A citation-based method for searching scientific literature

David J Seiffert, Patricia McCarthy Veach, Bonnie LeRoy, Weihua Guan, Heather Zierhut. J Genet Couns 2019
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Experience with Parent Follow-Up for Communication Outcomes after Newborn Screening Identifies Carrier Status.
Michael H Farrell, Alison La Pean Kirschner, Audrey Tluczek, Philip M Farrell. J Pediatr 2020
8
50

Secondary findings: How did we get here, and where are we going?
Kelly E Ormond, Julianne M O'Daniel, Sarah S Kalia. J Genet Couns 2019
17
50

Prophylaxis with oral penicillin in children with sickle cell anemia. A randomized trial.
M H Gaston, J I Verter, G Woods, C Pegelow, J Kelleher, G Presbury, H Zarkowsky, E Vichinsky, R Iyer, J S Lobel. N Engl J Med 1986
811
50

Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens.
M Chillón, T Casals, B Mercier, L Bassas, W Lissens, S Silber, M C Romey, J Ruiz-Romero, C Verlingue, M Claustres. N Engl J Med 1995
713
50

Is public health ready for genetics?
N Holtzman. Arch Pediatr Adolesc Med 2001
8
50

Sickle cell trait as a contributory cause of death in natural disease.
Varsha Podduturi, Joseph M Guileyardo. J Forensic Sci 2015
4
50

Thirty-year risk of ischemic stroke in individuals with sickle cell trait and modification by chronic kidney disease: The atherosclerosis risk in communities (ARIC) study.
Melissa C Caughey, Vimal K Derebail, Nigel S Key, Alexander P Reiner, Rebecca F Gottesman, Abhijit V Kshirsagar, Gerardo Heiss. Am J Hematol 2019
5
50

Sickle cell trait diagnosis: clinical and social implications.
Rakhi P Naik, Carlton Haywood. Hematology Am Soc Hematol Educ Program 2015
54
50

Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project.
Tamara S Roman, Stephanie B Crowley, Myra I Roche, Ann Katherine M Foreman, Julianne M O'Daniel, Bryce A Seifert, Kristy Lee, Alicia Brandt, Chelsea Gustafson, Daniela M DeCristo,[...]. Am J Hum Genet 2020
5
50

Newborn blood spot screening for cystic fibrosis with a four-step screening strategy in the Netherlands.
Jeannette E Dankert-Roelse, Marelle J Bouva, Bernadette S Jakobs, Hettie M Janssens, Karin M de Winter-de Groot, Yvonne Schönbeck, Johan J P Gille, Vincent A M Gulmans, Rendelien K Verschoof-Puite, Peter C J I Schielen,[...]. J Cyst Fibros 2019
17
50


A Case for Inclusion of Genetic Counselors in Cardiac Care.
Patricia Arscott, Colleen Caleshu, Katrina Kotzer, Sarah Kreykes, Teresa Kruisselbrink, Kate Orland, Christina Rigelsky, Emily Smith, Katherine Spoonamore, Joy Larsen Haidle,[...]. Cardiol Rev 2016
21
50

The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5 year follow-up.
Martin H Steinberg, William F McCarthy, Oswaldo Castro, Samir K Ballas, F Danny Armstrong, Wally Smith, Kenneth Ataga, Paul Swerdlow, Abdullah Kutlar, Laura DeCastro,[...]. Am J Hematol 2010
301
50

Hormonal phenotype and HLA-genotype in families of patients with congenital adrenal hyperplasia (21-hydroxylase deficiency).
F Lorenzen, S Pang, M I New, B Dupont, M Pollack, D M Chow, L S Levine. Pediatr Res 1979
45
50

Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel.
Michael S Watson, Garry R Cutting, Robert J Desnick, Deborah A Driscoll, Katherine Klinger, Michael Mennuti, Glenn E Palomaki, Bradley W Popovich, Victoria M Pratt, Elizabeth M Rohlfs,[...]. Genet Med 2004
277
50

Association of sickle cell trait with chronic kidney disease and albuminuria in African Americans.
Rakhi P Naik, Vimal K Derebail, Morgan E Grams, Nora Franceschini, Paul L Auer, Gina M Peloso, Bessie A Young, Guillaume Lettre, Carmen A Peralta, Ronit Katz,[...]. JAMA 2014
101
50

