A citation-based method for searching scientific literature

Sriparna Basu, Ashok Kumar, B K Das. Am J Med Genet A 2009
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Prenatal diagnosis of trisomy 13: analysis of 28 cases.
Csaba Papp, Artur Beke, Zoltan Ban, Zsanett Szigeti, Erno Toth-Pal, Zoltan Papp. J Ultrasound Med 2006
26
75

Holoprosencephaly: An update on cytogenetic abnormalities.
Claude Bendavid, Valérie Dupé, Lucie Rochard, Isabelle Gicquel, Christèle Dubourg, Véronique David. Am J Med Genet C Semin Med Genet 2010
36
75

Trisomy 13 syndrome: prenatal US findings in a review of 33 cases.
C D Lehman, D A Nyberg, T C Winter, R P Kapur, R G Resta, D A Luthy. Radiology 1995
93
75

Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly.
Jeffrey E Ming, Michelle E Kaupas, Erich Roessler, Han G Brunner, Mahin Golabi, Mustafa Tekin, Robert F Stratton, Eva Sujansky, Sherri J Bale, Maximilian Muenke. Hum Genet 2002
159
50

Prenatal diagnosis of triploidy associated with holoprosencephaly: a case report and review of the literature.
Gharid N Bekdache, Muzib Begam, Walaa Al Safi, Hisham Mirghani. Am J Perinatol 2009
6
50

Clinical characteristics and survival of trisomy 13 in a medical center in Taiwan, 1985-2004.
Hsiang-Yu Lin, Shuan-Pei Lin, Yen-Jiun Chen, Chyong-Hsin Hsu, Hsin-An Kao, Ming-Ren Chen, Han-Yang Hung, Che-Sheng Ho, Jui-Hsing Chang, Fu-Yuan Huang,[...]. Pediatr Int 2007
32
50

The full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanism.
Erich Roessler, Felicitas Lacbawan, Christèle Dubourg, Aimee Paulussen, Jos Herbergs, Ute Hehr, Claude Bendavid, Nan Zhou, Maia Ouspenskaia, Sherri Bale,[...]. Hum Mutat 2009
49
50


Evaluating the incidence and likelihood ratios for chromosomal abnormalities in fetuses with common central nervous system malformations.
Katherine R Goetzinger, David M Stamilio, Jeffrey M Dicke, George A Macones, Anthony O Odibo. Am J Obstet Gynecol 2008
36
50


An epidemiological study of holoprosencephaly from a regional congenital anomaly register: 1995-2004.
S Ong, A Tonks, E R Woodward, M P Wyldes, M D Kilby. Prenat Diagn 2007
30
50

Holoprosencephaly flashcards: A summary for the clinician.
Benjamin D Solomon, Daniel E Pineda-Alvarez, Sandra Mercier, Manu S Raam, Sylvie Odent, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
16
50

Risk factors for non-syndromic holoprosencephaly in the National Birth Defects Prevention Study.
Eric A Miller, Sonja A Rasmussen, Anna Maria Siega-Riz, Jaime L Frías, Margaret A Honein. Am J Med Genet C Semin Med Genet 2010
43
50

The molecular genetics of holoprosencephaly.
Erich Roessler, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
157
50

Non-genetic risk factors for holoprosencephaly.
Candice Y Johnson, Sonja A Rasmussen. Am J Med Genet C Semin Med Genet 2010
46
50

Amelia, cleft lip, and holoprosencephaly: a distinct entity.
Ariana Kariminejad, Payman Goodarzi, Alaleh Asghari-Roodsari, Mohamad Hasan Kariminejad. Am J Med Genet A 2009
3
66

Holoprosencephaly and craniosynostosis: A report of two siblings and review of the literature.
Manu S Raam, Benjamin D Solomon, Stavit A Shalev, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
11
50

Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly.
Erich Roessler, Wuhong Pei, Maia V Ouspenskaia, Jayaprakash D Karkera, Jorge Ivan Veléz, Sharmilla Banerjee-Basu, Gretchen Gibney, Philip J Lupo, Laura E Mitchell, Jeffrey A Towbin,[...]. Mol Genet Metab 2009
51
50

Abnormal sterol metabolism in holoprosencephaly.
Dorothea Haas, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
22
50

Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.
Erich Roessler, Yang-Zhu Du, Jose L Mullor, Esther Casas, William P Allen, Gabriele Gillessen-Kaesbach, Elizabeth R Roeder, Jeffrey E Ming, Ariel Ruiz i Altaba, Maximilian Muenke. Proc Natl Acad Sci U S A 2003
237
50

Holoprosencephaly, polydactyly and normal chromosomes: pseudo-trisomy 13?
B G Hewitt, M J Seller, C P Bennett, D M Maxwell. Clin Genet 1989
21
50

Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination.
K W Gripp, D Wotton, M C Edwards, E Roessler, L Ades, P Meinecke, A Richieri-Costa, E H Zackai, J Massagué, M Muenke,[...]. Nat Genet 2000
301
50


Recurrent triploidy of maternal origin.
Francesco Brancati, Rita Mingarelli, Bruno Dallapiccola. Eur J Hum Genet 2003
22
25

The pathology of trisomy 13 syndrome. A study of 12 cases.
P Moerman, J P Fryns, K van der Steen, A Kleczkowska, J Lauweryns. Hum Genet 1988
62
25

