Table 2 Highly cited papers additional to those highly accessed

[12]

Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication

Blake C Ballif, Aaron Theisen, Justine Coppinger, Gordon C Gowans, Joseph H Hersh, Suneeta Madan-Khetarpal, Karen R Schmidt, Raymond Tervo, Luis F Escobar, Christopher A Friedrich, Marie McDonald, Lindsey Campbell, Jeffrey E Ming, Elaine H Zackai, Bassem A Bejjani, Lisa G Shaffer

Molecular Cytogenetics 2008, 1:8

117

[13]

Chromosomal mosaicism goes global

Ivan Y Iourov, Svetlana G Vorsanova, Yuri B Yurov

Molecular Cytogenetics 2008, 1:26

74

[14]

Microdeletion of 6q16. 1 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case report

Traylor RN, Fan Z, Hudson B, Rosenfeld JA, Shaffer LG, Torchia BS, Ballif BC

Molecular Cytogenetics 2009, 2:17

41

[15]

Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGH

Neill NJ, Torchia BS, Bejjani BA, Shaffer LG, Ballif BC

Molecular Cytogenetics 2010, 3:11

40

[16]

Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype

Sismani C, Kitsiou-Tzeli S, Ioannides M, Christodoulou C, Anastasiadou V, Stylianidou G, Papadopoulou E, Kanavakis E, Kosmaidou-Aravidou Z, Patsalis PC

Molecular Cytogenetics 2008, 1:15

39

[17]

Chromosome distribution in human sperm - a 3D multicolor banding-study

Manvelyan M, Hunstig F, Bhatt S, Mrasek K, Pellestor F, Weise A, Simonyan I, Aroutiounian R, Liehr T

Molecular Cytogenetics 2008, 1:25

34

[18]

GIN'n'CIN hypothesis of brain aging: deciphering the role of somatic genetic instabilities and neural aneuploidy during ontogeny

Yurov YB, Vorsanova SG, Iourov IY

Molecular Cytogenetics 2009, 2:23

29