Perspectives and Practices of Athletic Trainers and Team Physicians Implementing the 2010 NCAA Sickle Cell Trait Screening Policy.
Mary Anne McDonald, Melissa S Creary, Jill Powell, Lori-Ann Daley, Charlotte Baker, Charmaine Dm Royal. J Genet Couns 2017
4
50

Are heterocygotes for classical homocystinuria at risk of vitamin B12 and folic acid deficiency?
Mahmoud F Elsaid, Abdulbari Bener, Martin Lindner, Mahmoud Alzyoud, Noora Shahbek, Mohammed O Abdelrahman, Ghassan Abdoh, Mohammed S Bessisso, Johannes Zschocke, Georg F Hoffmann. Mol Genet Metab 2007
5
50

Fuel utilization in subjects with carnitine palmitoyltransferase 2 gene mutations.
Mette C Ørngreen, Morten Dunø, Rasmus Ejstrup, Ernst Christensen, Marianne Schwartz, Massimo Sacchetti, John Vissing. Ann Neurol 2005
61
50

Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene.
Patrick R Sosnay, Karen R Siklosi, Fredrick Van Goor, Kyle Kaniecki, Haihui Yu, Neeraj Sharma, Anabela S Ramalho, Margarida D Amaral, Ruslan Dorfman, Julian Zielenski,[...]. Nat Genet 2013
361
50

Cystic fibrosis carriers have higher neonatal immunoreactive trypsinogen values than non-carriers.
Carlo Castellani, Luigi Picci, Maurizio Scarpa, Maria Cristina Dechecchi, Luisa Zanolla, Baroukh Maurice Assael, Franco Zacchello. Am J Med Genet A 2005
27
50

Genetic counseling and risk communication services of newborn screening programs.
M Farrell, L Certain, P Farrell. Arch Pediatr Adolesc Med 2001
53
50

The impact of cardiovascular genetic counseling on patient empowerment.
Hannah E Ison, Stephanie M Ware, Tae-Hwi Schwantes-An, Samantha Freeze, Lindsey Elmore, Katherine G Spoonamore. J Genet Couns 2019
12
50

History of Newborn Screening for Cystic Fibrosis-The Early Years.
Georges Travert, Mary Heeley, Anthony Heeley. Int J Neonatal Screen 2020
3
50


Recommendations for the classification of diseases as CFTR-related disorders.
C Bombieri, M Claustres, K De Boeck, N Derichs, J Dodge, E Girodon, I Sermet, M Schwarz, M Tzetis, M Wilschanski,[...]. J Cyst Fibros 2011
225
50


Newborn screening for sickle cell diseases in the United States: A review of data spanning 2 decades.
Bradford L Therrell, Michele A Lloyd-Puryear, James R Eckman, Marie Y Mann. Semin Perinatol 2015
52
50


X-linked diseases: susceptible females.
Barbara R Migeon. Genet Med 2020
20
50

Initial sequencing and analysis of the human genome.
E S Lander, L M Linton, B Birren, C Nusbaum, M C Zody, J Baldwin, K Devon, K Dewar, M Doyle, W FitzHugh,[...]. Nature 2001
50

Beyond the simplicity of Mendelian inheritance.
Joseph Schacherer. C R Biol 2016
14
50


Understanding the role of argininosuccinate lyase transcript variants in the clinical and biochemical variability of the urea cycle disorder argininosuccinic aciduria.
Liyan Hu, Amit V Pandey, Sandra Eggimann, Véronique Rüfenacht, Dorothea Möslinger, Jean-Marc Nuoffer, Johannes Häberle. J Biol Chem 2013
6
50

Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis.
Harriet Corvol, Scott M Blackman, Pierre-Yves Boëlle, Paul J Gallins, Rhonda G Pace, Jaclyn R Stonebraker, Frank J Accurso, Annick Clement, Joseph M Collaco, Hong Dang,[...]. Nat Commun 2015
160
50

FRAX and the assessment of fracture probability in men and women from the UK.
J A Kanis, O Johnell, A Oden, H Johansson, E McCloskey. Osteoporos Int 2008
50

