A citation-based method for searching scientific literature

Karin Salehi Karlslätt, Maria Pettersson, Nina Jäntti, Przemyslaw Szafranski, Tomas Wester, Britt Husberg, Ulla Ullberg, Pawel Stankiewicz, Ann Nordgren, Johanna Lundin, Anna Lindstrand, Agneta Nordenskjöld. Mol Genet Genomic Med 2019
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


Pathogenic copy number variants are detected in a subset of patients with gastrointestinal malformations.
Johanna Winberg, Peter Gustavsson, Ellika Sahlin, Magnus Larsson, Henrik Ehrén, Magdalena Fossum, Tomas Wester, Ann Nordgren, Agneta Nordenskjöld. Mol Genet Genomic Med 2020
1
100

Noncoding copy-number variations are associated with congenital limb malformation.
Ricarda Flöttmann, Bjørt K Kragesteen, Sinje Geuer, Magdalena Socha, Lila Allou, Anna Sowińska-Seidler, Laure Bosquillon de Jarcy, Johannes Wagner, Aleksander Jamsheer, Barbara Oehl-Jaschkowitz,[...]. Genet Med 2018
20
16

A fetus with de novo 2q33.2q35 deletion including MAP2 with brain anomalies, esophageal atresia, and laryngeal stenosis.
Ellen van Binsbergen, Richard J Ellis, Nadia Abdelmalik, Joanna Jarvis, Kashmir Randhawa, Josephine Wyatt-Ashmead, Natalie Canham, J Guy Thorpe-Beeston, Grazia M S Mancini, Mieke M Van Haelst. Am J Med Genet A 2014
7
16

Mutation of MEF2A in an inherited disorder with features of coronary artery disease.
Lejin Wang, Chun Fan, Sarah E Topol, Eric J Topol, Qing Wang. Science 2003
238
16

Partial tetrasomy 14 associated with multiple malformations.
Johanna Winberg, Kristina Lagerstedt Robinson, Karin Naess, Nicole Lesko, Rolf Wibom, Agne Liedén, Britt-Marie Anderlid, Caroline Graff, Agneta Nordenskjöld, Ann Nordgren,[...]. Am J Med Genet A 2013
4
25

Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidney.
Rik Westland, Miguel Verbitsky, Katarina Vukojevic, Brittany J Perry, David A Fasel, Petra J G Zwijnenburg, Arend Bökenkamp, Johan J P Gille, Mirna Saraga-Babic, Gian Marco Ghiggeri,[...]. Kidney Int 2015
42
16

Proteomics. Tissue-based map of the human proteome.
Mathias Uhlén, Linn Fagerberg, Björn M Hallström, Cecilia Lindskog, Per Oksvold, Adil Mardinoglu, Åsa Sivertsson, Caroline Kampf, Evelina Sjöstedt, Anna Asplund,[...]. Science 2015
16

Parental somatic mosaicism is underrecognized and influences recurrence risk of genomic disorders.
Ian M Campbell, Bo Yuan, Caroline Robberecht, Rolph Pfundt, Przemyslaw Szafranski, Meriel E McEntagart, Sandesh C S Nagamani, Ayelet Erez, Magdalena Bartnik, Barbara Wiśniowiecka-Kowalnik,[...]. Am J Hum Genet 2014
142
16

Chimerism resulting from parthenogenetic activation and dispermic fertilization.
Johanna Winberg, Peter Gustavsson, Kristina Lagerstedt-Robinson, Elisabeth Blennow, Johanna Lundin, Erik Iwarsson, Anna Nordenström, Britt-Marie Anderlid, Marie-Louise Bondeson, Agneta Nordenskjöld,[...]. Am J Med Genet A 2010
19
16

Systematic assessment of atypical deletions reveals genotype-phenotype correlation in 22q11.2.
A Rauch, S Zink, C Zweier, C T Thiel, A Koch, R Rauch, J Lascorz, U Hüffmeier, M Weyand, H Singer,[...]. J Med Genet 2005
108
16

Somatic mosaicism for copy number variation in differentiated human tissues.
Arkadiusz Piotrowski, Carl E G Bruder, Robin Andersson, Teresita Diaz de Ståhl, Uwe Menzel, Johanna Sandgren, Andrzej Poplawski, Desiree von Tell, Chiquito Crasto, Adam Bogdan,[...]. Hum Mutat 2008
151
16

Global variation in copy number in the human genome.
Richard Redon, Shumpei Ishikawa, Karen R Fitch, Lars Feuk, George H Perry, T Daniel Andrews, Heike Fiegler, Michael H Shapero, Andrew R Carson, Wenwei Chen,[...]. Nature 2006
16

