A citation-based method for searching scientific literature

Allison Werner-Lin, Frances K Barg, Katherine S Kellom, Kallyn J Stumm, Lisa Pilchman, Ashley N Tomlinson, Barbara A Bernhardt. Qual Health Res 2016
Times Cited: 25







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



Times Cited
  Times     Co-cited
Similarity


Women's experiences receiving abnormal prenatal chromosomal microarray testing results.
Barbara A Bernhardt, Danielle Soucier, Karen Hanson, Melissa S Savage, Laird Jackson, Ronald J Wapner. Genet Med 2013
129
68

"Something Extra on Chromosome 5": Parents' Understanding of Positive Prenatal Chromosomal Microarray Analysis (CMA) Results.
Sarah A Walser, Allison Werner-Lin, Amita Russell, Ronald J Wapner, Barbara A Bernhardt. J Genet Couns 2016
18
66

Chromosomal microarray versus karyotyping for prenatal diagnosis.
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N Engl J Med 2012
643
44

Comparing genetic counselor's and patient's perceptions of needs in prenatal chromosomal microarray testing.
Sarah A Walser, Katherine S Kellom, Steven C Palmer, Barbara A Bernhardt. Prenat Diagn 2015
25
32

An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing.
Barbara A Bernhardt, Katherine Kellom, Alexandra Barbarese, W Andrew Faucett, Ronald J Wapner. J Genet Couns 2014
37
28


"If it helps..." the use of microarray technology in prenatal testing: patient and partners reflections.
Sarah C Hillman, John Skelton, Elizabeth Quinlan-Jones, Amie Wilson, Mark D Kilby. Am J Med Genet A 2013
26
24

The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents' Experiences.
S L van der Steen, S R Riedijk, J Verhagen-Visser, L C P Govaerts, M I Srebniak, D Van Opstal, M Joosten, M F C M Knapen, A Tibben, K E M Diderich,[...]. J Genet Couns 2016
26
24



"What does it mean?": uncertainties in understanding results of chromosomal microarray testing.
Marian Reiff, Barbara A Bernhardt, Surabhi Mulchandani, Danielle Soucier, Diana Cornell, Reed E Pyeritz, Nancy B Spinner. Genet Med 2012
75
16

Prenatal chromosomal microarray analysis: a survey of prenatal genetic counselors' experiences and attitudes.
Marina Mikhaelian, Patricia McCarthy Veach, Ian MacFarlane, Bonnie S LeRoy, Matthew Bower. Prenat Diagn 2013
18
22

Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testing.
S L van der Steen, K E M Diderich, S R Riedijk, J Verhagen-Visser, L C P Govaerts, M Joosten, M F C M Knapen, D Van Opstal, M I Srebniak, A Tibben,[...]. Clin Genet 2015
32
16

What results to disclose, when, and who decides? Healthcare professionals' views on prenatal chromosomal microarray analysis.
Shiri Shkedi-Rafid, Angela Fenwick, Sandi Dheensa, Diana Wellesley, Anneke M Lucassen. Prenat Diagn 2016
20
20

Balancing Genetics (Science) and Counseling (Art) in Prenatal Chromosomal Microarray Testing.
Allison Werner-Lin, Judith L M McCoyd, Barbara A Bernhardt. J Genet Couns 2016
14
28

Promises, pitfalls and practicalities of prenatal whole exome sequencing.
Sunayna Best, Karen Wou, Neeta Vora, Ignatia B Van der Veyver, Ronald Wapner, Lyn S Chitty. Prenat Diagn 2018
130
16

"It's probably nothing, but…" Couples' experiences of pregnancy following an uncertain prenatal genetic result.
Stina Lou, Kirsten Lomborg, Celine Lewis, Sam Riedijk, Olav Bjørn Petersen, Ida Vogel. Acta Obstet Gynecol Scand 2020
6
66



Unexpected diagnosis of fetal abnormality: women's encounters with caregivers.
Joan G Lalor, Declan Devane, Cecily M Begley. Birth 2007
91
12

The decision to continue: the experiences and needs of parents who receive a prenatal diagnosis of holoprosencephaly.
Krista Redlinger-Grosse, Barbara A Bernhardt, Kate Berg, Maximilian Muenke, Barbara B Biesecker. Am J Med Genet 2002
49
12

Preparing Heart and Mind for Becoming a Parent Following a Diagnosis of Fetal Anomaly.
Anne Chevalier McKechnie, Karen Pridham, Audrey Tluczek. Qual Health Res 2015
14
21

Prenatal whole-exome sequencing: parental attitudes.
Eve J Kalynchuk, Andrew Althouse, Lisa S Parker, Devereux N Saller, Aleksandar Rajkovic. Prenat Diagn 2015
32
12


Embodied experiences of prenatal diagnosis of fetal abnormality and pregnancy termination.
Penelope Pitt, Belinda J McClaren, Jan Hodgson. Reprod Health Matters 2016
9
33

Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics.
Anthony R Gregg, Brian G Skotko, Judith L Benkendorf, Kristin G Monaghan, Komal Bajaj, Robert G Best, Susan Klugman, Michael S Watson. Genet Med 2016
294
12

Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.
S C Hillman, D J McMullan, G Hall, F S Togneri, N James, E J Maher, C H Meller, D Williams, R J Wapner, E R Maher,[...]. Ultrasound Obstet Gynecol 2013
154
12

Exome sequencing positively identified relevant alterations in more than half of cases with an indication of prenatal ultrasound anomalies.
Christina L Alamillo, Zöe Powis, Kelly Farwell, Layla Shahmirzadi, Elaine C Weltmer, John Turocy, Thomas Lowe, Christine Kobelka, Emily Chen, Donald Basel,[...]. Prenat Diagn 2015
54
12


Monitoring the prenatal detection of structural fetal congenital anomalies in England and Wales: register-based study.
Patricia A Boyd, Ann M Tonks, Judith Rankin, Catherine Rounding, Diana Wellesley, Elizabeth S Draper. J Med Screen 2011
35
12

Prenatal whole exome sequencing: the views of clinicians, scientists, genetic counsellors and patient representatives.
Elizabeth Quinlan-Jones, Mark D Kilby, Sheila Greenfield, Michael Parker, Dominic McMullan, Matthew E Hurles, Sarah C Hillman. Prenat Diagn 2016
27
12

Parental perceptions of prenatal whole exome sequencing (PPPWES) study.
Karen Wou, Talia Weitz, Clare McCormack, Julia Wynn, Erica Spiegel, Jessica Giordano, Ronald J Wapner, Wendy K Chung. Prenat Diagn 2018
11
27


Ethical considerations in prenatal testing: Genomic testing and medical uncertainty.
Anastasia Richardson, Kelly E Ormond. Semin Fetal Neonatal Med 2018
13
23

Impacts of variants of uncertain significance on parental perceptions of children after prenatal chromosome microarray testing.
Preeya Desai, Hannah Haber, Jessica Bulafka, Amita Russell, Rebecca Clifton, Julia Zachary, Seonjoo Lee, Tianshu Feng, Ronald Wapner, Catherine Monk,[...]. Prenat Diagn 2018
16
18

Parental experiences of prenatal whole exome sequencing (WES) in cases of ultrasound diagnosed fetal structural anomaly.
Elizabeth Quinlan-Jones, Sarah C Hillman, Mark D Kilby, Sheila M Greenfield. Prenat Diagn 2017
14
21

Parent's experiences of counselling and their need for support following a prenatal diagnosis of congenital heart disease--a qualitative study in a Swedish context.
Ewa-Lena Bratt, Stina Järvholm, Britt-Marie Ekman-Joelsson, Lars-Åke Mattson, Mats Mellander. BMC Pregnancy Childbirth 2015
44
12

Copy number variants, aneuploidies, and human disease.
Christa Lese Martin, Brianne E Kirkpatrick, David H Ledbetter. Clin Perinatol 2015
33
8

Internet use in pregnancy informs women's decision making: a web-based survey.
Briege M Lagan, Marlene Sinclair, W George Kernohan. Birth 2010
188
8

Parents' Perspectives on Variants of Uncertain Significance from Chromosome Microarray Analysis.
Lesli A Kiedrowski, Kailey M Owens, Beverly M Yashar, Jane L Schuette. J Genet Couns 2016
28
8

The travesty of choosing after positive prenatal diagnosis.
Margarete Sandelowski, Julie Barroso. J Obstet Gynecol Neonatal Nurs 2005
86
8

Shift happens: family background influences clinical variability in genetic neurodevelopmental disorders.
Brenda Finucane, Thomas D Challman, Christa Lese Martin, David H Ledbetter. Genet Med 2016
24
8


The influence of experiential knowledge on prenatal screening and testing decisions.
Holly Etchegary, Beth Potter, Heather Howley, Mario Cappelli, Doug Coyle, Ian Graham, Mark Walker, Brenda Wilson. Genet Test 2008
50
8

Prenatal diagnosis of fetal abnormality: psychological effects on women in low-risk pregnancies.
H Statham, W Solomou, L Chitty. Baillieres Best Pract Res Clin Obstet Gynaecol 2000
72
8

Women's views of pregnancy ultrasound: a systematic review.
Jo Garcia, Leanne Bricker, Jane Henderson, Marie-Anne Martin, Miranda Mugford, Jim Nielson, Tracy Roberts. Birth 2002
144
8

"Testing times, challenging choices": an Australian study of prenatal genetic counseling.
Jan M Hodgson, Lynn H Gillam, Margaret A Sahhar, Sylvia A Metcalfe. J Genet Couns 2010
26
8

Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis.
M M Gil, M S Quezada, R Revello, R Akolekar, K H Nicolaides. Ultrasound Obstet Gynecol 2015
294
8


Patients-in-waiting: Living between sickness and health in the genomics era.
Stefan Timmermans, Mara Buchbinder. J Health Soc Behav 2010
137
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.