A citation-based method for searching scientific literature

Lindsay H Zetzsche, Katrina E Kotzer, Karen E Wain. J Genet Couns 2014
Times Cited: 15







List of co-cited articles
48 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity



Genetic counseling for families with inherited susceptibility to breast and ovarian cancer.
B B Biesecker, M Boehnke, K Calzone, D S Markel, J E Garber, F S Collins, B L Weber. JAMA 1993
249
6

Traditional roles in a non-traditional setting: genetic counseling in precision oncology.
Jessica N Everett, Shanna L Gustafson, Victoria M Raymond. J Genet Couns 2014
17
6


Mutations in IHH, encoding Indian hedgehog, cause brachydactyly type A-1.
B Gao, J Guo, C She, A Shu, M Yang, Z Tan, X Yang, S Guo, G Feng, L He. Nat Genet 2001
171
6

A mutation in Ihh that causes digit abnormalities alters its signalling capacity and range.
Bo Gao, Jianxin Hu, Sigmar Stricker, Martin Cheung, Gang Ma, Kit Fong Law, Florian Witte, James Briscoe, Stefan Mundlos, Lin He,[...]. Nature 2009
69
6

Genetic counseling: Growth of the profession and the professional.
Bonnie J Baty. Am J Med Genet C Semin Med Genet 2018
8
12

Genetic counseling globally: Where are we now?
Kelly E Ormond, Mercy Ygoña Laurino, Kristine Barlow-Stewart, Tina-Marié Wessels, Shelley Macaulay, Jehannine Austin, Anna Middleton. Am J Med Genet C Semin Med Genet 2018
44
6

History of medical genetics in China.
Shang-zhi Huang, Yi-zhi Gao. Beijing Da Xue Xue Bao Yi Xue Ban 2006
2
50

Recommendations for the integration of genomics into clinical practice.
Sarah Bowdin, Adel Gilbert, Emma Bedoukian, Christopher Carew, Margaret P Adam, John Belmont, Barbara Bernhardt, Leslie Biesecker, Hans T Bjornsson, Miriam Blitzer,[...]. Genet Med 2016
79
6


Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment.
J H Xia, C Y Liu, B S Tang, Q Pan, L Huang, H P Dai, B R Zhang, W Xie, D X Hu, D Zheng,[...]. Nat Genet 1998
323
6


Evolving Roles for Physicians and Genetic Counselors in Managing Complex Genetic Disorders.
Celeste A Shelton, David C Whitcomb. Clin Transl Gastroenterol 2015
14
7

Building the genetic counsellor profession in the United Kingdom: two decades of growth and development.
Heather Skirton, Lauren Kerzin-Storrar, Chris Barnes, Georgina Hall, Mark Longmuir, Christine Patch, Gillian Scott, Jan Walford-Moore. J Genet Couns 2013
15
6

A Report on Ten Asia Pacific Countries on Current Status and Future Directions of the Genetic Counseling Profession: The Establishment of the Professional Society of Genetic Counselors in Asia.
Mercy Y Laurino, Kathleen A Leppig, Peter James Abad, Breana Cham, Yoyo Wing Yiu Chu, Saahil Kejriwal, Juliana M H Lee, Darci L Sternen, Jennifer K Thompson, Matthew J Burgess,[...]. J Genet Couns 2018
18
6

The novel gene locus for agenesis of permanent teeth (He-Zhao deficiency) maps to chromosome 10q11.2.
W Liu, H Wang, S Zhao, W Zhao, S Bai, Y Zhao, S Xu, C Wu, W Huang, Z Chen,[...]. J Dent Res 2001
23
6


Mutant ZP1 in familial infertility.
Hua-Lin Huang, Chao Lv, Ying-Chun Zhao, Wen Li, Xue-Mei He, Ping Li, Ai-Guo Sha, Xiao Tian, Christopher J Papasian, Hong-Wen Deng,[...]. N Engl J Med 2014
56
6

The role of genetic counsellors in genomic healthcare in the United Kingdom: a statement by the Association of Genetic Nurses and Counsellors.
Anna Middleton, Peter Marks, Anita Bruce, Liwsi K Protheroe-Davies, Cath King, Oonagh Claber, Catherine Houghton, Claire Giffney, Rhona Macleod, Claire Dolling,[...]. Eur J Hum Genet 2017
18
6

The rise of the genetic counseling profession in China.
Liya Sun, Bo Liang, Liping Zhu, Yiping Shen, Lin He. Am J Med Genet C Semin Med Genet 2019
7
14

KCNQ1 gain-of-function mutation in familial atrial fibrillation.
Yi-Han Chen, Shi-Jie Xu, Said Bendahhou, Xiao-Liang Wang, Ying Wang, Wen-Yuan Xu, Hong-Wei Jin, Hao Sun, Xiao-Yan Su, Qi-Nan Zhuang,[...]. Science 2003
688
6

The future is now: Technology's impact on the practice of genetic counseling.
Erynn S Gordon, Deepti Babu, Dawn A Laney. Am J Med Genet C Semin Med Genet 2018
18
6

Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students.
Megan E Grove, Shana White, Dianna G Fisk, Shannon Rego, Orit Dagan-Rosenfeld, Jennefer N Kohler, Chloe M Reuter, Devon Bonner, Matthew T Wheeler, Jonathan A Bernstein,[...]. J Genet Couns 2019
4
25

