A. Taillandier

1.6k total citations
27 papers, 993 citations indexed

About

A. Taillandier is a scholar working on Endocrinology, Diabetes and Metabolism, Rheumatology and Nutrition and Dietetics. According to data from OpenAlex, A. Taillandier has authored 27 papers receiving a total of 993 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Endocrinology, Diabetes and Metabolism, 15 papers in Rheumatology and 12 papers in Nutrition and Dietetics. Recurrent topics in A. Taillandier's work include Alkaline Phosphatase Research Studies (17 papers), Heterotopic Ossification and Related Conditions (14 papers) and Selenium in Biological Systems (12 papers). A. Taillandier is often cited by papers focused on Alkaline Phosphatase Research Studies (17 papers), Heterotopic Ossification and Related Conditions (14 papers) and Selenium in Biological Systems (12 papers). A. Taillandier collaborates with scholars based in France, United States and Germany. A. Taillandier's co-authors include Étienne Mornet, Brigitte Simon‐Bouy, Delphine Fauvert, Isabelle Brun‐Heath, Jean‐Louis Serre, Françoise Müller, Anne-Sophie Lia-Baldini, J.L. Serre, Philippe de Mazancourt and Rolf E. Brenner and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Genomics and Human Mutation.

In The Last Decade

A. Taillandier

27 papers receiving 961 citations

Peers

Countries citing papers authored by A. Taillandier

Since Specialization

Citations

This map shows the geographic impact of A. Taillandier's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by A. Taillandier with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A. Taillandier more than expected).

Fields of papers citing papers by A. Taillandier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A. Taillandier. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by A. Taillandier. The network helps show where A. Taillandier may publish in the future.

