A citation-based method for searching scientific literature

David Dimmock. Curr Protoc Hum Genet 2013
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
50

Exploring concordance and discordance for return of incidental findings from clinical sequencing.
Robert C Green, Jonathan S Berg, Gerard T Berry, Leslie G Biesecker, David P Dimmock, James P Evans, Wayne W Grody, Madhuri R Hegde, Sarah Kalia, Bruce R Korf,[...]. Genet Med 2012
122
33


Point-counterpoint. Ethics and genomic incidental findings.
Amy L McGuire, Steven Joffe, Barbara A Koenig, Barbara B Biesecker, Laurence B McCullough, Jennifer S Blumenthal-Barby, Timothy Caulfield, Sharon F Terry, Robert C Green. Science 2013
128
33


Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
33

What can exome sequencing do for you?
Jacek Majewski, Jeremy Schwartzentruber, Emilie Lalonde, Alexandre Montpetit, Nada Jabado. J Med Genet 2011
209
33


Next generation sequencing in the clinical domain: clinical advantages, practical, and ethical challenges.
Rose Thompson, Cheney J G Drew, Rhys H Thomas. Adv Protein Chem Struct Biol 2012
19
33

Attitudes of Canadian researchers toward the return to participants of incidental and targeted genomic findings obtained in a pediatric research setting.
Conrad V Fernandez, Caron Strahlendorf, Denise Avard, Bartha M Knoppers, Colleen O'Connell, Eric Bouffet, David Malkin, Nada Jabado, Kym Boycott, Poul H Sorensen. Genet Med 2013
35
16


Incidental findings in trauma patients: dedicated communication with the primary care physician ensures adequate follow-up.
D Dante Yeh, Ayesha M Imam, Shani H Truong, Erin L McLaughlin, Eric N Klein, Laura L Avery, George C Velmahos. World J Surg 2013
13
16

Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur J Hum Genet 2013
203
16


Point-counterpoint. Patient autonomy and incidental findings in clinical genomics.
Susan M Wolf, George J Annas, Sherman Elias. Science 2013
158
16



Incidental findings in imaging research: evaluating incidence, benefit, and burden.
Nicholas M Orme, Joel G Fletcher, Hassan A Siddiki, W Scott Harmsen, Megan M O'Byrne, John D Port, William J Tremaine, Henry C Pitot, Elizabeth G McFarland, Marguerite E Robinson,[...]. Arch Intern Med 2010
107
16

Gender preference and awareness regarding sex determination among antenatal mothers attending a medical college of eastern India.
Shamima Yasmin, Anindya Mukherjee, Nirmalya Manna, Baijayanti Baur, Mousumi Datta, Manabendra Sau, Manidipa Roy, Samir Dasgupta. Scand J Public Health 2013
10
16



'Information is information': a public perspective on incidental findings in clinical and research genome-based testing.
S Daack-Hirsch, M Driessnack, A Hanish, V A Johnson, L L Shah, C M Simon, J K Williams. Clin Genet 2013
50
16

Recommendations for the predictive genetic test in Huntington's disease.
R MacLeod, A Tibben, M Frontali, G Evers-Kiebooms, A Jones, A Martinez-Descales, R A Roos. Clin Genet 2013
110
16

Incidental findings from clinical genome-wide sequencing: a review.
Z Lohn, S Adam, P H Birch, J M Friedman. J Genet Couns 2014
33
16


Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing.
George McGillivray, Jill A Rosenfeld, R J McKinlay Gardner, Lynn H Gillam. Prenat Diagn 2012
68
16

Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes.
Jennifer J Johnston, Wendy S Rubinstein, Flavia M Facio, David Ng, Larry N Singh, Jamie K Teer, James C Mullikin, Leslie G Biesecker. Am J Hum Genet 2012
159
16


Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent.
Wybo Dondorp, Birgit Sikkema-Raddatz, Christine de Die-Smulders, Guido de Wert. Hum Mutat 2012
47
16


Personal genome research : what should the participant be told?
Amy L McGuire, James R Lupski. Trends Genet 2010
54
16

Predictive and preimplantation genetic testing for Huntington's disease and other late onset dominant disorders: not in conflict but complementary.
G Evers-Kiebooms, J P Fryns, K Demyttenaere, M Decruyenaere, A Boogaerts, T Cloostermans, J J Cassiman, R Dom, H Van den Berghe. Clin Genet 1996
11
16

Paediatric research and the communication of not-so incidental findings.
Bartha Maria Knoppers. Paediatr Child Health 2012
15
16

