A citation-based method for searching scientific literature

Katherine Adlington, James Smith, Jason Crabtree, Soe Win, Jade Rennie, Kuresh Khodatars, Elisabeth Rosser, Ian Hall. Am J Med Genet B Neuropsychiatr Genet 2019
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Ethical issues in susceptibility genetic testing for late-onset neurodegenerative diseases.
Amaranta Manrique de Lara, Liliana Soto-Gómez, Elisa Núñez-Acosta, Garbiñe Saruwatari-Zavala, Miguel E Rentería. Am J Med Genet B Neuropsychiatr Genet 2019
1
100

Psychiatric genetics researchers' views on offering return of results to individual participants.
Kristin M Kostick, Cody Brannan, Stacey Pereira, Gabriel Lázaro-Muñoz. Am J Med Genet B Neuropsychiatr Genet 2019
12
33

Attitudes toward the right to autonomous decision-making in psychiatric genetic testing: Controversial and context-dependent.
Jana Strohmaier, Stephanie H Witt, Josef Frank, Noemi Lemme, Laura Flatau, Fabian Streit, Jerome C Foo, Markus Reitt, Dan Rujescu, Thomas G Schulze,[...]. Am J Med Genet B Neuropsychiatr Genet 2019
3
33

Ethical implications of using biobanks and population databases for genetic suicide research.
Jess Shade, Hilary Coon, Anna R Docherty. Am J Med Genet B Neuropsychiatr Genet 2019
3
33


A look into the future? Patients' and health care staff's perception and evaluation of genetic information and the right not to know.
Christian Lenk, Gunnar Duttge, Laura Flatau, Debora Frommeld, Wolfgang Poser, Markus Reitt, Thomas Schulze, Alexandra Weber, Barbara Zoll. Am J Med Genet B Neuropsychiatr Genet 2019
2
50

Psychiatric genetic counseling: A mapping exercise.
Ramona Moldovan, Kevin A McGhee, Domenico Coviello, Anniken Hamang, Angela Inglis, Charlotta Ingvoldstad Malmgren, Maria Johansson-Soller, Mercy Laurino, Bettina Meiser, Lauren Murphy,[...]. Am J Med Genet B Neuropsychiatr Genet 2019
3
33

International Society of Psychiatric Genetics Ethics Committee: Issues facing us.
Gabriel Lázaro-Muñoz, Maya Sabatello, Laura Huckins, Holly Peay, Franziska Degenhardt, Bettina Meiser, Todd Lencz, Takahiro Soda, Anna Docherty, David Crepaz-Keay,[...]. Am J Med Genet B Neuropsychiatr Genet 2019
7
33

Sensitive Periods for the Effect of Childhood Adversity on DNA Methylation: Results From a Prospective, Longitudinal Study.
Erin C Dunn, Thomas W Soare, Yiwen Zhu, Andrew J Simpkin, Matthew J Suderman, Torsten Klengel, Andrew D A C Smith, Kerry J Ressler, Caroline L Relton. Biol Psychiatry 2019
57
33


Child maltreatment, adaptive functioning, and polygenic risk: A structural equation mixture model.
Eric L Thibodeau, Katherine E Masyn, Fred A Rogosch, Dante Cicchetti. Dev Psychopathol 2019
2
50

Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disorders.
Kate Wolfe, André Strydom, Deborah Morrogh, Jennifer Carter, Peter Cutajar, Mo Eyeoyibo, Angela Hassiotis, Jane McCarthy, Raja Mukherjee, Dimitrios Paschos,[...]. Eur J Hum Genet 2016
20
33

Alterations of lateral temporal cortical gray matter and facial memory as vulnerability indicators for schizophrenia: An MRI study in youth at familial high-risk for schizophrenia.
Benjamin K Brent, Isabelle M Rosso, Heidi W Thermenos, Daphne J Holt, Stephen V Faraone, Nikos Makris, Ming T Tsuang, Larry J Seidman. Schizophr Res 2016
6
33

