Jean-Louis Serre
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Explore the profile of Jean-Louis Serre including associated specialties, affiliations and a list of published articles.
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Articles
14
Citations
222
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Recent Articles
1.
Jalkh N, Sahbatou M, Chouery E, Megarbane A, Leutenegger A, Serre J
Eur J Hum Genet
. 2015 Sep;
23(10):1434.
PMID: 26376682
No abstract available.
2.
Jalkh N, Sahbatou M, Chouery E, Megarbane A, Leutenegger A, Serre J
Eur J Hum Genet
. 2014 Nov;
23(10):1364-9.
PMID: 25424710
Consanguineous marriages have been widely practiced in several global communities with varying rates depending on religion, culture, and geography. In consanguineous marriages, parents pass to their children autozygous segments known...
3.
Serre J, Leutenegger A, Bernheim A, Fellous M, Rouen A, Siffroi J
Hum Reprod
. 2013 Dec;
29(3):394-9.
PMID: 24345578
In France gamete donation and notably sperm donation are anonymous. It has been claimed that anonymous artificial insemination by donor (AID) could highly contribute to an increase in the level...
4.
Jeru I, Hayrapetyan H, Duquesnoy P, Cochet E, Serre J, Feingold J, et al.
PLoS One
. 2009 Nov;
4(10):e7676.
PMID: 19888326
Background: Identification of modifier genes and characterization of their effects represent major challenges in human genetics. SAA1 is one of the few modifiers identified in humans: this gene influences the...
5.
Fauvert D, Brun-Heath I, Lia-Baldini A, Bellazi L, Taillandier A, Serre J, et al.
BMC Med Genet
. 2009 Jun;
10:51.
PMID: 19500388
Background: Mild hypophosphatasia (HPP) phenotype may result from ALPL gene mutations exhibiting residual alkaline phosphatase activity or from severe heterozygous mutations exhibiting a dominant negative effect. In order to determine...
6.
Bonaiti-Pellie C, Arveux P, Billette de Villemeur A, Dantchev N, Elbaz A, Fabre-Guillevin E, et al.
Med Sci (Paris)
. 2009 Jan;
25(1):93-7.
PMID: 19154701
No abstract available.
7.
Simon-Bouy B, Taillandier A, Fauvert D, Brun-Heath I, Serre J, Armengod C, et al.
Prenat Diagn
. 2008 Oct;
28(11):993-8.
PMID: 18925618
Objective: We studied hypophosphatasia (HP) mutations in 19 cases prenatally detected by ultrasonography without familial history of HP. We correlated the mutations with the reported ultrasound signs, and discussed genetic...
8.
Chouery E, Delague V, Bergougnoux A, Koussa S, Serre J, Megarbane A
Hum Mutat
. 2008 Jun;
29(9):E194-204.
PMID: 18546367
A genome-wide screen using 382 STR markers to localize and identify the gene implicated in early-onset dementia (EOD) without bone cysts in a Lebanese family with three affected subjects was...
9.
Brun-Heath I, Lia-Baldini A, Maillard S, Taillandier A, Utsch B, Nunes M, et al.
Eur J Med Genet
. 2007 Aug;
50(5):367-78.
PMID: 17719863
Hypophosphatasia is a rare genetic disease characterized by diminished bone and tooth mineralization due to deficient activity of tissue-nonspecific alkaline phosphatase (TNSALP). The disease is clinically heterogeneous due to different...
10.
Jalkh N, Genin E, Chouery E, Delague V, Medlej-Hashim M, Idrac C, et al.
Ann Hum Genet
. 2007 Aug;
72(Pt 1):41-7.
PMID: 17711558
Haplotype analysis of 376 Familial Mediterranean Fever (FMF) patients and 100 controls from Lebanon was performed using 4 microsatellite loci to study founder effects for the five most frequent mutations...