
Marlin, Sandrine;
Belhous, Kahina;
Monteleone, Berrin;
Schaefer, G Bradley;
Pisarska, Margareta D;
Vásquez, Jaime;
Estrada-Veras, Juvianee I;
Keren, Boris

Publication type:

Article

Correction to: A contiguous microdeletion syndrome at Xp22.13 with non-obstructive azoospermia and congenital cataracts.

Published in:

2021

By:

Milunsky, Aubrey;
Milunsky, Jeff M.;
Dong, Weilai;
Hovhannisyan, Hayk;
Oates, Robert D.

Publication type:

Correction Notice

A contiguous microdeletion syndrome at Xp23.13 with non-obstructive azoospermia and congenital cataracts.

Published in:

Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 2, p. 471, doi. 10.1007/s10815-019-01685-6

By:

Milunsky, Aubrey;
Milunsky, Jeff M.;
Dong, Weilai;
Hovhannisyan, Hayk;
Oates, Robert D.

Publication type:

Article

Clonal evolution analysis of paired anaplastic and well‐differentiated thyroid carcinomas reveals shared common ancestor.

Published in:

Genes, Chromosomes & Cancer, 2018, v. 57, n. 12, p. 645, doi. 10.1002/gcc.22678

By:

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

Publication type:

Article

Integrative modeling of transmitted and de novo variants identifies novel risk genes for congenital heart disease.

Published in:

Quantitative Biology, 2021, v. 9, n. 2, p. 216, doi. 10.15302/J-QB-021-0248

By:

Mo Li;
Xue Zeng;
Jin, Chentian;
Sheng Chih Jin;
Weilai Dong;
Brueckner, Martina;
Lifton, Richard;
Qiongshi Lu;
Hongyu Zhao

Publication type:

Article

Clinical Biochemistry of Serum Troponin.

Published in:

Diagnostics (2075-4418), 2024, v. 14, n. 4, p. 378, doi. 10.3390/diagnostics14040378

By:

Gokhan, Ilhan;
Dong, Weilai;
Grubman, Daniel;
Mezue, Kenechukwu;
Yang, David;
Wang, Yanting;
Gandhi, Parul U.;
Kwan, Jennifer M.;
Hu, Jiun-Ruey

Publication type:

Article

Clinical, demographic and genetic features of patients with congenital heart disease : A single center experience.

Published in:

Marmara Medical Journal, 2022, v. 35, n. 2, p. 159, doi. 10.5472/marumj.1120570

By:

KAYMAKCALAN, Hande;
YALCINKAYA, Leyla;
NIKEREL, Emrah;
YALCIN, Yalim;
Weilai DONG;
ERCAN SENCICEK, Adife Gulhan

Publication type:

Article

Recessive Inheritance of Congenital Hydrocephalus With Other Structural Brain Abnormalities Caused by Compound Heterozygous Mutations in ATP1A3.

Published in:

Frontiers in Cellular Neuroscience, 2019, p. 1, doi. 10.3389/fncel.2019.00425

By:

Allocco, August A.;
Jin, Sheng Chih;
Duy, Phan Q.;
Furey, Charuta G.;
Zeng, Xue;
Dong, Weilai;
Nelson-Williams, Carol;
Karimy, Jason K.;
DeSpenza, Tyrone;
Hao, Le T.;
Reeves, Benjamin;
Haider, Shozeb;
Gunel, Murat;
Lifton, Richard P.;
Kahle, Kristopher T.

Publication type:

Article

Comprehensive Genetic Analysis of Follicular Thyroid Carcinoma Predicts Prognosis Independent of Histology.

Published in:

2018

By:

Nicolson, Norman G;
Murtha, Timothy D;
Dong, Weilai;
Paulsson, Johan O;
Choi, Jungmin;
Barbieri, Andrea L;
Brown, Taylor C;
Kunstman, John W;
Larsson, Catharina;
Prasad, Manju L;
Korah, Reju;
Lifton, Richard P;
Juhlin, C Christofer;
Carling, Tobias

Publication type:

journal article

A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome.

Published in:

2022

By:

Kaymakçalan, Hande;
Ercan-Şençiçek, A. Gülhan;
Cebeci, Ayşe Nurcan;
Dong, Weilai;
Yalçın, Ali Seyfi Yalım

Publication type:

Case Study

Mutation spectrum of congenital heart disease in a consanguineous Turkish population.

Published in:

Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 6, p. 1, doi. 10.1002/mgg3.1944

By:

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

Publication type:

Article

SLC12A ion transporter mutations in sporadic and familial human congenital hydrocephalus.

Published in:

Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 9, p. N.PAG, doi. 10.1002/mgg3.892

By:

Jin, Sheng Chih;
Furey, Charuta G.;
Zeng, Xue;
Allocco, August;
Nelson‐Williams, Carol;
Dong, Weilai;
Karimy, Jason K.;
Wang, Kevin;
Ma, Shaojie;
Delpire, Eric;
Kahle, Kristopher T.

Publication type:

Article

Exome Sequencing as a Potential Diagnostic Adjunct in Sporadic Congenital Hydrocephalus.

Published in:

JAMA Pediatrics, 2021, v. 175, n. 3, p. 310, doi. 10.1001/jamapediatrics.2020.4878

By:

Sullivan, William;
Reeves, Benjamin C.;
Duy, Phan Q.;
Nelson-Williams, Carol;
Dong, Weilai;
Jin, Sheng Chih;
Kahle, Kristopher T.

Publication type:

Article

Dual inhibiting OCT4 and AKT potently suppresses the propagation of human cancer cells.

Published in:

Scientific Reports, 2017, p. 46246, doi. 10.1038/srep46246

By:

Li, Wenxin;
Zhou, Yanwen;
Zhang, Xiaoqian;
Yang, Ying;
Dan, Songsong;
Su, Tong;
She, Shiqi;
Dong, Weilai;
Zhao, Qingwei;
Jia, Jia;
Yao, Hangping;
Zheng, Min;
Kang, Bo;
Wang, Ying-Jie

Publication type:

Article