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



Siddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, David H Ledbetter, Christa L Martin, Wendy K Chung, Helen V Firth, Thomas Frazier, Robin L Hansen, Lisa Prock, Han Brunner, Ny Hoang, Stephen W Scherer, Mustafa Sahin, David T Miller. Genet Med 2019
Times Cited: 86




List of shared articles



Times cited

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

Genetic and metabolic investigations for individuals with neurodevelopmental disorders: A survey of Canadian geneticists' practices.
Melissa T Carter, Mireille Cloutier, Anne Tsampalieros, Richard Webster. Am J Med Genet A 2021
0

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



Need for psychiatric phenotyping in patients with rare genetic disorders.
Franziska Degenhardt, Gertraud Gradl-Dietsch, Johannes Hebebrand. Eur Child Adolesc Psychiatry 2021
0

Diagnostic yield of additional exome sequencing after the detection of long continuous stretches of homozygosity (LCSH) in SNP arrays.
Yanjie Fan, Lili Wang, Yu Sun, Ting Xu, Zhuwen Gong, Qianfeng Zhao, Wenjuan Qiu, Lili Liang, Bing Xiao, Huiwen Zhang,[...]. J Hum Genet 2021
0

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


Genetic diagnoses in pediatric patients with epilepsy and comorbid intellectual disability.
Mei Yang, Bocheng Xu, Jiamin Wang, Zhu Zhang, Hanbing Xie, He Wang, Ting Hu, Shanling Liu. Epilepsy Res 2021
0

Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders.
Bekim Sadikovic, Michael A Levy, Jennifer Kerkhof, Erfan Aref-Eshghi, Laila Schenkel, Alan Stuart, Haley McConkey, Peter Henneman, Andrea Venema, Charles E Schwartz,[...]. Genet Med 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

Towards a Change in the Diagnostic Algorithm of Autism Spectrum Disorders: Evidence Supporting Whole Exome Sequencing as a First-Tier Test.
Ana Arteche-López, Maria José Gómez Rodríguez, Maria Teresa Sánchez Calvin, Juan Francisco Quesada-Espinosa, Jose Miguel Lezana Rosales, Carmen Palma Milla, Irene Gómez-Manjón, Irene Hidalgo Mayoral, Rubén Pérez de la Fuente, Arancha Díaz de Bustamante,[...]. Genes (Basel) 2021
0

A Simple Practical Guide to Genomic Diagnostics in a Pediatric Setting.
Alan Taylor, Zeinab Alloub, Ahmad Abou Tayoun. Genes (Basel) 2021
0