Prevalence of CFTR mutations in hypertrypsinaemia detected through neonatal screening for cystic fibrosis.
V Scotet, M De Braekeleer, M P Audrézet, L Lodé, C Verlingue, I Quéré, B Mercier, I Duguépéroux, J P Codet, M P Moineau,[...]. Clin Genet 2001
25
50

Association of sickle cell trait with atrial fibrillation: The REGARDS cohort.
Daniel R Douce, Elsayed Z Soliman, Rakhi Naik, Hyacinth I Hyacinth, Mary Cushman, Cheryl A Winkler, George Howard, Ethan M Lange, Leslie A Lange, Marguerite R Irvin,[...]. J Electrocardiol 2019
3
50

A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report.
Robert Resta, Barbara Bowles Biesecker, Robin L Bennett, Sandra Blum, Susan Estabrooks Hahn, Michelle N Strecker, Janet L Williams. J Genet Couns 2006
375
50

Cystic Fibrosis Transmembrane Conductance Regulator-Related Metabolic Syndrome and Cystic Fibrosis Screen Positive, Inconclusive Diagnosis.
Clement L Ren, Drucy S Borowitz, Tanja Gonska, Michelle S Howenstine, Hara Levy, John Massie, Carlos Milla, Anne Munck, Kevin W Southern. J Pediatr 2017
55
50

Newborn screening for cystic fibrosis: Role of primary care providers in caring for infants with positive screening results.
June C Carroll, Robin Z Hayeems, Fiona A Miller, Carolyn J Barg, Yvonne Bombard, Pranesh Chakraborty, Beth K Potter, Jessica Peace Bytautas, Karen Tam, Louise Taylor,[...]. Can Fam Physician 2021
1
100


Abnormal distribution of CF delta F508 allele in azoospermic men with congenital aplasia of epididymis and vas deferens.
V Dumur, R Gervais, J M Rigot, J J Lafitte, S Manouvrier, J Biserte, E Mazeman, P Roussel. Lancet 1990
161
50

Cystic fibrosis carriers are at increased risk for a wide range of cystic fibrosis-related conditions.
Aaron C Miller, Alejandro P Comellas, Douglas B Hornick, David A Stoltz, Joseph E Cavanaugh, Alicia K Gerke, Michael J Welsh, Joseph Zabner, Philip M Polgreen. Proc Natl Acad Sci U S A 2020
32
50

Population-based newborn screening for genetic disorders when multiple mutation DNA testing is incorporated: a cystic fibrosis newborn screening model demonstrating increased sensitivity but more carrier detections.
Anne Marie Comeau, Richard B Parad, Henry L Dorkin, Mark Dovey, Robert Gerstle, Kenan Haver, Allen Lapey, Brian P O'Sullivan, David A Waltz, Robert G Zwerdling,[...]. Pediatrics 2004
105
50


Heterozygous carriers of classical homocystinuria tend to have higher fasting serum homocysteine concentrations than non-carriers in the presence of folate deficiency.
Yung-Hsiu Lu, Li-Mei Cheng, Yu-Hsiu Huang, Ming-Yu Lo, Tina Jui-Ting Wu, Hsiang-Yu Lin, Ting-Rong Hsu, Dau-Ming Niu. Clin Nutr 2015
2
50

Primary care physicians' attitudes regarding follow-up care for children with positive newborn screening results.
Alex R Kemper, Rebecca L Uren, Kathryn L Moseley, Sarah J Clark. Pediatrics 2006
58
50

Kidney Function Decline among Black Patients with Sickle Cell Trait and Sickle Cell Disease: An Observational Cohort Study.
Kabir O Olaniran, Andrew S Allegretti, Sophia H Zhao, Maureen M Achebe, Nwamaka D Eneanya, Ravi I Thadhani, Sagar U Nigwekar, Sahir Kalim. J Am Soc Nephrol 2020
15
50

Phenotype of children with inconclusive cystic fibrosis diagnosis after newborn screening.
Anne Munck, Aurélie Bourmaud, Gabriel Bellon, Paul Picq, Philip M Farrell. Pediatr Pulmonol 2020
18
50


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.