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Krepischi, Ana CV
129  Ergebnisse:
Personensuche X
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1

Functional assessment of donated human embryos for the gene..:

Ceschin, Ianaê I ; Ceschin, Alvaro P ; Joya, Maria S...
Reproductive BioMedicine Online.  46 (2023)  3 - p. 491-501 , 2023
Link: https://doi.org/10.1016/..
 
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2

KIF11 microdeletion is associated with microcephaly, chorio..:

Malvezzi, João VM ; H Magalhaes, Ingrid ; S Costa, Silvia...
Human Genome Variation.  5 (2018)  1 - p. , 2018
Link: https://doi.org/10.1038/..
 
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3

Pathogenic copy number variants in patients with congenital..:

Correa, Fernanda A. ; Jorge, Alexander AL ; Nakaguma, Marilena...
Clinical Endocrinology.  88 (2018)  3 - p. 425-431 , 2018
Link: https://doi.org/10.1111/..
 
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4

Co-expression network of neural-differentiation genes shows..:

Maschietto, Mariana ; Tahira, Ana C ; Puga, Renato...
BMC Medical Genomics.  8 (2015)  1 - p. , 2015
Link: https://doi.org/10.1186/..
 
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5

The profile and contribution of rare germline copy number v..:

Silva, Amanda G ; Krepischi, Ana CV ; Pearson, Peter L...
Orphanet Journal of Rare Diseases.  9 (2014)  1 - p. 63 , 2014
Link: https://doi.org/10.1186/..
 
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6

Mutational spectrum of WTX, WT1, CTNNB1, APC and PLCG2 gene..:

Barros, Bruna D ; Torrezan, Giovana T ; Ferreira, Elisa N...
BMC Proceedings.  6 (2012)  S6 - p. , 2012
Link: https://doi.org/10.1186/..
 
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7

Germline DNA copy number variation in familial and early-on..:

Krepischi, Ana CV ; Achatz, Maria Isabel W ; Santos, Erika MM...
Breast Cancer Research.  14 (2012)  1 - p. , 2012
Link: https://doi.org/10.1186/..
 
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8

Number of rare germline CNVs and TP53 mutation types:

Silva, Amanda G ; Achatz, Maria Isabel Waddington ; Krepischi, Ana CV..
Orphanet Journal of Rare Diseases.  7 (2012)  1 - p. , 2012
Link: https://doi.org/10.1186/..
 
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9

Breakpoint characterization of a novel large intragenic del..:

Torrezan, Giovana T ; da Silva, Felipe CC ; Krepischi, Ana CV...
BMC Medical Genetics.  12 (2011)  1 - p. , 2011
Link: https://doi.org/10.1186/..
 
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10

Methylome profiling of healthy and central precocious puber..:

Bessa, Danielle, S ; Maschietto, Mariana ; Aylwin, Carlos, Francisco...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13148-018-0581-1.  , 2018
Link: https://hal.sorbonne-uni..
 
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11

KIF11 microdeletion is associated with microcephaly, chorio..:

Malvezzi, João VM ; H Magalhaes, Ingrid ; S Costa, Silvia...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694292/.  , 2018
Link: http://www.ncbi.nlm.nih...
 
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12

Differential DNA Methylation of MicroRNA Genes in Temporal ..:

Villela, Darine ; Ramalho, Rodrigo F ; Silva, Aderbal RT...
qt0m86n4q9.  , 2016
Link: https://escholarship.org..
 
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13

The profile and contribution of rare germline copy number v..:

Silva, Amanda G ; Krepischi, Ana CV ; Pearson, Peter L...
http://www.ojrd.com/content/9/1/63.  , 2014
Link: http://www.ojrd.com/cont..
 
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14

Does germ-line deletion of the PIP gene constitute a widesp..:

Silva, Amanda G ; Krepischi, Ana CV ; Torrezan, Giovana T...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC.  , 2014
Link: http://www.ncbi.nlm.nih...
 
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15

Number of rare germline CNVs and TP53 mutation types:

Silva Amanda G ; Achatz Isabel Maria W ; Krepischi Ana CV..
http://www.ojrd.com/content/7/1/101.  , 2012
Link: https://doi.org/10.1186/..
 
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