Ludovica Picchetta
Overview
Explore the profile of Ludovica Picchetta including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
8
Citations
12
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Van Der Kelen A, Uyttebroeck S, Van de Voorde S, Picchetta L, Segers I, Vlaeminck J, et al.
J Assist Reprod Genet
. 2025 Jan;
PMID: 39871066
Purpose: Primary ovarian insufficiency (POI) is an important cause of female infertility, stemming from follicle dysfunction or premature oocyte depletion. Pathogenic variants in genes such as NOBOX, GDF9, BMP15, and...
2.
Figliuzzi M, Bori L, Ottolini C, Picchetta L, Caroselli S, Reverenna M, et al.
Fertil Steril
. 2024 Nov;
PMID: 39510239
Objective: To assess whether segmental aneuploid embryos display unique morphokinetic patterns. Design: Retrospective multicenter study including a total of 7,027 embryos cultured between 2016 and 2021 in three European in ...
3.
Iturriaga A, Mounts E, Picchetta L, Vega C, Mulas F, Ottolini C, et al.
Fertil Steril
. 2024 Jul;
122(5):789-798.
PMID: 38996904
Objective: To evaluate the technical accuracy, inheritance, and pathogenicity of small copy number variants (CNVs) detected by a targeted next-generation sequencing-based preimplantation genetic testing for aneuploidy (PGT-A) platform. Design: Retrospective...
4.
Bredbacka P, Capalbo A, Kananen K, Picchetta L, Tomas C
Hum Reprod
. 2023 Aug;
38(9):1700-1704.
PMID: 37528053
During IVF treatments, normal fertilization is generally evidenced by the appearance of two pronuclei, one arising from the oocyte and the other from the male gamete. Embryos derived from zygotes...
5.
Picchetta L, Ottolini C, ONeill H, Capalbo A
F S Sci
. 2023 Mar;
4(2S):17-26.
PMID: 36948460
Segmental aneuploidies (SAs) are structural imbalances, namely, gains or losses, involving a chromosomal segment. Most preimplantation genetic testing platforms can detect segmental imbalances greater than 5-10 Mb, either full or...
6.
Capalbo A, Gabbiato I, Caroselli S, Picchetta L, Cavalli P, Lonardo F, et al.
J Assist Reprod Genet
. 2022 Nov;
39(11):2581-2593.
PMID: 36370240
Purpose: Carrier screening (CS) is a term used to describe a genetic test performed on individuals without family history of genetic disorders, to investigate the carrier status for pathogenic variants...
7.
Update on preimplantation genetic testing for aneuploidy and outcomes of embryos with mosaic results
Dahdouh E, Mourad A, Balayla J, Sylvestre C, Brezina P, Kutteh W, et al.
Minerva Obstet Gynecol
. 2022 Oct;
75(5):468-481.
PMID: 36255164
Preimplantation genetic testing for aneuploidy (PGT-A) is used as a frequent add-on for in-vitro fertilization (IVF) to improve clinical outcomes. The purpose is to select a euploid embryo following chromosomal...
8.
Picchetta L, Caroselli S, Figliuzzi M, Cogo F, Zambon P, Costa M, et al.
J Assist Reprod Genet
. 2022 Feb;
39(4):847-860.
PMID: 35124783
The most important factor associated with oocytes' developmental competence has been widely identified as the presence of chromosomal abnormalities. However, growing application of genome-wide sequencing (GS) in population diagnostics has...
9.
Thuring M, Knuchel R, Picchetta L, Keller D, Schmidli T, Provenzano M
Front Immunol
. 2020 Sep;
11:1244.
PMID: 32922383
Prostate cancer (PCa) is a slow-growing tumor representing one of the major causes of all new cancer cases and cancer mortality in men worldwide. Although screening methods for PCa have...