-
1
-
-
84876293343
-
Genetics and genomics of reproductive disorders
-
Oxford, UK: Wiley-Blackwell Jiang Z, Ott TL 1
-
Genetics and genomics of reproductive disorders. Dovc P, Kunej T, Williams GA, Reproductive Genomics of Domestic Animals Oxford, UK: Wiley-Blackwell, Jiang Z, Ott TL, 1 2010 67 97
-
(2010)
Reproductive Genomics of Domestic Animals
, pp. 67-97
-
-
Dovc, P.1
Kunej, T.2
Williams, G.A.3
-
2
-
-
34247626007
-
Cryptorchidism in common eutherian mammals
-
Cryptorchidism in common eutherian mammals. Amann RP, Veeramachaneni DNR, Reproduction 2007 133 3 541 561
-
(2007)
Reproduction
, vol.133
, Issue.3
, pp. 541-561
-
-
Amann, R.P.1
Veeramachaneni, D.N.R.2
-
3
-
-
49449083090
-
Role of hormones, genes, and environment in human cryptorchidism
-
Role of hormones, genes, and environment in human cryptorchidism. Foresta C, Zuccarello D, Garolla A, Ferlin A, Endocr Rev 2008 29 5 560 580
-
(2008)
Endocr Rev
, vol.29
, Issue.5
, pp. 560-580
-
-
Foresta, C.1
Zuccarello, D.2
Garolla, A.3
Ferlin, A.4
-
4
-
-
44649087102
-
Undescended testis: Current theories of etiology
-
Undescended testis: current theories of etiology. Barthold JS, Curr Opin Urol 2008 18 4 395 400
-
(2008)
Curr Opin Urol
, vol.18
, Issue.4
, pp. 395-400
-
-
Barthold, J.S.1
-
7
-
-
43449127550
-
Altered expression of muscle- and cytoskeleton-related genes in a rat strain with inherited cryptorchidism
-
Altered expression of muscle- and cytoskeleton-related genes in a rat strain with inherited cryptorchidism. Barthold JS, McCahan SM, Singh AV, Knudsen TB, Si X, Campion L, Akins RE, J Androl 2008 29 3 352 366
-
(2008)
J Androl
, vol.29
, Issue.3
, pp. 352-366
-
-
Barthold, J.S.1
McCahan, S.M.2
Singh, A.V.3
Knudsen, T.B.4
Si, X.5
Campion, L.6
Akins, R.E.7
-
8
-
-
70449382559
-
Database of cattle candidate genes and genetic markers for milk production and mastitis
-
Database of cattle candidate genes and genetic markers for milk production and mastitis. Ogorevc J, Kunej T, Razpet A, Dovc P, Anim Genet 2009 40 6 832 851
-
(2009)
Anim Genet
, vol.40
, Issue.6
, pp. 832-851
-
-
Ogorevc, J.1
Kunej, T.2
Razpet, A.3
Dovc, P.4
-
9
-
-
79952590481
-
Comparative genomics approach to identify candidate genetic loci for male fertility
-
Comparative genomics approach to identify candidate genetic loci for male fertility. Ogorevc J, Dovc P, Kunej T, Reprod Domest Anim 2011 46 2 229 239
-
(2011)
Reprod Domest Anim
, vol.46
, Issue.2
, pp. 229-239
-
-
Ogorevc, J.1
Dovc, P.2
Kunej, T.3
-
10
-
-
84873907002
-
Obesity gene atlas in mammals
-
Obesity gene atlas in mammals. Kunej T, Jevsinek Skok D, Zorc M, Ogrinc A, Michal JJ, Kovac M, Jiang Z, J Genomics 2012 1 45 55
-
(2012)
J Genomics
, vol.1
, pp. 45-55
-
-
Kunej, T.1
Jevsinek Skok, D.2
Zorc, M.3
Ogrinc, A.4
Michal, J.J.5
Kovac, M.6
Jiang, Z.7
-
11
-
-
84863987708
-
Computational tools for prioritizing candidate genes: Boosting disease gene discovery
-
Computational tools for prioritizing candidate genes: boosting disease gene discovery. Moreau Y, Tranchevent LC, Nat Rev Genet 2012 13 8 523 536
-
(2012)
Nat Rev Genet
, vol.13
, Issue.8
, pp. 523-536
-
-
Moreau, Y.1
Tranchevent, L.C.2
-
12
-
-
84856386410
-
Catalog of MicroRNA Seed Polymorphisms in Vertebrates
-
Catalog of MicroRNA Seed Polymorphisms in Vertebrates. Zorc M, Jevsinek Skok D, Godnic I, Calin GA, Horvat S, Jiang Z, Dovc P, Kunej T, PLoS One 2012 7 1 30737
-
(2012)
PLoS One
, vol.7
, Issue.1
, pp. 530737
-
-
Zorc, M.1
Jevsinek Skok, D.2
Godnic, I.3
Calin, G.A.4
Horvat, S.5
Jiang, Z.6
Dovc, P.7
Kunej, T.8
-
13
-
-
34547589578
-
DAVID Bioinformatics Resources: Expanded annotation database and novel algorithms to better extract biology from large gene lists
-
Web Server Issue
-
DAVID Bioinformatics Resources: expanded annotation database and novel algorithms to better extract biology from large gene lists. da Huang W, Sherman BT, Tan Q, Kir J, Liu D, Bryant D, Guo Y, Stephens R, Baseler MW, Lane HC, Nucleic Acids Res 2007 35 Web Server issue 169 W175
-
(2007)
Nucleic Acids Res
, vol.35
-
-
Da Huang, W.1
Sherman, B.T.2
Tan, Q.3
Kir, J.4
Liu, D.5
Bryant, D.6
Guo, Y.7
Stephens, R.8
Baseler, M.W.9
Lane, H.C.10
-
14
-
-
54949127160
-
IRefIndex: A consolidated protein interaction database with provenance
-
iRefIndex: a consolidated protein interaction database with provenance. Razick S, Magklaras G, Donaldson IM, BMC Bioinforma 2008 9 405
-
(2008)
BMC Bioinforma
, vol.9
, pp. 405
-
-
Razick, S.1
Magklaras, G.2
Donaldson, I.M.3
-
15
-
-
35348891430
-
Network-based classification of breast cancer metastasis
-
Network-based classification of breast cancer metastasis. Chuang HY, Lee E, Liu YT, Lee D, Ideker T, Mol Syst Biol 2007 3 140
-
(2007)
Mol Syst Biol
, vol.3
, pp. 140
-
-
Chuang, H.Y.1
Lee, E.2
Liu, Y.T.3
Lee, D.4
Ideker, T.5
-
16
-
-
77649299348
-
An Atlas of Combinatorial Transcriptional Regulation in Mouse and Man