Co-authorship network of co-authors of A. Taillandier

This figure shows the co-authorship network connecting the top 25 collaborators of A. Taillandier. A scholar is included among the top collaborators of A. Taillandier based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with A. Taillandier. A. Taillandier is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Utility of genetic testing for prenatal presentations of hypophosphatasia 2021 ·Molecular Genetics and Metabolism ·(unknown), A. Taillandier, (unknown), (unknown), Estelle Colin, (unknown), Anya Rothenbühler, Jean‐Pierre Salles, Deborah Wenkert, Andreas Zankl, Christine Muti, Séverine Bacrot, Brigitte Simon‐Bouy, Étienne Mornet	4
2	A Molecular‐Based Estimation of the Prevalence of Hypophosphatasia in the European Population 2011 ·Annals of Human Genetics ·Étienne Mornet, (unknown), A. Taillandier, Delphine Fauvert, Brigitte Simon‐Bouy	164
3	A sequence variation in the promoter of the placental alkaline phosphatase gene (ALPP) is associated with allele-specific expression in human term placenta 2010 ·Placenta ·(unknown), (unknown), (unknown), Isabelle Brun‐Heath, A. Taillandier, Philippe de Mazancourt, Marie‐Noëlle Dieudonné, Étienne Mornet	5
4	Delayed transport of tissue-nonspecific alkaline phosphatase with missense mutations causing hypophosphatasia 2007 ·European Journal of Medical Genetics ·Isabelle Brun‐Heath, Anne-Sophie Lia-Baldini, Stéphane Maillard, A. Taillandier, Boris Utsch, Mark E. Nuñes, Jean‐Louis Serre, Étienne Mornet	29
5	A case of lethal hypophosphatasia providing new insights into the perinatal benign form of hypophosphatasia and expression of the ALPL gene 2007 ·Clinical Genetics ·Isabelle Brun‐Heath, E Chabrol, Mark A. Fox, (unknown), Christine Petit, A. Taillandier, Philippe de Mazancourt, (unknown), Étienne Mornet	12
6	Characterization of Missense Mutations and Large Deletions in the ALPL Gene by Sequencing and Quantitative Multiplex PCR of Short Fragments 2006 ·Genetic Testing ·Marc Spentchian, Isabelle Brun‐Heath, A. Taillandier, Delphine Fauvert, Jean‐Louis Serre, Brigitte Simon‐Bouy, Filipa Carvalho, (unknown), Sarju Mehta, Grit Müller, Saskia A.J. Lesnik Oberstein, Gönül Oğur, Saba Sharif, Étienne Mornet	20
7	Childhood Hypophosphatasia Due to a de Novo Missense Mutation in the Tissue-Nonspecific Alkaline Phosphatase Gene 2005 ·The Journal of Clinical Endocrinology & Metabolism ·A. Taillandier, Satu‐Leena Sallinen, Isabelle Brun‐Heath, Philippe de Mazancourt, J.L. Serre, Étienne Mornet	21
8	Characterization of 11 novel mutations in the tissue non-specific alkaline phosphatase gene responsible for hypophosphatasia and genotype–phenotype correlations 2004 ·Molecular Genetics and Metabolism ·Isabelle Brun‐Heath, A. Taillandier, Jean‐Louis Serre, Étienne Mornet	27
9	Five years of molecular diagnosis of Fragile X syndrome (1997–2001): A collaborative study reporting 95% of the activity in France 2004 ·American Journal of Medical Genetics Part A ·Valérie Biancalana, Chérif Beldjord, A. Taillandier, (unknown), Véronica Cusin, (unknown), Christophe Philippe, Jean‐Louis Mandel, (unknown)	29
10	Evidence of a founder effect for the tissue-nonspecific alkaline phosphatase (TNSALP) gene E174K mutation in hypophosphatasia patients 2002 ·European Journal of Human Genetics ·Muriel Hérasse, Marc Spentchian, A. Taillandier, Étienne Mornet	27
11	A molecular approach to dominance in hypophosphatasia 2001 ·Human Genetics ·Anne-Sophie Lia-Baldini, Françoise Müller, A. Taillandier, (unknown), (unknown), Blaise Robin, Brigitte Simon‐Bouy, (unknown), (unknown), Éric Bieth, (unknown), (unknown), Jingjing Hu, H P Krohn, Mark E. Nuñes, (unknown)	88
12	Parental origin of the extra chromosome in prenatally diagnosed fetal trisomy 21 2000 ·Human Genetics ·Françoise Müller, (unknown), A. Taillandier, J.-F. Oury, Étienne Mornet	34
13	Characterization of eleven novel mutations (M45L, R119H, 544delG, G145V, H154Y, C184Y, D289V, 862+5A, 1172delC, R411X, E459K) in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in patients with severe hypophosphatasia 1999 ·Human Mutation ·A. Taillandier, (unknown), Françoise Müller, Brigitte Simon‐Bouy, J.L. Serre, Lynne M. Bird, Rolf E. Brenner, Odile Boute, (unknown), Dominique Gaillard, P. Heidemann, B Steinmann, M. Wallot, Étienne Mornet	45
14	Identification of fifteen novel mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in European patients with severe hypophosphatasia 1998 ·European Journal of Human Genetics ·Étienne Mornet, A. Taillandier, (unknown), Fiona Kaper, Françoise Müller, Rolf E. Brenner, (unknown), Peter Freisinger, (unknown), M. Le Merrer, J.F. Oury, H Plauchu, Roberta Puddu, (unknown), Andrea Superti‐Furga, (unknown), (unknown), Brigitte Simon‐Bouy	97
15	Recurrent and unexpected segregation of the FMR1 CGG repeat in a family with fragile X syndrome 1996 ·Human Genetics ·Étienne Mornet, (unknown), A. Taillandier, Brigitte Simon‐Bouy, Jean‐Louis Serre	14
16	Transition from Normal toPremutated Alleles inFragile X Syndrome Resultsfrom a Multistep Process 1994 ·European Journal of Human Genetics ·(unknown), (unknown), (unknown), Mladen Jokić, (unknown), A. Taillandier, Fran Thomas, Brigitte Simon‐Bouy, J Boué, J.L. Serre, (unknown), (unknown)	8
17	Nine mutations in the cystic fibrosis (CF) gene account for 80% of the CF chromosomes in French patients 1991 ·Clinical Genetics ·Brigitte Simon‐Bouy, Étienne Mornet, J.L. Serre, A. Taillandier, J Boué, A Boué	7
18	The ΔF508 mutation in mild adult forms of cystic fibrosis (CF) 1991 ·Clinical Genetics ·Brigitte Simon‐Bouy, Étienne Mornet, A. Taillandier, Jean‐Louis Serre, Joëlle Boué, A Boué	3
19	Nearly 80% of cystic fibrosis heterozygotes and 64% of couples at risk may be detected through a unique screening of four mutations by ASO reverse dot blot 1991 ·Genomics ·J.L. Serre, A. Taillandier, Étienne Mornet, Brigitte Simon‐Bouy, J Boué, A Boué	6
20	Studies of RFLP closely linked to the cystic fibrosis locus throughout Europe lead to new considerations in populations genetics 1990 ·Human Genetics ·J.L. Serre, Brigitte Simon‐Bouy, Étienne Mornet, (unknown), Angeliki Balassopoulou, M. Schwartz, A. Taillandier, (unknown), A. Bou�	76

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