A citation-based method for searching scientific literature

Samantha N Hartin, Waheeda A Hossain, Nicolette Weisensel, Merlin G Butler. Am J Med Genet A 2018
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


Molecular genetic classification in Prader-Willi syndrome: a multisite cohort study.
Merlin G Butler, Samantha N Hartin, Waheeda A Hossain, Ann M Manzardo, Virginia Kimonis, Elisabeth Dykens, June Anne Gold, Soo-Jeong Kim, Nicolette Weisensel, Roy Tamura,[...]. J Med Genet 2019
48
54

Analysis of the Prader-Willi syndrome imprinting center using droplet digital PCR and next-generation whole-exome sequencing.
Samantha N Hartin, Waheeda A Hossain, David Francis, David E Godler, Sangjucta Barkataki, Merlin G Butler. Mol Genet Genomic Med 2019
10
50

Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster.
Trilochan Sahoo, Daniela del Gaudio, Jennifer R German, Marwan Shinawi, Sarika U Peters, Richard E Person, Adolfo Garnica, Sau Wai Cheung, Arthur L Beaudet. Nat Genet 2008
374
36

Prader-Willi syndrome.
Suzanne B Cassidy, Stuart Schwartz, Jennifer L Miller, Daniel J Driscoll. Genet Med 2012
631
36


Single Gene and Syndromic Causes of Obesity: Illustrative Examples.
Merlin G Butler. Prog Mol Biol Transl Sci 2016
28
36

Prader-Willi syndrome: consensus diagnostic criteria.
V A Holm, S B Cassidy, M G Butler, J M Hanchett, L R Greenswag, B Y Whitman, F Greenberg. Pediatrics 1993
869
36

Methylation-specific multiplex ligation-dependent probe amplification and identification of deletion genetic subtypes in Prader-Willi syndrome.
Rebecca S Henkhaus, Soo-Jeong Kim, Virginia E Kimonis, June-Anne Gold, Elisabeth M Dykens, Daniel J Driscoll, Merlin G Butler. Genet Test Mol Biomarkers 2012
23
27

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.
R D Nicholls, J H Knoll, M G Butler, S Karam, M Lalande. Nature 1989
661
27


Imprinting-mutation mechanisms in Prader-Willi syndrome.
T Ohta, T A Gray, P K Rogan, K Buiting, J M Gabriel, S Saitoh, B Muralidhar, B Bilienska, M Krajewska-Walasek, D J Driscoll,[...]. Am J Hum Genet 1999
186
27

Epimutations in Prader-Willi and Angelman syndromes: a molecular study of 136 patients with an imprinting defect.
Karin Buiting, Stephanie Gross, Christina Lich, Gabriele Gillessen-Kaesbach, Osman el-Maarri, Bernhard Horsthemke. Am J Hum Genet 2003
180
27

Prader-Willi syndrome.
Suzanne B Cassidy, Daniel J Driscoll. Eur J Hum Genet 2009
341
27

Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy.
S B Cassidy, L W Lai, R P Erickson, L Magnuson, E Thomas, R Gendron, J Herrmann. Am J Hum Genet 1992
145
27

Practice guidelines for the molecular analysis of Prader-Willi and Angelman syndromes.
Simon C Ramsden, Jill Clayton-Smith, Rachael Birch, Karin Buiting. BMC Med Genet 2010
61
27

The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria.
M Gunay-Aygun, S Schwartz, S Heeger, M A O'Riordan, S B Cassidy. Pediatrics 2001
262
27


Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy.
Merlin G Butler, Douglas C Bittel, Nataliya Kibiryeva, Zohreh Talebizadeh, Travis Thompson. Pediatrics 2004
174
27

Prader-Willi-Like Phenotype Caused by an Atypical 15q11.2 Microdeletion.
Qiming Tan, Kathryn J Potter, Lisa Cole Burnett, Camila E Orsso, Mark Inman, Davis C Ryman, Andrea M Haqq. Genes (Basel) 2020
13
27


Molecular basis of obesity: current status and future prospects.
Hélène Choquet, David Meyre. Curr Genomics 2011
61
18

Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism.
Christian P Schaaf, Manuel L Gonzalez-Garay, Fan Xia, Lorraine Potocki, Karen W Gripp, Baili Zhang, Brock A Peters, Mark A McElwain, Radoje Drmanac, Arthur L Beaudet,[...]. Nat Genet 2013
167
18

PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
18

Detailed phenotype-genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader-Willi-like phenotype.
Maria Clara Bonaglia, Roberto Ciccone, Giorgio Gimelli, Stefania Gimelli, Susan Marelli, Joke Verheij, Roberto Giorda, Rita Grasso, Renato Borgatti, Filomena Pagone,[...]. Eur J Hum Genet 2008
57
18