-
An Atlas of Combinatorial Transcriptional Regulation in Mouse and Man. Ravasi T, Cannistraci CV, Suzuki H, Katayama S, Bajic VB, Tan K, Akalin A, Schmeier S, Kanamori-Katayama M, Bertin N, Cell 2010 140 5 744 752
-
(2010)
Cell
, vol.140
, Issue.5
, pp. 744-752
-
-
Ravasi, T.1
Cannistraci, C.V.2
Suzuki, H.3
Katayama, S.4
Bajic, V.B.5
Tan, K.6
Akalin, A.7
Schmeier, S.8
Kanamori-Katayama, M.9
Bertin, N.10
-
17
-
-
58149194611
-
ConsensusPathDB - A database for integrating human functional interaction networks
-
Database Issue
-
ConsensusPathDB - a database for integrating human functional interaction networks. Kamburov A, Wierling C, Lehrach H, Herwig R, Nucleic Acids Res 2009 37 Database issue 623 D628
-
(2009)
Nucleic Acids Res
, vol.37
-
-
Kamburov, A.1
Wierling, C.2
Lehrach, H.3
Herwig, R.4
-
18
-
-
79953322205
-
PiNGO: A Cytoscape plugin to find candidate genes in biological networks
-
PiNGO: a Cytoscape plugin to find candidate genes in biological networks. Smoot M, Ono K, Ideker T, Maere S, Bioinformatics 2011 27 7 1030 1031
-
(2011)
Bioinformatics
, vol.27
, Issue.7
, pp. 1030-1031
-
-
Smoot, M.1
Ono, K.2
Ideker, T.3
Maere, S.4
-
19
-
-
79551587720
-
Cytoscape 2.8: New features for data integration and network visualization
-
Cytoscape 2.8: new features for data integration and network visualization. Smoot ME, Ono K, Ruscheinski J, Wang PL, Ideker T, Bioinformatics 2011 27 3 431 432
-
(2011)
Bioinformatics
, vol.27
, Issue.3
, pp. 431-432
-
-
Smoot, M.E.1
Ono, K.2
Ruscheinski, J.3
Wang, P.L.4
Ideker, T.5
-
20
-
-
78651324347
-
The STRING database in 2011: Functional interaction networks of proteins, globally integrated and scored
-
Database Issue
-
The STRING database in 2011: functional interaction networks of proteins, globally integrated and scored. Szklarczyk D, Franceschini A, Kuhn M, Simonovic M, Roth A, Minguez P, Doerks T, Stark M, Muller J, Bork P, Nucleic Acids Res 2011 39 Database issue 561 D568
-
(2011)
Nucleic Acids Res
, vol.39
-
-
Szklarczyk, D.1
Franceschini, A.2
Kuhn, M.3
Simonovic, M.4
Roth, A.5
Minguez, P.6
Doerks, T.7
Stark, M.8
Muller, J.9
Bork, P.10
-
21
-
-
75549088251
-
Patrocles: A database of polymorphic miRNA-mediated gene regulation in vertebrates
-
Database Issue
-
Patrocles: a database of polymorphic miRNA-mediated gene regulation in vertebrates. Hiard S, Charlier C, Coppieters W, Georges M, Baurain D, Nucleic Acids Res 2010 38 Database issue 640 D651
-
(2010)
Nucleic Acids Res
, vol.38
-
-
Hiard, S.1
Charlier, C.2
Coppieters, W.3
Georges, M.4
Baurain, D.5
-
22
-
-
0023461382
-
A new type of Robertsonian translocation (1/26) in a bull with unilateral cryptorchidism, probably occurring de novo
-
A new type of Robertsonian translocation (1/26) in a bull with unilateral cryptorchidism, probably occurring de novo. Miyake Y, Kaneda Y, Nihon juigaku zasshi J Vet Sci 1987 49 6 1015 1019
-
(1987)
Nihon Juigaku Zasshi J Vet Sci
, vol.49
, Issue.6
, pp. 1015-1019
-
-
Miyake, Y.1
Kaneda, Y.2
-
23
-
-
0029982691
-
Chromosomal anomalies in cryptorchidism
-
Chromosomal anomalies in cryptorchidism. Sasagawa I, Nakada T, Ishigooka M, Sawamura T, Adachi Y, Hashimoto T, Int Urol Nephrol 1996 28 1 99 102
-
(1996)
Int Urol Nephrol
, vol.28
, Issue.1
, pp. 99-102
-
-
Sasagawa, I.1
Nakada, T.2
Ishigooka, M.3
Sawamura, T.4
Adachi, Y.5
Hashimoto, T.6
-
24
-
-
0030957133
-
Impaired male sex development in an infant with molecularly defined partial 9p monosomy: Implication for a testis forming gene(s) on 9p
-
Impaired male sex development in an infant with molecularly defined partial 9p monosomy: implication for a testis forming gene(s) on 9p. Ogata T, Muroya K, Matsuo N, Hata J, Fukushima Y, Suzuki Y, J Med Genet 1997 34 4 331 334
-
(1997)
J Med Genet
, vol.34
, Issue.4
, pp. 331-334
-
-
Ogata, T.1
Muroya, K.2
Matsuo, N.3
Hata, J.4
Fukushima, Y.5
Suzuki, Y.6
-
25
-
-
0032449507
-
Bilateral cryptorchidism associated with terminal deletion of 10q
-
Bilateral cryptorchidism associated with terminal deletion of 10q. Suzuki Y, Sasagawa I, Nakada T, Onmura Y, Urol Int 1998 61 3 186 187
-
(1998)
Urol Int
, vol.61
, Issue.3
, pp. 186-187
-
-
Suzuki, Y.1
Sasagawa, I.2
Nakada, T.3
Onmura, Y.4
-
26
-
-
43949094375
-
Cryptorchidism associated with 78, XY/79, XXY mosaicism in dog
-
Cryptorchidism associated with 78, XY/79, XXY mosaicism in dog. Goldschmidt B, El-Jaick KB, Souza LM, Carvalho ECQ, Moura VLS, Benevides Filho IM, Israel J Vet Med 2001 56 56 58
-
(2001)
Israel J Vet Med
, vol.56
, pp. 56-58
-
-
Goldschmidt, B.1
El-Jaick, K.B.2
Souza, L.M.3
Carvalho, E.C.Q.4
Moura, V.L.S.5
Benevides Filho, I.M.6
-
27
-
-
0036837465
-
Chromosomal anomalies in cryptorchidism and hypospadias
-
discussion 2172
-
Chromosomal anomalies in cryptorchidism and hypospadias. Moreno-Garcia M, Miranda EB, J Urol 2002 168 5 2170 2172 discussion 2172
-
(2002)
J Urol
, vol.168
, Issue.5
, pp. 2170-2172
