J.L. Serre

689 citations

20 papers · 489 indexed · h-index 10

Impact in

Endocrinology, Diabetes and Metabolism top 10%
- Alkaline Phosphatase Research Studies
Rheumatology top 10%
- Heterotopic Ossification and Related Conditions

Papers in

Pulmonary and Respiratory Medicine 10
- Cystic Fibrosis Research Advances 10
- Neonatal Respiratory Health Research 3
- Tracheal and airway disorders 3
Endocrinology, Diabetes and Metabolism 5
- Alkaline Phosphatase Research Studies 4

Co-authors: Étienne Mornet Brigitte Simon‐Bouy J Boué A Boué A. Taillandier Françoise Müller Fran Thomas C Oudet
Journals: Human Genetics (4 papers)Human Mutation (2 papers)European Journal of Human Genetics (2 papers)Clinical Genetics (2 papers)Advances in experimental medicine and biology (1 paper)
Partner nations: France United States Belgium

In The Last Decade

J.L. Serre

20 papers receiving 481 citations

Peers

Countries citing papers authored by J.L. Serre

Since Specialization

Citations

This map shows the geographic impact of J.L. Serre'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 J.L. Serre with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J.L. Serre more than expected).

Fields of papers citing papers by J.L. Serre

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J.L. Serre. 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 J.L. Serre. The network helps show where J.L. Serre may publish in the future.

