A citation-based method for searching scientific literature

Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay, Narayanan Veeraraghavan, Alicia Hawes, Theodore Chiang, Magalie Leduc, Joke Beuten, Jing Zhang, Weimin He, Jennifer Scull, Alecia Willis, Megan Landsverk, William J Craigen, Mir Reza Bekheirnia, Asbjorg Stray-Pedersen, Pengfei Liu, Shu Wen, Wendy Alcaraz, Hong Cui, Magdalena Walkiewicz, Jeffrey Reid, Matthew Bainbridge, Ankita Patel, Eric Boerwinkle, Arthur L Beaudet, James R Lupski, Sharon E Plon, Richard A Gibbs, Christine M Eng. JAMA 2014
Times Cited: 809



Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf, Kent D McKelvey, Kelly E Ormond, C Sue Richards, Christopher N Vlangos, Michael Watson, Christa L Martin, David T Miller. Genet Med 2017
Times Cited: 831




List of shared articles



Times cited

Application of Next Generation Sequencing in Laboratory Medicine.
Yiming Zhong, Feng Xu, Jinhua Wu, Jeffrey Schubert, Marilyn M Li. Ann Lab Med 2021
8


Genetic testing in dementia - utility and clinical strategies.
Carolin A M Koriath, Joanna Kenny, Natalie S Ryan, Jonathan D Rohrer, Jonathan M Schott, Henry Houlden, Nick C Fox, Sarah J Tabrizi, Simon Mead. Nat Rev Neurol 2021
3

Improving diagnostics of rare genetic diseases with NGS approaches.
Mateja Vinkšel, Karin Writzl, Aleš Maver, Borut Peterlin. J Community Genet 2021
3

Genetic Testing in Neurodevelopmental Disorders.
Juliann M Savatt, Scott M Myers. Front Pediatr 2021
10


Randomized prospective evaluation of genome sequencing versus standard-of-care as a first molecular diagnostic test.
Deanna G Brockman, Christina A Austin-Tse, Renée C Pelletier, Caroline Harley, Candace Patterson, Holly Head, Courtney Elizabeth Leonard, Kimberly O'Brien, Lisa M Mahanta, Matthew S Lebo,[...]. Genet Med 2021
0

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG).
David T Miller, Kristy Lee, Adam S Gordon, Laura M Amendola, Kathy Adelman, Sherri J Bale, Wendy K Chung, Michael H Gollob, Steven M Harrison, Gail E Herman,[...]. Genet Med 2021
11

Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment.
Paulina Bahena, Narsis Daftarian, Reza Maroofian, Paola Linares, Daniel Villalobos, Mehraban Mirrahimi, Aboulfazl Rad, Julia Doll, Michaela A H Hofrichter, Asuman Koparir,[...]. Hum Genet 2021
1

Frequency and management of medically actionable incidental findings from genome and exome sequencing data: a systematic review.
Amal Elfatih, Idris Mohammed, Doua Abdelrahman, Borbala Mifsud. Physiol Genomics 2021
0

Interpretation of Incidental Genetic Findings Localizing to Genes Associated With Cardiac Channelopathies and Cardiomyopathies.
Jordan E Ezekian, Catherine Rehder, Priya S Kishnani, Andrew P Landstrom. Circ Genom Precis Med 2021
0

Beyond medically actionable results: an analytical pipeline for decreasing the burden of returning all clinically significant secondary findings.
Emma Reble, Mariana Gutierrez Salazar, Kathleen-Rose Zakoor, Sam Khalouei, Marc Clausen, Rita Kodida, Salma Shickh, Chloe Mighton, Iris Cohn, Kasmintan A Schrader,[...]. Hum Genet 2021
3

Next-generation sequencing for constitutional variants in the clinical laboratory, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG).
Catherine Rehder, Lora J H Bean, David Bick, Elizabeth Chao, Wendy Chung, Soma Das, Julianne O'Daniel, Heidi Rehm, Vandana Shashi, Lisa M Vincent. Genet Med 2021
4

Exome variant discrepancies due to reference-genome differences.
He Li, Moez Dawood, Michael M Khayat, Jesse R Farek, Shalini N Jhangiani, Ziad M Khan, Tadahiro Mitani, Zeynep Coban-Akdemir, James R Lupski, Eric Venner,[...]. Am J Hum Genet 2021
1


Considerations for whole exome sequencing unique to prenatal care.
Ahmad Abou Tayoun, Heather Mason-Suares. Hum Genet 2020
6