A systematic review of genetic syndromes with obesity.
Y Kaur, R J de Souza, W T Gibson, D Meyre. Obes Rev 2017
69
18


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
18

Genetic basis of Prader-Willi syndrome in Korea: less uniparental disomy than has been recognized?
H-J Kim, H-J Cho, D-K Jin, E-K Kwon, C-S Ki, J-W Kim, S-H Kim. Clin Genet 2004
10
20

The relationship between compulsive behaviour and academic achievement across the three genetic subtypes of Prader-Willi syndrome.
J Zarcone, D Napolitano, C Peterson, J Breidbord, S Ferraioli, M Caruso-Anderson, L Holsen, M G Butler, T Thompson. J Intellect Disabil Res 2007
41
18

UPD detection using homozygosity profiling with a SNP genotyping microarray.
Peter Papenhausen, Stuart Schwartz, Hiba Risheg, Elisabeth Keitges, Inder Gadi, Rachel D Burnside, Vikram Jaswaney, John Pappas, Romela Pasion, Kenneth Friedman,[...]. Am J Med Genet A 2011
88
18

Prader-Willi syndrome genetic subtypes and clinical neuropsychiatric diagnoses in residential care adults.
A M Manzardo, N Weisensel, S Ayala, W Hossain, M G Butler. Clin Genet 2018
13
18

Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.
Douglas C Bittel, Merlin G Butler. Expert Rev Mol Med 2005
182
18



Prader-Willi Syndrome: Clinical and Genetic Findings.
Merlin G Butler, Travis Thompson. Endocrinologist 2000
61
18

Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.
D H Ledbetter, V M Riccardi, S D Airhart, R J Strobel, B S Keenan, J D Crawford. N Engl J Med 1981
488
18

Nutritional phases in Prader-Willi syndrome.
Jennifer L Miller, Christy H Lynn, Danielle C Driscoll, Anthony P Goldstone, June-Anne Gold, Virginia Kimonis, Elisabeth Dykens, Merlin G Butler, Jonathan J Shuster, Daniel J Driscoll. Am J Med Genet A 2011
200
18

Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypes.
Soo-Jeong Kim, Jennifer L Miller, Paul J Kuipers, Jennifer Ruth German, Arthur L Beaudet, Trilochan Sahoo, Daniel J Driscoll. Eur J Hum Genet 2012
62
18

Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes.
E Roof, W Stone, W MacLean, I D Feurer, T Thompson, M G Butler. J Intellect Disabil Res 2000
111
18

X-chromosome inactivation patterns in females with Prader-Willi syndrome.
Merlin G Butler, Mariana F Theodoro, Douglas C Bittel, Paul J Kuipers, Daniel J Driscoll, Zohreh Talebizadeh. Am J Med Genet A 2007
15
18

Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.
M A Angulo, M G Butler, M E Cataletto. J Endocrinol Invest 2015
235
18

Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy.
Harm Boer, Anthony Holland, Joyce Whittington, Jill Butler, Tessa Webb, David Clarke. Lancet 2002
176
18

Clinical and genetic aspects of Angelman syndrome.
Charles A Williams, Daniel J Driscoll, Aditi I Dagli. Genet Med 2010
164
18



Prader-Willi Syndrome - Clinical Genetics, Diagnosis and Treatment Approaches: An Update.
Merlin G Butler, Jennifer L Miller, Janice L Forster. Curr Pediatr Rev 2019
50
18

Update of the EMQN/ACGS best practice guidelines for molecular analysis of Prader-Willi and Angelman syndromes.
Jasmin Beygo, Karin Buiting, Simon C Ramsden, Rachael Ellis, Jill Clayton-Smith, Deniz Kanber. Eur J Hum Genet 2019
14
18

The dilemma of diagnostic testing for Prader-Willi syndrome.
Arabella Smith, Dorothy Hung. Transl Pediatr 2017
10
20

New mutations in BBS genes in small consanguineous families with Bardet-Biedl syndrome: detection of candidate regions by homozygosity mapping.
Ines Pereiro, Diana Valverde, Teresa Piñeiro-Gallego, Montserrat Baiget, Salud Borrego, Carmen Ayuso, Charles Searby, Darryl Nishimura. Mol Vis 2010
28
9

New genetic loci link adipose and insulin biology to body fat distribution.
Dmitry Shungin, Thomas W Winkler, Damien C Croteau-Chonka, Teresa Ferreira, Adam E Locke, Reedik Mägi, Rona J Strawbridge, Tune H Pers, Krista Fischer, Anne E Justice,[...]. Nature 2015
747
9


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.