-
-
Moreno-Garcia, M.1
Miranda, E.B.2
-
28
-
-
1642464651
-
Familial (9;11)(p22;p15.5)pat translocation and XX sex reversal in a phenotypic boy with cryptorchidism and delayed development
-
Familial (9;11)(p22;p15.5)pat translocation and XX sex reversal in a phenotypic boy with cryptorchidism and delayed development. Prabhakara K, Angalena R, Ramadevi AR, Genetic counseling (Geneva, Switzerland) 2004 15 1 37 41
-
(2004)
Genetic Counseling (Geneva, Switzerland)
, vol.15
, Issue.1
, pp. 37-41
-
-
Prabhakara, K.1
Angalena, R.2
Ramadevi, A.R.3
-
29
-
-
47049097293
-
Autosomic 27 Trisomy in a Standardbred Colt
-
Autosomic 27 Trisomy in a Standardbred Colt. Brito L, Sertich PL, Durkin K, Chowdhary BP, Turner RM, Greene LM, McDonnell S, J Equine Vet Sci 2008 28 7 431 436
-
(2008)
J Equine Vet Sci
, vol.28
, Issue.7
, pp. 431-436
-
-
Brito, L.1
Sertich, P.L.2
Durkin, K.3
Chowdhary, B.P.4
Turner, R.M.5
Greene, L.M.6
McDonnell, S.7
-
30
-
-
44849133641
-
A new look at XXYY syndrome: Medical and psychological features
-
A new look at XXYY syndrome: medical and psychological features. Tartaglia N, Davis S, Hench A, Nimishakavi S, Beauregard R, Reynolds A, Fenton L, Albrecht L, Ross J, Visootsak J, Am J Med Genet A 2008 146A 12 1509 1522
-
(2008)
Am J Med Genet A
, vol.146
, Issue.12
, pp. 1509-1522
-
-
Tartaglia, N.1
Davis, S.2
Hench, A.3
Nimishakavi, S.4
Beauregard, R.5
Reynolds, A.6
Fenton, L.7
Albrecht, L.8
Ross, J.9
Visootsak, J.10
-
31
-
-
77954344374
-
Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with multiple congenital anomalies
-
Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with multiple congenital anomalies. van der Veken LT, Dieleman MM, Douben H, van de Brug JC, van de Graaf R, Hoogeboom AJ, Poddighe PJ, de Klein A, Mol Cytogenet 2010 3 13
-
(2010)
Mol Cytogenet
, vol.3
, pp. 13
-
-
Van Der Veken, L.T.1
Dieleman, M.M.2
Douben, H.3
Van De Brug, J.C.4
Van De Graaf, R.5
Hoogeboom, A.J.6
Poddighe, P.J.7
De Klein, A.8
-
32
-
-
35948956334
-
Genotype/phenotype correlations in two patients with 12q subtelomere deletions
-
Genotype/phenotype correlations in two patients with 12q subtelomere deletions. Niyazov DM, Nawaz Z, Justice AN, Toriello HV, Martin CL, Adam MP, Am J Med Genet A 2007 143A 22 2700 2705
-
(2007)
Am J Med Genet A
, vol.143
, Issue.22
, pp. 2700-2705
-
-
Niyazov, D.M.1
Nawaz, Z.2
Justice, A.N.3
Toriello, H.V.4
Martin, C.L.5
Adam, M.P.6
-
33
-
-
84859005503
-
Clinical description of a patient carrying the smallest reported deletion involving 10p14 region
-
Clinical description of a patient carrying the smallest reported deletion involving 10p14 region. Melis D, Genesio R, Boemio P, Del Giudice E, Cappuccio G, Mormile A, Ronga V, Conti A, Imperati F, Nitsch L, Am J Med Genet A 2012 158A 4 832 835
-
(2012)
Am J Med Genet A
, vol.158
, Issue.4
, pp. 832-835
-
-
Melis, D.1
Genesio, R.2
Boemio, P.3
Del Giudice, E.4
Cappuccio, G.5
Mormile, A.6
Ronga, V.7
Conti, A.8
Imperati, F.9
Nitsch, L.10
-
34
-
-
78149429222
-
Identification of de novo copy number variants associated with human disorders of sexual development
-
Identification of de novo copy number variants associated with human disorders of sexual development. Tannour-Louet M, Han S, Corbett ST, Louet JF, Yatsenko S, Meyers L, Shaw CA, Kang SH, Cheung SW, Lamb DJ, PLoS One 2010 5 10 15392
-
(2010)
PLoS One
, vol.5
, Issue.10
, pp. 515392
-
-
Tannour-Louet, M.1
Han, S.2
Corbett, S.T.3
Louet, J.F.4
Yatsenko, S.5
Meyers, L.6
Shaw, C.A.7
Kang, S.H.8
Cheung, S.W.9
Lamb, D.J.10
-
36
-
-
12444305983
-
Chromosomal region 11p15 is associated with male factor subfertility
-
Chromosomal region 11p15 is associated with male factor subfertility. Gianotten J, van der Veen F, Alders M, Leschot NJ, Tanck MW, Land JA, Kremer JA, Hoefsloot LH, Mannens MM, Lombardi MP, Mol Hum Reprod 2003 9 10 587 592
-
(2003)
Mol Hum Reprod
, vol.9
, Issue.10
, pp. 587-592
-
-
Gianotten, J.1
Van Der Veen, F.2
Alders, M.3
Leschot, N.J.4
Tanck, M.W.5
Land, J.A.6
Kremer, J.A.7
Hoefsloot, L.H.8
Mannens, M.M.9
Lombardi, M.P.10
-
37
-
-
2342517388
-
Molecular and genetic regulation of testis descent and external genitalia development
-
Molecular and genetic regulation of testis descent and external genitalia development. Klonisch T, Fowler PA, Hombach-Klonisch S, Dev Biol 2004 270 1 1 18
-
(2004)
Dev Biol
, vol.270
, Issue.1
, pp. 1-18
-
-
Klonisch, T.1
Fowler, P.A.2
Hombach-Klonisch, S.3
-
38
-
-
0027182741
-
Wt-1 is required for early kidney development
-
WT-1 IS REQUIRED FOR EARLY KIDNEY DEVELOPMENT. Kreidberg JA, Sariola H, Loring JM, Maeda M, Pelletier J, Housman D, Jaenisch R, Cell 1993 74 4 679 691
-
(1993)
Cell
, vol.74
, Issue.4
, pp. 679-691
-
-
Kreidberg, J.A.1
Sariola, H.2
Loring, J.M.3
Maeda, M.4
Pelletier, J.5
Housman, D.6
Jaenisch, R.7
-
39
-
-
0023757134
-
Suprainguinal ectopic scrota of TS inbred rats
-