Cancer Genetic Counseling and Testing in an Era of Rapid Change.
Gillian W Hooker, Keelia Rhoads Clemens, John Quillin, Kristen J Vogel Postula, Pia Summerour, Rebecca Nagy, Adam H Buchanan. J Genet Couns 2017
24
6

Clinical Cardiovascular Genetic Counselors Take a Leading Role in Team-based Variant Classification.
Chloe Reuter, Megan E Grove, Kate Orland, Katherine Spoonamore, Colleen Caleshu. J Genet Couns 2018
19
6

The Exome Clinic and the role of medical genetics expertise in the interpretation of exome sequencing results.
Dustin Baldridge, Jennifer Heeley, Marisa Vineyard, Linda Manwaring, Tomi L Toler, Emily Fassi, Elise Fiala, Sarah Brown, Charles W Goss, Marcia Willing,[...]. Genet Med 2017
47
6

Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice Guideline.
Ray E Hershberger, Michael M Givertz, Carolyn Y Ho, Daniel P Judge, Paul F Kantor, Kim L McBride, Ana Morales, Matthew R G Taylor, Matteo Vatta, Stephanie M Ware. J Card Fail 2018
122
6

ClinVar: improving access to variant interpretations and supporting evidence.
Melissa J Landrum, Jennifer M Lee, Mark Benson, Garth R Brown, Chen Chao, Shanmuga Chitipiralla, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Wonhee Jang,[...]. Nucleic Acids Res 2018
815
6

Care in Specialized Centers and Data Sharing Increase Agreement in Hypertrophic Cardiomyopathy Genetic Test Interpretation.
Aisha Furqan, Patricia Arscott, Francesca Girolami, Allison L Cirino, Michelle Michels, Sharlene M Day, Iacopo Olivotto, Carolyn Y Ho, Euan Ashley, Eric M Green,[...]. Circ Cardiovasc Genet 2017
28
6

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.
Helen V Firth, Shola M Richards, A Paul Bevan, Stephen Clayton, Manuel Corpas, Diana Rajan, Steven Van Vooren, Yves Moreau, Roger M Pettett, Nigel P Carter. Am J Hum Genet 2009
920
6

ClinGen--the Clinical Genome Resource.
Heidi L Rehm, Jonathan S Berg, Lisa D Brooks, Carlos D Bustamante, James P Evans, Melissa J Landrum, David H Ledbetter, Donna R Maglott, Christa Lese Martin, Robert L Nussbaum,[...]. N Engl J Med 2015
482
6

Clinically impactful differences in variant interpretation between clinicians and testing laboratories: a single-center experience.
Austin Bland, Elizabeth A Harrington, Kyla Dunn, Mitchel Pariani, Julia C K Platt, Megan E Grove, Colleen Caleshu. Genet Med 2018
25
6

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
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,[...]. Am J Hum Genet 2010
6

Laboratory considerations for prenatal genetic testing.
Karen Wou, Wendy K Chung, Ronald J Wapner. Semin Perinatol 2018
3
33

A preliminary investigation of genetic counselors' information needs when receiving a variant of uncertain significance result: a mixed methods study.
Courtney L Scherr, Noralane M Lindor, Teri L Malo, Fergus J Couch, Susan T Vadaparampil. Genet Med 2015
18
6

The value of genomic variant ClinVar submissions from clinical providers: Beyond the addition of novel variants.
Karen E Wain, Emily Palen, Juliann M Savatt, Devin Shuman, Brenda Finucane, Andrea Seeley, Thomas D Challman, Scott M Myers, Christa Lese Martin. Hum Mutat 2018
5
20



Managing Variant Interpretation Discrepancies in Hereditary Cancer: Clinical Practice, Concerns, and Desired Resources.
Ellen Zirkelbach, Syed Hashmi, Aarti Ramdaney, Leslie Dunnington, Myla Ashfaq, Elizabeth K Nugent, Kate Wilson. J Genet Couns 2018
6
16

Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions.
Kelly D Farwell, Layla Shahmirzadi, Dima El-Khechen, Zöe Powis, Elizabeth C Chao, Brigette Tippin Davis, Ruth M Baxter, Wenqi Zeng, Cameron Mroske, Melissa C Parra,[...]. Genet Med 2015
285
6

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
513
6

Clinical laboratories collaborate to resolve differences in variant interpretations submitted to ClinVar.
Steven M Harrison, Jill S Dolinsky, Amy E Knight Johnson, Tina Pesaran, Danielle R Azzariti, Sherri Bale, Elizabeth C Chao, Soma Das, Lisa Vincent, Heidi L Rehm. Genet Med 2017
116
6

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
6

Genetics in health practice and education special issue.
Clara L Gaff, Janet K D Williams, Joseph D McInerney. J Genet Couns 2008
4
25

Genetic counselors on the frontline of precision health.
Michael J Bamshad, Pilar L Magoulas, Karin M Dent. Am J Med Genet C Semin Med Genet 2018
6
16




Interactive genetic counseling role-play: a novel educational strategy for family physicians.
Sean M Blaine, June C Carroll, Andrea L Rideout, Gord Glendon, Wendy Meschino, Cheryl Shuman, Deanna Telner, Natasha Van Iderstine, Joanne Permaul. J Genet Couns 2008
12
8


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.