A citation-based method for searching scientific literature

David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein, W Andrew Faucett, Lars Feuk, Jan M Friedman, Ada Hamosh, Laird Jackson, Erin B Kaminsky, Klaas Kok, Ian D Krantz, Robert M Kuhn, Charles Lee, James M Ostell, Carla Rosenberg, Stephen W Scherer, Nancy B Spinner, Dimitri J Stavropoulos, James H Tepperberg, Erik C Thorland, Joris R Vermeesch, Darrel J Waggoner, Michael S Watson, Christa Lese Martin, David H Ledbetter. Am J Hum Genet 2010
Times Cited: 1457



Michelle M Clark, Zornitza Stark, Lauge Farnaes, Tiong Y Tan, Susan M White, David Dimmock, Stephen F Kingsmore. NPJ Genom Med 2018
Times Cited: 137




List of shared articles



Times cited

Diagnostic yield and treatment impact of whole-genome sequencing in paediatric neurological disorders.
Hsiu-Fen Lee, Ching-Shiang Chi, Chi-Ren Tsai. Dev Med Child Neurol 2021
0

Outcomes of prior authorization requests for genetic testing in outpatient pediatric genetics clinics.
Hadley Stevens Smith, Rachel Franciskovich, Andrea M Lewis, Amanda Gerard, Rebecca O Littlejohn, Kimberly Nugent, Janah Rodriguez, Haley Streff. Genet Med 2021
0

Genetic Disease and Therapy.
Theodore L Roth, Alexander Marson. Annu Rev Pathol 2021
0

Diagnostic and clinical utility of next-generation sequencing in children born with multiple congenital anomalies in the China neonatal genomes project.
Huijun Wang, Feifan Xiao, Xinran Dong, Yulan Lu, Guoqiang Cheng, Laishuan Wang, Wei Lu, Lin Yang, Liping Chen, Wenqing Kang,[...]. Hum Mutat 2021
0

Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia.
Bahareh A Mojarad, Yue Yin, Roozbeh Manshaei, Ian Backstrom, Gregory Costain, Tracy Heung, Daniele Merico, Christian R Marshall, Anne S Bassett, Ryan K C Yuen. Transl Psychiatry 2021
0

Genetic Testing in Neurodevelopmental Disorders.
Juliann M Savatt, Scott M Myers. Front Pediatr 2021
1

Population Genomic Screening for Genetic Etiologies of Neurodevelopmental/Psychiatric Disorders Demonstrates Personal Utility and Positive Participant Responses.
Karen E Wain, Kasia Tolwinski, Emily Palen, Alexis R Heidlebaugh, Karahlyn Holdren, Lauren Kasparson Walsh, Matthew T Oetjens, David H Ledbetter, Christa Lese Martin. J Pers Med 2021
0

Adaptation and validation of the Genetic Counseling Outcome Scale for autism spectrum disorders and related conditions.
Afiqah Yusuf, Iskra Peltekova, Tal Savion-Lemieux, Jennifer Frei, Ridha Joober, Jennifer Howe, Stephen W Scherer, Mayada Elsabbagh. J Genet Couns 2021
1

Cost-effectiveness of genome-wide sequencing for unexplained developmental disabilities and multiple congenital anomalies.
Chunmei Li, Stacey Vandersluis, Corinne Holubowich, Wendy J Ungar, Elaine S Goh, Kym M Boycott, Nancy Sikich, Irfan Dhalla, Vivian Ng. Genet Med 2021
1

PLXNA2 and LRRC40 as candidate genes in autism spectrum disorder.
Jordi Pijuan, Juan Darío Ortigoza-Escobar, Juan Ortiz, Adrián Alcalá, María José Calvo, Mariona Cubells, Cristina Hernando-Davalillo, Francesc Palau, Janet Hoenicka. Autism Res 2021
0

Comparison of the diagnostic yield of aCGH and genome-wide sequencing across different neurodevelopmental disorders.
Francisco Martinez-Granero, Fiona Blanco-Kelly, Carolina Sanchez-Jimeno, Almudena Avila-Fernandez, Ana Arteche, Ana Bustamante-Aragones, Cristina Rodilla, Elvira Rodríguez-Pinilla, Rosa Riveiro-Alvarez, Saoud Tahsin-Swafiri,[...]. NPJ Genom Med 2021
0

Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability.
Jennifer Malinowski, David T Miller, Laurie Demmer, Jennifer Gannon, Elaine Maria Pereira, Molly C Schroeder, Maren T Scheuner, Anne Chun-Hui Tsai, Scott E Hickey, Jun Shen. Genet Med 2020
11