Suprainguinal ectopic scrota of TS inbred rats. Ikadai H, Ajisawa C, Taya K, Imamichi T, J Reprod Fertil 1988 84 2 701 707
-
(1988)
J Reprod Fertil
, vol.84
, Issue.2
, pp. 701-707
-
-
Ikadai, H.1
Ajisawa, C.2
Taya, K.3
Imamichi, T.4
-
40
-
-
17744375346
-
Altered structure and function of reproductive organs in transgenic male mice overexpressing human aromatase
-
Altered structure and function of reproductive organs in transgenic male mice overexpressing human aromatase. Li X, Nokkala E, Yan W, Streng T, Saarinen N, Warri A, Huhtaniemi I, Santti R, Makela S, Poutanen M, Endocrinology 2001 142 6 2435 2442
-
(2001)
Endocrinology
, vol.142
, Issue.6
, pp. 2435-2442
-
-
Li, X.1
Nokkala, E.2
Yan, W.3
Streng, T.4
Saarinen, N.5
Warri, A.6
Huhtaniemi, I.7
Santti, R.8
Makela, S.9
Poutanen, M.10
-
41
-
-
0033304557
-
Combined hypothalamic-pituitary-gonadal defect in a hypogonadic man with a novel mutation in the DAX-1 gene
-
Combined hypothalamic-pituitary-gonadal defect in a hypogonadic man with a novel mutation in the DAX-1 gene. Caron P, Imbeaud S, Bennet A, Plantavid M, Camerino G, Rochiccioli P, J Clin Endocrinol Metab 1999 84 10 3563 3569
-
(1999)
J Clin Endocrinol Metab
, vol.84
, Issue.10
, pp. 3563-3569
-
-
Caron, P.1
Imbeaud, S.2
Bennet, A.3
Plantavid, M.4
Camerino, G.5
Rochiccioli, P.6
-
42
-
-
0030001706
-
Morphometric study of the gubernaculum in male estrogen receptor mutant mice
-
Morphometric study of the gubernaculum in male estrogen receptor mutant mice. Donaldson KM, Tong SY, Washburn T, Lubahn DB, Eddy EM, Hutson JM, Korach KS, J Androl 1996 17 2 91 95
-
(1996)
J Androl
, vol.17
, Issue.2
, pp. 91-95
-
-
Donaldson, K.M.1
Tong, S.Y.2
Washburn, T.3
Lubahn, D.B.4
Eddy, E.M.5
Hutson, J.M.6
Korach, K.S.7
-
43
-
-
0037106428
-
Mutations of the GREAT gene cause cryptorchidism
-
Mutations of the GREAT gene cause cryptorchidism. Gorlov IP, Kamat A, Bogatcheva NV, Jones E, Lamb DJ, Truong A, Bishop CE, McElreavey K, Agoulnik AI, Hum Mol Genet 2002 11 19 2309 2318
-
(2002)
Hum Mol Genet
, vol.11
, Issue.19
, pp. 2309-2318
-
-
Gorlov, I.P.1
Kamat, A.2
Bogatcheva, N.V.3
Jones, E.4
Lamb, D.J.5
Truong, A.6
Bishop, C.E.7
McElreavey, K.8
Agoulnik, A.I.9
-
44
-
-
0037225692
-
A novel mutation of the insulin-like 3 gene in patients with cryptorchidism
-
A novel mutation of the insulin-like 3 gene in patients with cryptorchidism. Canto P, Escudero I, Soderlund D, Nishimura E, Carranza-Lira S, Gutierrez J, Nava A, Mendez JP, J Hum Genet 2003 48 2 86 90
-
(2003)
J Hum Genet
, vol.48
, Issue.2
, pp. 86-90
-
-
Canto, P.1
Escudero, I.2
Soderlund, D.3
Nishimura, E.4
Carranza-Lira, S.5
Gutierrez, J.6
Nava, A.7
Mendez, J.P.8
-
45
-
-
15944427078
-
Androgen receptor gene CAG and GGC repeat lengths in cryptorchidism
-
Androgen receptor gene CAG and GGC repeat lengths in cryptorchidism. Ferlin A, Garolla A, Bettella A, Bartoloni L, Vinanzi C, Roverato A, Foresta C, Eur J Endocrinol 2005 152 3 419 425
-
(2005)
Eur J Endocrinol
, vol.152
, Issue.3
, pp. 419-425
-
-
Ferlin, A.1
Garolla, A.2
Bettella, A.3
Bartoloni, L.4
Vinanzi, C.5
Roverato, A.6
Foresta, C.7
-
46
-
-
23844471536
-
Association of cryptorchidism with a specific haplotype of the estrogen receptor alpha gene: Implication for the susceptibility to estrogenic environmental endocrine disruptors
-
Association of cryptorchidism with a specific haplotype of the estrogen receptor alpha gene: implication for the susceptibility to estrogenic environmental endocrine disruptors. Yoshida R, Fukami M, Sasagawa I, Hasegawa T, Kamatani N, Ogata T, J Clin Endocrinol Metab 2005 90 8 4716 4721
-
(2005)
J Clin Endocrinol Metab
, vol.90
, Issue.8
, pp. 4716-4721
-
-
Yoshida, R.1
Fukami, M.2
Sasagawa, I.3
Hasegawa, T.4
Kamatani, N.5
Ogata, T.6
-
47
-
-
33745622394
-
Insulin-like factor 3 gene mutations in testicular dysgenesis syndrome: Clinical and functional characterization
-
Insulin-like factor 3 gene mutations in testicular dysgenesis syndrome: clinical and functional characterization. Ferlin A, Bogatcheva NV, Gianesello L, Pepe A, Vinanzi C, Agoulnik AI, Foresta C, Mol Hum Reprod 2006 12 6 401 406
-
(2006)
Mol Hum Reprod
, vol.12
, Issue.6
, pp. 401-406
-
-
Ferlin, A.1
Bogatcheva, N.V.2
Gianesello, L.3
Pepe, A.4
Vinanzi, C.5
Agoulnik, A.I.6
Foresta, C.7
-
48
-
-
33745960757
-
The CAG repeat within the androgen receptor gene and its relationship to cryptorchidism
-
discussion 335
-
The CAG repeat within the androgen receptor gene and its relationship to cryptorchidism. Silva-Ramos M, Oliveira JM, Cabeda JM, Reis A, Soares J, Pimenta A, Int Braz J Urol 2006 32 3 330 334 discussion 335
-
(2006)
Int Braz J Urol
, vol.32
, Issue.3
, pp. 330-334
-
-
Silva-Ramos, M.1
Oliveira, J.M.2
Cabeda, J.M.3
Reis, A.4
Soares, J.5
Pimenta, A.6
-
49
-
-
32944463462
-
Association of cryptorchidism with Gly146Ala polymorphism in the gene for steroidogenic factor-1
-