De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association.
Alina Hilger, Charlotte Schramm, Tracie Pennimpede, Lars Wittler, Gabriel C Dworschak, Enrika Bartels, Hartmut Engels, Alexander M Zink, Franziska Degenhardt, Annette M Müller,[...]. Eur J Hum Genet 2013
30
16

Systematic analysis of copy number variation associated with congenital diaphragmatic hernia.
Qihui Zhu, Frances A High, Chengsheng Zhang, Eliza Cerveira, Meaghan K Russell, Mauro Longoni, Maliackal P Joy, Mallory Ryan, Adam Mil-Homens, Lauren Bellfy,[...]. Proc Natl Acad Sci U S A 2018
10
16

Loss of function in ROBO1 is associated with tetralogy of Fallot and septal defects.
Paul Kruszka, Pranoot Tanpaiboon, Katherine Neas, Kathleen Crosby, Seth I Berger, Ariel F Martinez, Yonit A Addissie, Yupada Pongprot, Rekwan Sittiwangkul, Suchaya Silvilairat,[...]. J Med Genet 2017
8
16

The inv dup (15) or idic (15) syndrome (Tetrasomy 15q).
Agatino Battaglia. Orphanet J Rare Dis 2008
100
16

The Database of Genomic Variants: a curated collection of structural variation in the human genome.
Jeffrey R MacDonald, Robert Ziman, Ryan K C Yuen, Lars Feuk, Stephen W Scherer. Nucleic Acids Res 2014
637
16

Genome-wide copy number variation study in anorectal malformations.
Emily H M Wong, Long Cui, Chun-Laam Ng, Clara S M Tang, Xue-Lai Liu, Man-Ting So, Benjamin Hon-Kei Yip, Guo Cheng, Ruizhong Zhang, Wai-Kiu Tang,[...]. Hum Mol Genet 2013
16
16

Integrated detection and population-genetic analysis of SNPs and copy number variation.
Steven A McCarroll, Finny G Kuruvilla, Joshua M Korn, Simon Cawley, James Nemesh, Alec Wysoker, Michael H Shapero, Paul I W de Bakker, Julian B Maller, Andrew Kirby,[...]. Nat Genet 2008
687
16

Structural variation in the human genome.
Lars Feuk, Andrew R Carson, Stephen W Scherer. Nat Rev Genet 2006
16

Copy number variations in the GATA4, NKX2-5, TBX5, BMP4 CRELD1, and 22q11.2 gene regions in Chinese children with sporadic congenital heart disease.
Zhetao Li, Jiwei Huang, Biao Liang, Dingyuan Zeng, Shiqiang Luo, Tizhen Yan, Fengwen Liao, Jun Huang, Jingwen Li, Ren Cai,[...]. J Clin Lab Anal 2019
8
16

Congenital hyperinsulinism: current status and future perspectives.
Tohru Yorifuji. Ann Pediatr Endocrinol Metab 2014
47
16

The Diagnosis and Management of Hyperinsulinaemic Hypoglycaemia.
Klára Roženková, Maria Güemes, Pratik Shah, Khalid Hussain. J Clin Res Pediatr Endocrinol 2015
33
16

Both Low Blood Glucose and Insufficient Treatment Confer Risk of Neurodevelopmental Impairment in Congenital Hyperinsulinism: A Multinational Cohort Study.
Annett Helleskov, Maria Melikyan, Evgenia Globa, Inna Shcherderkina, Fani Poertner, Anna-Maria Larsen, Karen Filipsen, Klaus Brusgaard, Charlotte Dahl Christiansen, Lars Kjaersgaard Hansen,[...]. Front Endocrinol (Lausanne) 2017
24
16


Genetics of Monogenic Diabetes: Present Clinical Challenges.
Shivani Misra, Katharine R Owen. Curr Diab Rep 2018
26
16

Molecular mechanisms of congenital hyperinsulinism.
Sofia A Rahman, Azizun Nessa, Khalid Hussain. J Mol Endocrinol 2015
39
16

The difficult management of persistent, non-focal congenital hyperinsulinism: A retrospective review from a single, tertiary center.
Amalie G Rasmussen, Maria Melikian, Evgenia Globa, Sönke Detlefsen, Lars Rasmussen, Henrik Petersen, Klaus Brusgaard, Annett H Rasmussen, Michael B Mortensen, Henrik T Christesen. Pediatr Diabetes 2020
4
25

Hyperinsulinaemic hypoglycaemia and diabetes mellitus due to dominant ABCC8/KCNJ11 mutations.
R R Kapoor, S E Flanagan, C T James, J McKiernan, A M Thomas, S C Harmer, J P Shield, A Tinker, S Ellard, K Hussain. Diabetologia 2011
38
16