Reversal of proliferation deficits caused by chromosome 16p13.11 microduplication through targeting NFκB signaling: an integrated study of patient-derived neuronal precursor cells, cerebral organoids and in vivo brain imaging.
Mandy Johnstone, Navneet A Vasistha, Miruna C Barbu, Owen Dando, Karen Burr, Edward Christopher, Sophie Glen, Christelle Robert, Rana Fetit, Kenneth G Macleod,[...]. Mol Psychiatry 2019
19
33

Childhood developmental abnormalities in schizophrenia: evidence from high-risk studies.
Laura T Niemi, Jaana M Suvisaari, Annamari Tuulio-Henriksson, Jouko K Lönnqvist. Schizophr Res 2003
192
33

Brain structure in people at ultra-high risk of psychosis, patients with first-episode schizophrenia, and healthy controls: a VBM study.
Igor Nenadic, Maren Dietzek, Nils Schönfeld, Carsten Lorenz, Alexander Gussew, Jürgen R Reichenbach, Heinrich Sauer, Christian Gaser, Stefan Smesny. Schizophr Res 2015
43
33



Familial t(1;11) translocation is associated with disruption of white matter structural integrity and oligodendrocyte-myelin dysfunction.
Navneet A Vasistha, Mandy Johnstone, Samantha K Barton, Steffen E Mayerl, Bhuvaneish Thangaraj Selvaraj, Pippa A Thomson, Owen Dando, Ellen Grünewald, Clara Alloza, Mark E Bastin,[...]. Mol Psychiatry 2019
9
33


Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions.
David M Howard, Mark J Adams, Toni-Kim Clarke, Jonathan D Hafferty, Jude Gibson, Masoud Shirali, Jonathan R I Coleman, Saskia P Hagenaars, Joey Ward, Eleanor M Wigmore,[...]. Nat Neurosci 2019
361
33

A prospective cohort study of childhood behavioral deviance and language abnormalities as predictors of adult schizophrenia.
C E Bearden, I M Rosso, J M Hollister, L E Sanchez, T Hadley, T D Cannon. Schizophr Bull 2000
85
33

Abnormal neuronal differentiation and mitochondrial dysfunction in hair follicle-derived induced pluripotent stem cells of schizophrenia patients.
O Robicsek, R Karry, I Petit, N Salman-Kesner, F-J Müller, E Klein, D Aberdam, D Ben-Shachar. Mol Psychiatry 2013
137
33

The fall of the schizophrenogenic mother.
Anne Harrington. Lancet 2012
13
33


Epigenetic programming by maternal behavior.
Ian C G Weaver, Nadia Cervoni, Frances A Champagne, Ana C D'Alessio, Shakti Sharma, Jonathan R Seckl, Sergiy Dymov, Moshe Szyf, Michael J Meaney. Nat Neurosci 2004
33

No Support for Historical Candidate Gene or Candidate Gene-by-Interaction Hypotheses for Major Depression Across Multiple Large Samples.
Richard Border, Emma C Johnson, Luke M Evans, Andrew Smolen, Noah Berley, Patrick F Sullivan, Matthew C Keller. Am J Psychiatry 2019
155
33

Broad epigenetic signature of maternal care in the brain of adult rats.
Patrick O McGowan, Matthew Suderman, Aya Sasaki, Tony C T Huang, Michael Hallett, Michael J Meaney, Moshe Szyf. PLoS One 2011
264
33


Are there progressive brain changes in schizophrenia? A meta-analysis of structural magnetic resonance imaging studies.
Bayanne Olabi, Ian Ellison-Wright, Andrew M McIntosh, Stephen J Wood, Ed Bullmore, Stephen M Lawrie. Biol Psychiatry 2011
294
33

Behavioral and intellectual markers for schizophrenia in apparently healthy male adolescents.
M Davidson, A Reichenberg, J Rabinowitz, M Weiser, Z Kaplan, M Mark. Am J Psychiatry 1999
411
33

Treatable inborn errors of metabolism presenting as cerebral palsy mimics: systematic literature review.
Emma L Leach, Michael Shevell, Kristin Bowden, Sylvia Stockler-Ipsiroglu, Clara D M van Karnebeek. Orphanet J Rare Dis 2014
34
33

Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
Sheng Chih Jin, Sara A Lewis, Somayeh Bakhtiari, Xue Zeng, Michael C Sierant, Sheetal Shetty, Sandra M Nordlie, Aureliane Elie, Mark A Corbett, Bethany Y Norton,[...]. Nat Genet 2020
20
33

Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy.
Andrés Moreno-De-Luca, Francisca Millan, Denis R Pesacreta, Houda Z Elloumi, Matthew T Oetjens, Claire Teigen, Karen E Wain, Julie Scuffins, Scott M Myers, Rebecca I Torene,[...]. JAMA 2021
8
33

Genomic analysis identifies masqueraders of full-term cerebral palsy.
Yusuke Takezawa, Atsuo Kikuchi, Kazuhiro Haginoya, Tetsuya Niihori, Yurika Numata-Uematsu, Takehiko Inui, Saeko Yamamura-Suzuki, Takuya Miyabayashi, Mai Anzai, Sato Suzuki-Muromoto,[...]. Ann Clin Transl Neurol 2018
31
33


A comparison of genomic diagnostics in adults and children with epilepsy and comorbid intellectual disability.
Katherine A Benson, Maire White, Nicholas M Allen, Susan Byrne, Robert Carton, Elizabeth Comerford, Daniel Costello, Colin Doherty, Brendan Dunleavey, Hany El-Naggar,[...]. Eur J Hum Genet 2020
8
33

Neurodevelopmental Disorders: From Genetics to Functional Pathways.
Ilaria Parenti, Luis G Rabaneda, Hanna Schoen, Gaia Novarino. Trends Neurosci 2020
28
33

Cerebral palsy and genomics: an international consortium.
Alastair H MacLennan, Michael C Kruer, Gareth Baynam, Andres Moreno-De-Luca, Yana A Wilson, Changlian Zhu, Richard F Wintle, Jozef Gecz. Dev Med Child Neurol 2018
9
33

Atypical cerebral palsy: genomics analysis enables precision medicine.
Allison M Matthews, Ingrid Blydt-Hansen, Basmah Al-Jabri, John Andersen, Maja Tarailo-Graovac, Magda Price, Katherine Selby, Michelle Demos, Mary Connolly, Britt Drögemoller,[...]. Genet Med 2019
16
33

Proposed definition and classification of cerebral palsy, April 2005.
Martin Bax, Murray Goldstein, Peter Rosenbaum, Alan Leviton, Nigel Paneth, Bernard Dan, Bo Jacobsson, Diane Damiano. Dev Med Child Neurol 2005
33

Hidden etiology of cerebral palsy: genetic and clinical heterogeneity and efficient diagnosis by next-generation sequencing.
Monica Rosello, Alfonso Caro-Llopis, Carmen Orellana, Silvestre Oltra, Marta Alemany-Albert, Ana V Marco-Hernandez, Sandra Monfort, Laia Pedrola, Francisco Martinez, Miguel Tomás. Pediatr Res 2020
1
100

Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy.
G McMichael, M N Bainbridge, E Haan, M Corbett, A Gardner, S Thompson, B W M van Bon, C L van Eyk, J Broadbent, C Reynolds,[...]. Mol Psychiatry 2015
88
33

Cerebral palsy: clinical care and neurological rehabilitation.
Mindy Lipson Aisen, Danielle Kerkovich, Joelle Mast, Sara Mulroy, Tishya A L Wren, Robert M Kay, Susan A Rethlefsen. Lancet Neurol 2011
162
33

Primary care of adults with developmental disabilities: Canadian consensus guidelines.
William F Sullivan, Joseph M Berg, Elspeth Bradley, Tom Cheetham, Richard Denton, John Heng, Brian Hennen, David Joyce, Maureen Kelly, Marika Korossy,[...]. Can Fam Physician 2011
86
33

Identification and evaluation of mental retardation.
D K Daily, H H Ardinger, G E Holmes. Am Fam Physician 2000
65
33


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.