Association of cryptorchidism with Gly146Ala polymorphism in the gene for steroidogenic factor-1. Wada Y, Okada M, Fukami M, Sasagawa I, Ogata T, Fertil Steril 2006 85 3 787 790
-
(2006)
Fertil Steril
, vol.85
, Issue.3
, pp. 787-790
-
-
Wada, Y.1
Okada, M.2
Fukami, M.3
Sasagawa, I.4
Ogata, T.5
-
50
-
-
33846018526
-
T222P mutation of the insulin-like 3 hormone receptor LGR8 is associated with testicular maldescent and hinders receptor expression on the cell surface membrane
-
T222P mutation of the insulin-like 3 hormone receptor LGR8 is associated with testicular maldescent and hinders receptor expression on the cell surface membrane. Bogatcheva NV, Ferlin A, Feng S, Truong A, Gianesello L, Foresta C, Agoulnik AI, Am J Physiol Endocrinol Metab 2007 292 1 138 E144
-
(2007)
Am J Physiol Endocrinol Metab
, vol.292
, Issue.1
-
-
Bogatcheva, N.V.1
Ferlin, A.2
Feng, S.3
Truong, A.4
Gianesello, L.5
Foresta, C.6
Agoulnik, A.I.7
-
51
-
-
34147200905
-
Novel mutations involving the INSL3 gene associated with cryptorchidism
-
Novel mutations involving the INSL3 gene associated with cryptorchidism. El Houate B, Rouba H, Sibai H, Barakat A, Chafik A, Chadli el B, Imken L, Bogatcheva NV, Feng S, Agoulnik AI, J Urol 2007 177 5 1947 1951
-
(2007)
J Urol
, vol.177
, Issue.5
, pp. 1947-1951
-
-
El Houate, B.1
Rouba, H.2
Sibai, H.3
Barakat, A.4
Chafik, A.5
Chadli El, B.6
Imken, L.7
Bogatcheva, N.V.8
Feng, S.9
Agoulnik, A.I.10
-
52
-
-
33847415031
-
Mutation and polymorphism analyses of INSL3 and LGR8/GREAT in 62 Japanese patients with cryptorchidism
-
Mutation and polymorphism analyses of INSL3 and LGR8/GREAT in 62 Japanese patients with cryptorchidism. Yamazawa K, Wada Y, Sasagawa I, Aoki K, Ueoka K, Ogata T, Horm Res 2007 67 2 73 76
-
(2007)
Horm Res
, vol.67
, Issue.2
, pp. 73-76
-
-
Yamazawa, K.1
Wada, Y.2
Sasagawa, I.3
Aoki, K.4
Ueoka, K.5
Ogata, T.6
-
53
-
-
46449087358
-
Analysis of five single nucleotide polymorphisms in the ESR1 gene in cryptorchidism
-
Analysis of five single nucleotide polymorphisms in the ESR1 gene in cryptorchidism. Wang Y, Barthold J, Figueroa E, Gonzalez R, Noh PH, Wang M, Manson J, Birth Defects Res A Clin Mol Teratol 2008 82 6 482 485
-
(2008)
Birth Defects Res A Clin Mol Teratol
, vol.82
, Issue.6
, pp. 482-485
-
-
Wang, Y.1
Barthold, J.2
Figueroa, E.3
Gonzalez, R.4
Noh, P.H.5
Wang, M.6
Manson, J.7
-
54
-
-
78249260914
-
A missense mutation in LRR8 of RXFP2 is associated with cryptorchidism
-
A missense mutation in LRR8 of RXFP2 is associated with cryptorchidism. Harris RM, Finlayson C, Weiss J, Fisher L, Hurley L, Barrett T, Emge D, Bathgate RA, Agoulnik AI, Jameson JL, Mamm Genome 2010 21 9-10 442 449
-
(2010)
Mamm Genome
, vol.21
, Issue.9-10
, pp. 442-449
-
-
Harris, R.M.1
Finlayson, C.2
Weiss, J.3
Fisher, L.4
Hurley, L.5
Barrett, T.6
Emge, D.7
Bathgate, R.A.8
Agoulnik, A.I.9
Jameson, J.L.10
-
55
-
-
80055058428
-
Molecular analysis of SNP12 in estrogen receptor alpha gene in hypospadiac or cryptorchid patients from Northwestern China
-
Molecular analysis of SNP12 in estrogen receptor alpha gene in hypospadiac or cryptorchid patients from Northwestern China. Tang KF, Zheng JZ, Xing JP, Urol Int 2011 87 3 359 362
-
(2011)
Urol Int
, vol.87
, Issue.3
, pp. 359-362
-
-
Tang, K.F.1
Zheng, J.Z.2
Xing, J.P.3
-
56
-
-
64549132964
-
INSL3/RXFP2 signaling in testicular descent
-
INSL3/RXFP2 signaling in testicular descent. Feng S, Ferlin A, Truong A, Bathgate R, Wade JD, Corbett S, Han S, Tannour-Louet M, Lamb DJ, Foresta C, Ann N Y Acad Sci 2009 1160 197 204
-
(2009)
Ann N y Acad Sci
, vol.1160
, pp. 197-204
-
-
Feng, S.1
Ferlin, A.2
Truong, A.3
Bathgate, R.4
Wade, J.D.5
Corbett, S.6
Han, S.7
Tannour-Louet, M.8
Lamb, D.J.9
Foresta, C.10
-
57
-
-
84856013409
-
A genome-wide association study of men with symptoms of testicular dysgenesis syndrome and its network biology interpretation
-
A genome-wide association study of men with symptoms of testicular dysgenesis syndrome and its network biology interpretation. Dalgaard MD, Weinhold N, Edsgard D, Silver JD, Pers TH, Nielsen JE, Jorgensen N, Juul A, Gerds TA, Giwercman A, J Med Genet 2012 49 1 58 65
-
(2012)
J Med Genet
, vol.49
, Issue.1
, pp. 58-65
-
-
Dalgaard, M.D.1
Weinhold, N.2
Edsgard, D.3
Silver, J.D.4
Pers, T.H.5
Nielsen, J.E.6
Jorgensen, N.7
Juul, A.8
Gerds, T.A.9
Giwercman, A.10
-
58
-
-
0032828249
-
Analysis of homeobox gene HOXA10 mutations in cryptorchidism
-
Analysis of homeobox gene HOXA10 mutations in cryptorchidism. Kolon TF, Wiener JS, Lewitton M, Roth DR, Gonzales ET Jr, Lamb DJ, J Urol 1999 161 1 275 280
-
(1999)
J Urol
, vol.161
, Issue.1
, pp. 275-280
-
-
Kolon, T.F.1
Wiener, J.S.2
Lewitton, M.3
Roth, D.R.4
Gonzales Jr., E.T.5
Lamb, D.J.6
-
59
-
-
77954112496
-
A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism
-