Co-authors

The 25 scholars most cited alongside J.L. Serre, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with J.L. Serre Line = papers co-authored together J.L. Serre links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Does anonymous sperm donation increase the risk for unions between relatives and the incidence of autosomal recessive diseases due to consanguinity? Human Reproduction ·J.L. Serre, Anne‐Louise Leutenegger, Alain Bernheim, Marc Fellous, 好隆友村, Jean Pierre Siffroi	2013	4
2	A new mechanism of dominance in hypophosphatasia: the mutated protein can disturb the cell localization of the wild-type protein Human Genetics ·Anne-Sophie Lia-Baldini, Isabelle Brun‐Heath, Claire Carrion, Brigitte Simon‐Bouy, J.L. Serre, Mark E. Nuñes, Étienne Mornet	2008	38
3	Childhood Hypophosphatasia Due to a de Novo Missense Mutation in the Tissue-Nonspecific Alkaline Phosphatase Gene The Journal of Clinical Endocrinology & Metabolism ·A. Taillandier, Satu‐Leena Sallinen, Isabelle Brun‐Heath, Philippe de Mazancourt, J.L. Serre, Étienne Mornet	2005	21
4	Predicting the risk of cystic fibrosis with abnormal ultrasound signs of fetal bowel: Results of a French molecular collaborative study based on 641 prospective cases American Journal of Medical Genetics ·Françoise Müller, Brigitte Simon‐Bouy, Emmanuelle Girodon, Nicole Monnier, Marie‐Claire Malinge, J.L. Serre, (unknown)	2002	31
5	Twelve novel mutations in the tissue-nonspecific alkaline phosphatase gene (ALPL) in patients with various forms of hypophosphatasia Human Mutation ·A. Taillandier, Anne-Sophie Lia-Baldini, Penglei Wan, Blaise Robin, Françoise Müller, Brigitte Simon‐Bouy, J.L. Serre, Anne Béra-Louville, M Bonduelle, М. Г. Гаджиев, Dominique Gaillard, С. В. Салита, Ivan Laptev, De Stefano A, Caroline Bertemes, David Sillence, I. Karen Temple, Géraldine Viot, Étienne Mornet	2001	45
6	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 Human Mutation ·A. Taillandier, Adriana Lucia Moros León, Françoise Müller, Brigitte Simon‐Bouy, J.L. Serre, Lynne M. Bird, Rolf E. Brenner, Odile Boute, 真理子岩崎, Dominique Gaillard, P. Heidemann, B Steinmann, M. Wallot, Étienne Mornet	1999	45
7	Cystic fibrosis screening: a fetus with hyperechogenic bowel may be the index case. Journal of Medical Genetics ·Françoise Müller, Marc Dommergues, Brigitte Simon‐Bouy, Claude Férec, J.F. Oury, M. C. Aubry, R. Bessis, E. Vuillard, Érick Denamur, T. Bienvenu, J.L. Serre	1998	28
8	Transition from Normal toPremutated Alleles inFragile X Syndrome Resultsfrom a Multistep Process European Journal of Human Genetics ·Arthy Sri B, Glenn Johnson, Vesna Vujačić, Mladen Jokić, Р. Бахтавар, A. Taillandier, Fran Thomas, Brigitte Simon‐Bouy, J Boué, J.L. Serre, (unknown), (unknown)	1994	8
9	A polymorphic poly-A sequence in the 5? region of the aldosynthase (CYP11B2) gene may be useful in genetic diagnosis of 11?-hydroxylase genes defects Human Genetics ·F. Clot, Marten Jäger, Brigitte Simon‐Bouy, J.L. Serre, B. Aupetit-Faisant, Étienne Mornet	1994	5
10	General Cystic Fibrosis Mutations Are Usually Missense Mutations Affecting Two Specific Protein Domains and Associated with a Specific RFLP Marker Haplotype European Journal of Human Genetics ·J.L. Serre, T. Xiang, Brigitte Simon‐Bouy, J Boué, A Boué	1993	2
11	Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes. PubMed ·C Oudet, Étienne Mornet, J.L. Serre, Fran Thomas, Katia Imaculada Moreira de Oliveira, Christine Kretz, Vesna Vujačić, Isabel Tejada, J Boué, A Boué	1993	111
12	Nine mutations in the cystic fibrosis (CF) gene account for 80% of the CF chromosomes in French patients Clinical Genetics ·Brigitte Simon‐Bouy, Étienne Mornet, J.L. Serre, A. Taillandier, J Boué, A Boué	1991	7
13	Toward a Geographical History of the Predominant and Secondary Mutations in Europe Advances in experimental medicine and biology ·J.L. Serre	1991	1
14	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 Genomics ·J.L. Serre, A. Taillandier, Étienne Mornet, Brigitte Simon‐Bouy, J Boué, A Boué	1991	6
15	The cystic fibrosis ΔF508 mutation in the French population Human Genetics ·Brigitte Simon‐Bouy, Étienne Mornet, J.L. Serre, Insan Fehmi Tunaii, J Boué, A Boué	1990	6
16	Studies of RFLP closely linked to the cystic fibrosis locus throughout Europe lead to new considerations in populations genetics Human Genetics ·J.L. Serre, Brigitte Simon‐Bouy, Étienne Mornet, Yeon Mee Lee, Angeliki Balassopoulou, M. Schwartz, A. Taillandier, (unknown), A. Bou�	1990	76
17	Genetic heterogeneity between two clinical forms of cystic fibrosis evidenced by familial analysis and linked DNA probes Clinical Genetics ·Étienne Mornet, Brigitte Simon‐Bouy, J.L. Serre, Françoise Müller, A. Taillandier, María Martínez, J Boué, A Boué	1989	9
18	GENETIC DIFFERENCES BETWEEN CYSTIC FIBROSIS WITH AND WITHOUT MECONIUM ILEUS The Lancet ·Étienne Mornet, J.L. Serre, Martin Farrall, J Boué, Brigitte Simon‐Bouy, Xavier Estivill, R. Williamson, A Boué	1988	44
19	Social blending and genetical blending Journal of Human Evolution ·J.L. Serre, Debora C. Mendes	1979	1
20	Analyse génétique d'une population présentant des anomalies de fréquence génique Revue Fran&#xE7 aise de Transfusion et Immuno-h&#xE9 matologie ·Neus Ticó-Falguera, Reygan H. Sangalang, MARIE MILLARD, J.L. Serre, Michael S Pasano, C.P. Brizard	1978	1

About J.L. Serre

J.L. Serre is a scholar working on Pulmonary and Respiratory Medicine, Endocrinology, Diabetes and Metabolism, Genetics, Orthopedics and Sports Medicine and Genetics, having authored 20 papers that have together received 489 indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (10 papers), Alkaline Phosphatase Research Studies (4 papers), Neonatal Respiratory Health Research (3 papers), Tracheal and airway disorders (3 papers), Congenital Ear and Nasal Anomalies (3 papers), Hedgehog Signaling Pathway Studies (2 papers), Heterotopic Ossification and Related Conditions (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (133 citations), Rheumatology (103 citations), Genetics (152 citations), Nutrition and Dietetics (75 citations) and Pulmonary and Respiratory Medicine (152 citations). J.L. Serre has collaborated with scholars based in France, United States and Belgium. Frequent co-authors include Étienne Mornet, Brigitte Simon‐Bouy, J Boué, A Boué, A. Taillandier, Françoise Müller, Fran Thomas, C Oudet, Christine Kretz and Isabel Tejada. Their work appears in journals such as Human Genetics, Human Mutation, European Journal of Human Genetics, Clinical Genetics and Advances in experimental medicine and biology.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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