Parental decisions following prenatal diagnosis of sex chromosome aneuploidy: a trend over time.
S M Christian, D Koehn, R Pillay, A MacDougall, R D Wilson. Prenat Diagn 2000
45
16

Growth hormone receptor and serum binding protein: purification, cloning and expression.
D W Leung, S A Spencer, G Cachianes, R G Hammonds, C Collins, W J Henzel, R Barnard, M J Waters, W I Wood. Nature 1987
16


Evaluation of a district growth screening programme: the Oxford Growth Study.
M L Ahmed, A D Allen, A Sharma, J A Macfarlane, D B Dunger. Arch Dis Child 1993
44
16

Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutation.
Ofer Sarig, Sagi Nahum, Debora Rapaport, Akemi Ishida-Yamamoto, Dana Fuchs-Telem, Li Qiaoli, Ksenya Cohen-Katsenelson, Ronen Spiegel, Janna Nousbeck, Shirli Israeli,[...]. Am J Hum Genet 2012
43
16

A common polymorphism of the growth hormone receptor is associated with increased responsiveness to growth hormone.
Christine Dos Santos, Laurent Essioux, Cécile Teinturier, Maïté Tauber, Vincent Goffin, Pierre Bougnères. Nat Genet 2004
235
16


Effects of heterozygosity for the E180 splice mutation causing growth hormone receptor deficiency in Ecuador on IGF-I, IGFBP-3, and stature.
Jaime Guevara-Aguirre, Arlan L Rosenbloom, Marco Guevara-Aguirre, Kemal Yariz, Jeanette Saavedra, Lisa Baumbach, Jonathan Shuster. Growth Horm IGF Res 2007
10
16

The missing "link": an autosomal recessive short stature syndrome caused by a hypofunctional XYLT1 mutation.
Julia Schreml, Burak Durmaz, Ozgur Cogulu, Katharina Keupp, Filippo Beleggia, Esther Pohl, Esther Milz, Mahmut Coker, Sema Kalkan Ucar, Gudrun Nürnberg,[...]. Hum Genet 2014
44
16

Evidence for a continuum of genetic, phenotypic, and biochemical abnormalities in children with growth hormone insensitivity.
Alessia David, Vivian Hwa, Louise A Metherell, Irène Netchine, Cecilia Camacho-Hübner, Adrian J L Clark, Ron G Rosenfeld, Martin O Savage. Endocr Rev 2011
122
16

Large-scale pooled next-generation sequencing of 1077 genes to identify genetic causes of short stature.
Sophie R Wang, Heather Carmichael, Shayne F Andrew, Timothy C Miller, Jennifer E Moon, Michael A Derr, Vivian Hwa, Joel N Hirschhorn, Andrew Dauber. J Clin Endocrinol Metab 2013
45
16

Novel microcephalic primordial dwarfism disorder associated with variants in the centrosomal protein ninein.
Andrew Dauber, Stephen H Lafranchi, Zoltan Maliga, Julian C Lui, Jennifer E Moon, Cailin McDeed, Katrin Henke, Jonathan Zonana, Garrett A Kingman, Tune H Pers,[...]. J Clin Endocrinol Metab 2012
41
16

Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Hana Lango Allen, Karol Estrada, Guillaume Lettre, Sonja I Berndt, Michael N Weedon, Fernando Rivadeneira, Cristen J Willer, Anne U Jackson, Sailaja Vedantam, Soumya Raychaudhuri,[...]. Nature 2010
16

Low incidence of pathology detection and high cost of screening in the evaluation of asymptomatic short children.
Stephanie Sisley, Marcela Vargas Trujillo, Jane Khoury, Philippe Backeljauw. J Pediatr 2013
47
16

Idiopathic short stature: management and growth hormone treatment.
J M Wit, E O Reiter, J L Ross, P H Saenger, M O Savage, A D Rogol, P Cohen. Growth Horm IGF Res 2008
46
16

Mutations in PIK3R1 cause SHORT syndrome.
David A Dyment, Amanda C Smith, Diana Alcantara, Jeremy A Schwartzentruber, Lina Basel-Vanagaite, Cynthia J Curry, I Karen Temple, William Reardon, Sahar Mansour, Mushfequr R Haq,[...]. Am J Hum Genet 2013
106
16

Reduced concentration of serum growth hormone-binding protein in children with idiopathic short stature. National Cooperative Growth Study.
L M Carlsson, K M Attie, P G Compton, R V Vitangcol, T J Merimee. J Clin Endocrinol Metab 1994
88
16


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.