A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism. Teles MG, Trarbach EB, Noel SD, Guerra-Junior G, Jorge A, Beneduzzi D, Bianco SD, Mukherjee A, Baptista MT, Costa EM, Eur J Endocrinol 2010 163 1 29 34
-
(2010)
Eur J Endocrinol
, vol.163
, Issue.1
, pp. 29-34
-
-
Teles, M.G.1
Trarbach, E.B.2
Noel, S.D.3
Guerra-Junior, G.4
Jorge, A.5
Beneduzzi, D.6
Bianco, S.D.7
Mukherjee, A.8
Baptista, M.T.9
Costa, E.M.10
-
60
-
-
34047143237
-
Development of a model for mapping cryptorchidism in sheep and initial evidence for association of INSL3 with the defect
-
Development of a model for mapping cryptorchidism in sheep and initial evidence for association of INSL3 with the defect. Williams GA, Ott TL, Michal JJ, Gaskins CT, Wright RW Jr, Daniels TF, Jiang Z, Anim Genet 2007 38 2 189 191
-
(2007)
Anim Genet
, vol.38
, Issue.2
, pp. 189-191
-
-
Williams, G.A.1
Ott, T.L.2
Michal, J.J.3
Gaskins, C.T.4
Wright Jr., R.W.5
Daniels, T.F.6
Jiang, Z.7
-
61
-
-
43449098565
-
Clinical, cytogenetic and molecular evaluation in a dog with bilateral cryptorchidism and hypospadias
-
Clinical, cytogenetic and molecular evaluation in a dog with bilateral cryptorchidism and hypospadias. Cassata R, Iannuzzi A, Parma P, De Lorenzi L, Peretti V, Perucatti A, Iannuzzi L, Di Meo GP, Cytogenet Genome Res 2008 120 1-2 140 143
-
(2008)
Cytogenet Genome Res
, vol.120
, Issue.1-2
, pp. 140-143
-
-
Cassata, R.1
Iannuzzi, A.2
Parma, P.3
De Lorenzi, L.4
Peretti, V.5
Perucatti, A.6
Iannuzzi, L.7
Di Meo, G.P.8
-
62
-
-
77955159962
-
An association study of 20 candidate genes with cryptorchidism in Siberian Husky dogs
-
An association study of 20 candidate genes with cryptorchidism in Siberian Husky dogs. Zhao X, Du ZQ, Rothschild MF, J Anim Breed Genet 2010 127 4 327 331
-
(2010)
J Anim Breed Genet
, vol.127
, Issue.4
, pp. 327-331
-
-
Zhao, X.1
Du, Z.Q.2
Rothschild, M.F.3
-
63
-
-
33846480134
-
Molecular analysis of estrogen receptor alpha gene AGATA haplotype and SNP12 in European populations: Potential protective effect for cryptorchidism and lack of association with male infertility
-
Molecular analysis of estrogen receptor alpha gene AGATA haplotype and SNP12 in European populations: potential protective effect for cryptorchidism and lack of association with male infertility. Galan JJ, Guarducci E, Nuti F, Gonzalez A, Ruiz M, Ruiz A, Krausz C, Hum Reprod 2007 22 2 444 449
-
(2007)
Hum Reprod
, vol.22
, Issue.2
, pp. 444-449
-
-
Galan, J.J.1
Guarducci, E.2
Nuti, F.3
Gonzalez, A.4
Ruiz, M.5
Ruiz, A.6
Krausz, C.7
-
64
-
-
77956551561
-
Analysis of single nucleotide polymorphisms in the 3′ region of the estrogen receptor 1 gene in normal and cryptorchid Miniature Dachshunds and Chihuahuas
-
Analysis of single nucleotide polymorphisms in the 3′ region of the estrogen receptor 1 gene in normal and cryptorchid Miniature Dachshunds and Chihuahuas. Pathirana IN, Tanaka K, Kawate N, Tsuji M, Kida K, Hatoya S, Inaba T, Tamada H, J Reprod Dev 2010 56 4 405 410
-
(2010)
J Reprod Dev
, vol.56
, Issue.4
, pp. 405-410
-
-
Pathirana, I.N.1
Tanaka, K.2
Kawate, N.3
Tsuji, M.4
Kida, K.5
Hatoya, S.6
Inaba, T.7
Tamada, H.8
-
65
-
-
78650414840
-
ESR1 promoter polymorphism is not associated with nonsyndromic cryptorchidism
-
371 e361-362
-
ESR1 promoter polymorphism is not associated with nonsyndromic cryptorchidism. Lo Giacco D, Ars E, Bassas L, Galan JJ, Rajmil O, Ruiz P, Caffaratti J, Guarducci E, Ruiz-Castane E, Krausz C, Fertil Steril 2011 95 1 369 371 371 e361-362
-
(2011)
Fertil Steril
, vol.95
, Issue.1
, pp. 369-371
-
-
Lo Giacco, D.1
Ars, E.2
Bassas, L.3
Galan, J.J.4
Rajmil, O.5
Ruiz, P.6
Caffaratti, J.7
Guarducci, E.8
Ruiz-Castane, E.9
Krausz, C.10
-
66
-
-
0034067764
-
Absence of mutations involving the INSL3 gene in human idiopathic cryptorchidism
-
Absence of mutations involving the INSL3 gene in human idiopathic cryptorchidism. Krausz C, Quintana-Murci L, Fellous M, Siffroi JP, McElreavey K, Mol Hum Reprod 2000 6 4 298 302
-
(2000)
Mol Hum Reprod
, vol.6
, Issue.4
, pp. 298-302
-
-
Krausz, C.1
Quintana-Murci, L.2
Fellous, M.3
Siffroi, J.P.4
McElreavey, K.5
-
67
-
-
0034939542
-
Ala/Thr60 variant of the Leydig insulin-like hormone is not associated with cryptorchidism in the Japanese population
-
Ala/Thr60 variant of the Leydig insulin-like hormone is not associated with cryptorchidism in the Japanese population. Takahashi I, Takahashi T, Komatsu M, Matsuda J, Takada G, Pediatr Int 2001 43 3 256 258
-
(2001)
Pediatr Int
, vol.43
, Issue.3
, pp. 256-258
-
-
Takahashi, I.1
Takahashi, T.2
Komatsu, M.3
Matsuda, J.4
Takada, G.5
-
68
-
-
0036090566
-
The insulin-3 gene: Lack of a genetic basis for human cryptorchidism
-
The insulin-3 gene: lack of a genetic basis for human cryptorchidism. Baker LA, Nef S, Nguyen MT, Stapleton R, Nordenskjold A, Pohl H, Parada LF, J Urol 2002 167 6 2534 2537
-
(2002)
J Urol
, vol.167
, Issue.6
, pp. 2534-2537
-
-
Baker, L.A.1
Nef, S.2
Nguyen, M.T.3
Stapleton, R.4
