Literature DB >> 19107955

Genetic tools and algorithms for gene discovery in major congenital anomalies.

Patricia K Donahoe, Kristin M Noonan, Kasper Lage.   

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Year:  2009        PMID： 19107955      PMCID： PMC2880860          DOI： 10.1002/bdra.20546

Source DB:  PubMed          Journal:  Birth Defects Res A Clin Mol Teratol        ISSN： 1542-0752


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  46 in total

Review 1.  Network biology: understanding the cell's functional organization.

Authors:  Albert-László Barabási; Zoltán N Oltvai
Journal:  Nat Rev Genet       Date:  2004-02       Impact factor: 53.242

2.  Molecular characterization of del(8)(p23.1p23.1) in a case of congenital diaphragmatic hernia.

Authors:  Osamu Shimokawa; Noriko Miyake; Takazumi Yoshimura; Nadiya Sosonkina; Naoki Harada; Takeshi Mizuguchi; Shinji Kondoh; Tatsuya Kishino; Tohru Ohta; Visser Remco; Takeshi Takashima; Akira Kinoshita; Koichiro Yoshiura; Norio Niikawa; Naomichi Matsumoto
Journal:  Am J Med Genet A       Date:  2005-07-01       Impact factor: 2.802

3.  The human disease network.

Authors:  Kwang-Il Goh; Michael E Cusick; David Valle; Barton Childs; Marc Vidal; Albert-László Barabási
Journal:  Proc Natl Acad Sci U S A       Date:  2007-05-14       Impact factor: 11.205

Review 4.  Brain evolution and uniqueness in the human genome.

Authors:  Jordan P Amadio; Christopher A Walsh
Journal:  Cell       Date:  2006-09-22       Impact factor: 41.582

Review 5.  Congenital diaphragmatic hernia (CDH) etiology as revealed by pathway genetics.

Authors:  Sibel Kantarci; Patricia K Donahoe
Journal:  Am J Med Genet C Semin Med Genet       Date:  2007-05-15       Impact factor: 3.908

6.  Hospital stays, hospital charges, and in-hospital deaths among infants with selected birth defects--United States, 2003.

Authors: 
Journal:  MMWR Morb Mortal Wkly Rep       Date:  2007-01-19       Impact factor: 17.586

7.  Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization.

Authors:  M Klaassens; M van Dooren; H J Eussen; H Douben; A T den Dekker; C Lee; P K Donahoe; R J Galjaard; N Goemaere; R R de Krijger; C Wouters; J Wauters; B A Oostra; D Tibboel; A de Klein
Journal:  Am J Hum Genet       Date:  2005-03-04       Impact factor: 11.025

8.  Identifying autism loci and genes by tracing recent shared ancestry.

Authors:  Eric M Morrow; Seung-Yun Yoo; Steven W Flavell; Tae-Kyung Kim; Yingxi Lin; Robert Sean Hill; Nahit M Mukaddes; Soher Balkhy; Generoso Gascon; Asif Hashmi; Samira Al-Saad; Janice Ware; Robert M Joseph; Rachel Greenblatt; Danielle Gleason; Julia A Ertelt; Kira A Apse; Adria Bodell; Jennifer N Partlow; Brenda Barry; Hui Yao; Kyriacos Markianos; Russell J Ferland; Michael E Greenberg; Christopher A Walsh
Journal:  Science       Date:  2008-07-11       Impact factor: 47.728

9.  Shared genetic causes of cardiac hypertrophy in children and adults.

Authors:  Hiroyuki Morita; Heidi L Rehm; Andres Menesses; Barbara McDonough; Amy E Roberts; Raju Kucherlapati; Jeffrey A Towbin; J G Seidman; Christine E Seidman
Journal:  N Engl J Med       Date:  2008-04-09       Impact factor: 91.245

10.  Integrative analysis for finding genes and networks involved in diabetes and other complex diseases.

Authors:  Regine Bergholdt; Zenia M Størling; Kasper Lage; E Olof Karlberg; Páll I Olason; Mogens Aalund; Jørn Nerup; Søren Brunak; Christopher T Workman; Flemming Pociot
Journal:  Genome Biol       Date:  2007       Impact factor: 13.583
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  1 in total

1.  Copy number detection in discordant monozygotic twins of Congenital Diaphragmatic Hernia (CDH) and Esophageal Atresia (EA) cohorts.

Authors:  Danielle Veenma; Erwin Brosens; Elisabeth de Jong; Cees van de Ven; Connie Meeussen; Titia Cohen-Overbeek; Marjan Boter; Hubertus Eussen; Hannie Douben; Dick Tibboel; Annelies de Klein
Journal:  Eur J Hum Genet       Date:  2011-11-09       Impact factor: 4.246
  1 in total

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