Functional analysis of mutations in TGIF associated with holoprosencephaly.
Kenia B El-Jaick, Shannon E Powers, Laurent Bartholin, Kenneth R Myers, Jin Hahn, Ieda M Orioli, Maia Ouspenskaia, Felicitas Lacbawan, Erich Roessler, David Wotton,[...]. Mol Genet Metab 2007
55
25




13q Deletion and central nervous system anomalies: further insights from karyotype-phenotype analyses of 14 patients.
Lucia Ballarati, Elena Rossi, Maria Teresa Bonati, Stefania Gimelli, Paola Maraschio, Palma Finelli, Sabrina Giglio, Elisabetta Lapi, Maria Francesca Bedeschi, Silvana Guerneri,[...]. J Med Genet 2007
92
25

Holoprosencephaly.
D M Peebles. Prenat Diagn 1998
36
25

Mosaic trisomy 9 and lobar holoprosencephaly.
Marion Gérard-Blanluet, Claude Danan, Martine Sinico, Françoise Lelong, Elsa Borghi, Gilles Dassieu, Jean-Claude Janaud, Sylvie Odent, Férechté Encha-Razavi. Am J Med Genet 2002
12
25


Mitochondrial NADH-dehydrogenase polymorphisms as sporadic breast cancer risk factor.
Anna M Czarnecka, Aleksandra Klemba, Tomasz Krawczyk, Marek Zdrozny, Rebecca S Arnold, Ewa Bartnik, John A Petros. Oncol Rep 2010
15
25

Elevated B-cell activating factor BAFF, but not APRIL, correlates with CSF cerebellar autoantibodies in pediatric opsoclonus-myoclonus syndrome.
V Fühlhuber, S Bick, A Kirsten, A Hahn, T Gerriets, M Tschernatsch, M Kaps, K T Preissner, F Blaes, S Altenkämper. J Neuroimmunol 2009
29
25

Breast feeding, parental allergy and asthma in children followed for 8 years. The PIAMA birth cohort study.
S Scholtens, A H Wijga, B Brunekreef, M Kerkhof, M O Hoekstra, J Gerritsen, R Aalberse, J C de Jongste, H A Smit. Thorax 2009
64
25

Translation of questions: the International Study of Asthma and Allergies in Childhood (ISAAC) experience.
P Ellwood, H Williams, N Aït-Khaled, B Björkstén, C Robertson. Int J Tuberc Lung Dis 2009
50
25

Introduction to the American Journal of Medical Genetics Part C on holoprosencephaly.
Maximilian Muenke, Benjamin D Solomon, Sylvie Odent. Am J Med Genet C Semin Med Genet 2010
4
25

Rescue of the spinal muscular atrophy phenotype in a mouse model by early postnatal delivery of SMN.
Kevin D Foust, Xueyong Wang, Vicki L McGovern, Lyndsey Braun, Adam K Bevan, Amanda M Haidet, Thanh T Le, Pablo R Morales, Mark M Rich, Arthur H M Burghes,[...]. Nat Biotechnol 2010
507
25

Synergism between pyronaridine and retinol in Plasmodium falciparum in vitro.
Pippa Proell, Kanungnit Congpuong, Franz F Reinthaler, Gunther Wernsdorfer, Ursula Wiedermann, Walther H Wernsdorfer. Wien Klin Wochenschr 2009
4
25

Evaluation of receptor expression on immune system cells in the peripheral blood of asthmatic children undergoing food challenges.
Aneta Krogulska, Krystyna Wasowska-Królikowska, Ewa Polakowska, Slawomir Chrul. Int Arch Allergy Immunol 2009
1
100

Promotion and provision of drinking water in schools for overweight prevention: randomized, controlled cluster trial.
Rebecca Muckelbauer, Lars Libuda, Kerstin Clausen, André Michael Toschke, Thomas Reinehr, Mathilde Kersting. Pediatrics 2009
196
25


Monitoring for multidrug-resistant Plasmodium falciparum isolates and analysis of pyrimethamine resistance evolution in Uige province, Angola.
Michela Menegon, Richard J Pearce, Walter O Inojosa, Vincenzo Pisani, Paulo M Abel, Alexandre Matondo, Zeno Bisoffi, Giancarlo Majori, Rosalynn Ord, David C Warhurst,[...]. Trop Med Int Health 2009
23
25

Pharmacodynamic interaction between mefloquine and retinol in Plasmodium falciparum in vitro.
Maria Gruber, Gunther Wernsdorfer, Wichai Satimai, Ursula Wiedermann, Kanungnit Congpuong, Walther H Wernsdorfer. Wien Klin Wochenschr 2009
8
25

Barkhof magnetic resonance imaging criteria predict early relapse in pediatric multiple sclerosis.
Rinze F Neuteboom, Immy A Ketelslegers, Maartje Boon, Coriene E Catsman-Berrevoets, Rogier Q Hintzen. Pediatr Neurol 2010
10
25

The association between atopy and childhood/adolescent leukemia: a meta-analysis.
Amy M Linabery, Anne M Jurek, Sue Duval, Julie A Ross. Am J Epidemiol 2010
63
25

Pharmacokinetics of artemether-lumefantrine and artesunate-amodiaquine in children in Kampala, Uganda.
Julia Mwesigwa, Sunil Parikh, Bryan McGee, Polina German, Troy Drysdale, Joan N Kalyango, Tamara D Clark, Grant Dorsey, Niklas Lindegardh, Anna Annerberg,[...]. Antimicrob Agents Chemother 2010
59
25


Is multiple sclerosis a mitochondrial disease?
Peizhong Mao, P Hemachandra Reddy. Biochim Biophys Acta 2010
147
25


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.