Nordenskjold, A.5
Pohl, H.6
Parada, L.F.7
-
69
-
-
3142752729
-
Homeobox HOXA10 gene analysis in cryptorchidism
-
Homeobox HOXA10 gene analysis in cryptorchidism. Bertini V, Bertelloni S, Valetto A, Lala R, Foresta C, Simi P, J Pediatr Endocrinol Metab 2004 17 1 41 45
-
(2004)
J Pediatr Endocrinol Metab
, vol.17
, Issue.1
, pp. 41-45
-
-
Bertini, V.1
Bertelloni, S.2
Valetto, A.3
Lala, R.4
Foresta, C.5
Simi, P.6
-
70
-
-
40849119749
-
The leucine-rich repeat-containing G protein-coupled receptor 8 gene T222P mutation does not cause cryptorchidism
-
The leucine-rich repeat-containing G protein-coupled receptor 8 gene T222P mutation does not cause cryptorchidism. Nuti F, Marinari E, Erdei E, El-Hamshari M, Echavarria MG, Ars E, Balercia G, Merksz M, Giachini C, Shaeer KZ, J Clin Endocrinol Metab 2008 93 3 1072 1076
-
(2008)
J Clin Endocrinol Metab
, vol.93
, Issue.3
, pp. 1072-1076
-
-
Nuti, F.1
Marinari, E.2
Erdei, E.3
El-Hamshari, M.4
Echavarria, M.G.5
Ars, E.6
Balercia, G.7
Merksz, M.8
Giachini, C.9
Shaeer, K.Z.10
-
71
-
-
40049094341
-
Polymorphisms of the luteinizing hormone/chorionic gonadotropin receptor gene: Association with maldescended testes and male infertility
-
Polymorphisms of the luteinizing hormone/chorionic gonadotropin receptor gene: association with maldescended testes and male infertility. Simoni M, Tuttelmann F, Michel C, Bockenfeld Y, Nieschlag E, Gromoll J, Pharmacogenet Genomics 2008 18 3 193 200
-
(2008)
Pharmacogenet Genomics
, vol.18
, Issue.3
, pp. 193-200
-
-
Simoni, M.1
Tuttelmann, F.2
Michel, C.3
Bockenfeld, Y.4
Nieschlag, E.5
Gromoll, J.6
-
72
-
-
0038511309
-
Y chromosome microdeletions in infertile men with cryptorchidism
-
Y chromosome microdeletions in infertile men with cryptorchidism. Kunej T, Zorn B, Peterlin B, Fertil Steril 2003 79 Suppl 3 1559 1565
-
(2003)
Fertil Steril
, vol.79
, Issue.SUPPL. 3
, pp. 1559-1565
-
-
Kunej, T.1
Zorn, B.2
Peterlin, B.3
-
73
-
-
33645719977
-
Screening for y microdeletions in men with testicular cancer and undescended testis
-
Screening for Y microdeletions in men with testicular cancer and undescended testis. Bor P, Hindkjaer J, Kolvraa S, Rossen P, von der Maase H, Jorgensen TM, Sorensen VT, Eiberg H, Ingerslev HJ, J Assist Reprod Genet 2006 23 1 41 45
-
(2006)
J Assist Reprod Genet
, vol.23
, Issue.1
, pp. 41-45
-
-
Bor, P.1
Hindkjaer, J.2
Kolvraa, S.3
Rossen, P.4
Von Der Maase, H.5
Jorgensen, T.M.6
Sorensen, V.T.7
Eiberg, H.8
Ingerslev, H.J.9
-
74
-
-
48549102317
-
Do microdeletions in the AZF region of the y chromosome accompany cryptorchidism in Turkish children?
-
Do microdeletions in the AZF region of the Y chromosome accompany cryptorchidism in Turkish children? Gurbuz N, Ozbay B, Aras B, Tasci AI, Int Urol Nephrol 2008 40 3 577 581
-
(2008)
Int Urol Nephrol
, vol.40
, Issue.3
, pp. 577-581
-
-
Gurbuz, N.1
Ozbay, B.2
Aras, B.3
Tasci, A.I.4
-
75
-
-
24344432027
-
Expression of aromatase and oestrogen receptors in reproductive tissues of the stallion and a single cryptorchid visualised by means of immunohistochemistry
-
Expression of aromatase and oestrogen receptors in reproductive tissues of the stallion and a single cryptorchid visualised by means of immunohistochemistry. Hejmej A, Gorazd M, Kosiniak-Kamysz K, Wiszniewska B, Sadowska J, Bilinska B, Domest Anim Endocrinol 2005 29 3 534 547
-
(2005)
Domest Anim Endocrinol
, vol.29
, Issue.3
, pp. 534-547
-
-
Hejmej, A.1
Gorazd, M.2
Kosiniak-Kamysz, K.3
Wiszniewska, B.4
Sadowska, J.5
Bilinska, B.6
-
76
-
-
67649125104
-
Gene expression alterations in cryptorchid males using spermatozoal microarray analysis
-
Gene expression alterations in cryptorchid males using spermatozoal microarray analysis. Nguyen MT, Delaney DP, Kolon TF, Fertil Steril 2009 92 1 182 187
-
(2009)
Fertil Steril
, vol.92
, Issue.1
, pp. 182-187
-
-
Nguyen, M.T.1
Delaney, D.P.2
Kolon, T.F.3
-
77
-
-
0031907740
-
Congenital undescended testes in neonatal pigs and the effect of exogenous calcitonin gene-related peptide
-
Congenital undescended testes in neonatal pigs and the effect of exogenous calcitonin gene-related peptide. Hutson JM, Watts LM, Farmer PJ, J Urol 1998 159 3 1025 1028
-
(1998)
J Urol
, vol.159
, Issue.3
, pp. 1025-1028
-
-
Hutson, J.M.1
Watts, L.M.2
Farmer, P.J.3
-
78
-
-
10244270755
-
Preliminary data suggest that mutations in the CgRP pathway are not involved in human sporadic cryptorchidism
-
Preliminary data suggest that mutations in the CgRP pathway are not involved in human sporadic cryptorchidism. Zuccarello D, Morini E, Douzgou S, Ferlin A, Pizzuti A, Salpietro DC, Foresta C, Dallapiccola B, J Endocrinol Invest 2004 27 8 760 764
-
(2004)
J Endocrinol Invest
, vol.27
, Issue.8
, pp. 760-764
-
-
Zuccarello, D.1
Morini, E.2
Douzgou, S.3
Ferlin, A.4
Pizzuti, A.5
Salpietro, D.C.6
Foresta, C.7
Dallapiccola, B.8
-
79
-
-
22044435794
-