Clinical and histological heterogeneity of congenital hyperinsulinism due to paternally inherited heterozygous ABCC8/KCNJ11 mutations.
Ved Bhushan Arya, Maria Guemes, Azizun Nessa, Syeda Alam, Pratik Shah, Clare Gilbert, Senthil Senniappan, Sarah E Flanagan, Sian Ellard, Khalid Hussain. Eur J Endocrinol 2014
22
16


Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
16

Clinical and genetic characterization of congenital hyperinsulinism in Spain.
R Martínez, C Fernández-Ramos, A Vela, T Velayos, A Aguayo, I Urrutia, I Rica, L Castaño. Eur J Endocrinol 2016
12
16

Genetic characteristics of patients with congenital hyperinsulinism.
Mary Ellen Vajravelu, Diva D De León. Curr Opin Pediatr 2018
17
16

ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism.
C Bellanné-Chantelot, C Saint-Martin, M-J Ribeiro, C Vaury, V Verkarre, J-B Arnoux, V Valayannopoulos, S Gobrecht, C Sempoux, J Rahier,[...]. J Med Genet 2010
74
16


Genetics of congenital hyperinsulinemic hypoglycemia.
Sarah E Flanagan, Ritika R Kapoor, Khalid Hussain. Semin Pediatr Surg 2011
44
16

Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism.
Ritika R Kapoor, Sarah E Flanagan, Ved Bhushan Arya, Julian P Shield, Sian Ellard, Khalid Hussain. Eur J Endocrinol 2013
122
16

Hyperinsulinaemic hypoglycaemia:genetic mechanisms, diagnosis and management.
Zainaba Mohamed, Ved Bhushan Arya, Khalid Hussain. J Clin Res Pediatr Endocrinol 2012
51
16

Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesia.
Marcus P Kennedy, Heymut Omran, Margaret W Leigh, Sharon Dell, Lucy Morgan, Paul L Molina, Blair V Robinson, Susan L Minnix, Heike Olbrich, Thomas Severin,[...]. Circulation 2007
245
16


The syndrome of left isomerism: sonographic findings and outcome in prenatally diagnosed cases.
Christoph Berg, Annegret Geipel, Daniel Kamil, Mareike Knüppel, Johannes Breuer, Martin Krapp, Ahmet Baschat, Ute Germer, Manfred Hansmann, Ulrich Gembruch. J Ultrasound Med 2005
33
16

High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy.
Nader Nakhleh, Richard Francis, Rachel A Giese, Xin Tian, You Li, Maimoona A Zariwala, Hisato Yagi, Omar Khalifa, Safina Kureshi, Bishwanath Chatterjee,[...]. Circulation 2012
104
16

Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome.
Margaret W Leigh, Jessica E Pittman, Johnny L Carson, Thomas W Ferkol, Sharon D Dell, Stephanie D Davis, Michael R Knowles, Maimoona A Zariwala. Genet Med 2009
234
16

De novo trisomy 20p characterized by array comparative genomic hybridization: report of a novel case and review of the literature.
Luca Bartolini, Stefano Sartori, Elisabetta Lenzini, Chiara Rigon, Elisa Cainelli, Cristina Agrati, Irene Toldo, Marta Donà, Eva Trevisson. Gene 2013
11
16

Establishing norms for intestinal length in children.
Marie-Chantal Struijs, Ivan R Diamond, Nicole de Silva, Paul W Wales. J Pediatr Surg 2009
150
16

Congenital Short Bowel Syndrome: from clinical and genetic diagnosis to the molecular mechanisms involved in intestinal elongation.
Christine S van der Werf, Danny Halim, Joke B G M Verheij, Maria M Alves, Robert M W Hofstra. Biochim Biophys Acta 2015
21
16

Formation of new chromatin domains determines pathogenicity of genomic duplications.
Martin Franke, Daniel M Ibrahim, Guillaume Andrey, Wibke Schwarzer, Verena Heinrich, Robert Schöpflin, Katerina Kraft, Rieke Kempfer, Ivana Jerković, Wing-Lee Chan,[...]. Nature 2016
291
16

Spinal disorders associated with skeletal dysplasias and syndromes.
Debbie Song, Cormac O Maher. Neurosurg Clin N Am 2007
15
16

Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11.
Kamini Kalidas, Adam C Shaw, Andrew H Crosby, Ruth Newbury-Ecob, Lynn Greenhalgh, Isabel K Temple, Caroline Law, Amisha Patel, Michael A Patton, Steve Jeffery. J Hum Genet 2005
19
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.