Neurofibromatosis-Noonan syndrome: Molecular evidence of the concurrence of both disorders in a patient
-
Neurofibromatosis-Noonan syndrome: molecular evidence of the concurrence of both disorders in a patient. Bertola DR, Pereira AC, Passetti F, de Oliveira PS, Messiaen L, Gelb BD, Kim CA, Krieger JE, Am J Med Genet A 2005 136 3 242 245
-
(2005)
Am J Med Genet A
, vol.136
, Issue.3
, pp. 242-245
-
-
Bertola, D.R.1
Pereira, A.C.2
Passetti, F.3
De Oliveira, P.S.4
Messiaen, L.5
Gelb, B.D.6
Kim, C.A.7
Krieger, J.E.8
-
80
-
-
80053203956
-
RASopathies: Clinical Diagnosis in the First Year of Life
-
RASopathies: Clinical Diagnosis in the First Year of Life. Digilio MC, Lepri F, Baban A, Dentici ML, Versacci P, Capolino R, Ferese R, De Luca A, Tartaglia M, Marino B, Molecular syndromology 2011 1 6 282 289
-
(2011)
Molecular Syndromology
, vol.1
, Issue.6
, pp. 282-289
-
-
Digilio, M.C.1
Lepri, F.2
Baban, A.3
Dentici, M.L.4
Versacci, P.5
Capolino, R.6
Ferese, R.7
De Luca, A.8
Tartaglia, M.9
Marino, B.10
-
81
-
-
33845900943
-
Germline gain-of-function mutations in SOS1 cause Noonan syndrome
-
Germline gain-of-function mutations in SOS1 cause Noonan syndrome. Roberts AE, Araki T, Swanson KD, Montgomery KT, Schiripo TA, Joshi VA, Li L, Yassin Y, Tamburino AM, Neel BG, Nat Genet 2007 39 1 70 74
-
(2007)
Nat Genet
, vol.39
, Issue.1
, pp. 70-74
-
-
Roberts, A.E.1
Araki, T.2
Swanson, K.D.3
Montgomery, K.T.4
Schiripo, T.A.5
Joshi, V.A.6
Li, L.7
Yassin, Y.8
Tamburino, A.M.9
Neel, B.G.10
-
82
-
-
34547539552
-
Germline gain-of-function mutations in RAF1 cause Noonan syndrome
-
Germline gain-of-function mutations in RAF1 cause Noonan syndrome. Razzaque MA, Nishizawa T, Komoike Y, Yagi H, Furutani M, Amo R, Kamisago M, Momma K, Katayama H, Nakagawa M, Nat Genet 2007 39 8 1013 1017
-
(2007)
Nat Genet
, vol.39
, Issue.8
, pp. 1013-1017
-
-
Razzaque, M.A.1
Nishizawa, T.2
Komoike, Y.3
Yagi, H.4
Furutani, M.5
Amo, R.6
Kamisago, M.7
Momma, K.8
Katayama, H.9
Nakagawa, M.10
-
83
-
-
77956552656
-
Nonlinear dimension reduction and clustering by Minimum Curvilinearity unfold neuropathic pain and tissue embryological classes
-
Nonlinear dimension reduction and clustering by Minimum Curvilinearity unfold neuropathic pain and tissue embryological classes. Cannistraci CV, Ravasi T, Montevecchi FM, Ideker T, Alessio M, Bioinformatics 2010 26 18 531 i539
-
(2010)
Bioinformatics
, vol.26
, Issue.18
-
-
Cannistraci, C.V.1
Ravasi, T.2
Montevecchi, F.M.3
Ideker, T.4
Alessio, M.5
-
84
-
-
77951952127
-
The power of protein interaction networks for associating genes with diseases
-
England
-
The power of protein interaction networks for associating genes with diseases. Navlakha S, Kingsford C, Bioinformatics (Oxford, England) 2010 26 1057 1063 England
-
(2010)
Bioinformatics (Oxford, England)
, vol.26
, pp. 1057-1063
-
-
Navlakha, S.1
Kingsford, C.2
-
85
-
-
34547488336
-
Probing genetic overlap among complex human phenotypes
-
Probing genetic overlap among complex human phenotypes. Rzhetsky A, Wajngurt D, Park N, Zheng T, P Natl Acad Sci USA 2007 104 28 11694 11699
-
(2007)
P Natl Acad Sci USA
, vol.104
, Issue.28
, pp. 11694-11699
-
-
Rzhetsky, A.1
Wajngurt, D.2
Park, N.3
Zheng, T.4
-
86
-
-
43249114206
-
Network-based global inference of human disease genes
-
Network-based global inference of human disease genes. Wu X, Jiang R, Zhang MQ, Li S, Mol Syst Biol 2008 4 189
-
(2008)
Mol Syst Biol
, vol.4
, pp. 189
-
-
Wu, X.1
Jiang, R.2
Zhang, M.Q.3
Li, S.4
-
87
-
-
58049220319
-
Align human interactome with phenome to identify causative genes and networks underlying disease families
-
Align human interactome with phenome to identify causative genes and networks underlying disease families. Wu X, Liu Q, Jiang R, Bioinformatics 2009 25 1 98 104
-
(2009)
Bioinformatics
, vol.25
, Issue.1
, pp. 98-104
-
-
Wu, X.1
Liu, Q.2
Jiang, R.3
-
89
-
-
33845545435
-
The modular nature of genetic diseases
-
The modular nature of genetic diseases. Oti M, Brunner HG, Clin Genet 2007 71 1 1 11
-
(2007)
Clin Genet
, vol.71
, Issue.1
, pp. 1-11
-
-
Oti, M.1
Brunner, H.G.2
-
90
-
-
79955644649
-
Polymorphisms in microRNA targets: A source of new molecular markers for male reproduction
-
Polymorphisms in microRNA targets: a source of new molecular markers for male reproduction. Ogorevc J, Dovc P, Kunej T, Asian J Androl 2011 13 3 505 508
-
(2011)
Asian J Androl
, vol.13
, Issue.3
, pp. 505-508
-
-
Ogorevc, J.1
Dovc, P.2
Kunej, T.3
-
91
-
-
78650557277
-
The glypican 3-hosted murine mir717 gene: Sequence conservation, seed region polymorphisms and putative targets
-
The glypican 3-hosted murine mir717 gene: sequence conservation, seed region polymorphisms and putative targets. Kunej T, Skok DJ, Horvat S, Dovc P, Jiang Z, Int J Biol Sci 2010 6 7 769 772
-
(2010)
Int J Biol Sci
, vol.6
, Issue.7
, pp. 769-772
-
-
Kunej, T.1
Skok, D.J.2
Horvat, S.3
Dovc, P.4
Jiang, Z.5
|