Julie Steffann

2.7k total citations
67 papers, 1.4k citations indexed

About

Julie Steffann is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Julie Steffann has authored 67 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 28 papers in Genetics and 25 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Julie Steffann's work include Prenatal Screening and Diagnostics (23 papers), Mitochondrial Function and Pathology (17 papers) and Metabolism and Genetic Disorders (12 papers). Julie Steffann is often cited by papers focused on Prenatal Screening and Diagnostics (23 papers), Mitochondrial Function and Pathology (17 papers) and Metabolism and Genetic Disorders (12 papers). Julie Steffann collaborates with scholars based in France, United States and Italy. Julie Steffann's co-authors include Arnold Münnich, Jean‐Paul Bonnefont, Nelly Frydman, Nadine Gigarel, Violaine Kerbrat, Sophie Monnot, René Frydman, Agnès Rötig, Alexandra Benachi and Laëtitia Hesters and has published in prestigious journals such as New England Journal of Medicine, Nature Genetics and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Julie Steffann

62 papers receiving 1.4k citations

Peers

Julie Steffann

GENET

PPCH

SURGE

Juan Chemke Israel

Anas M. Alazami Saudi Arabia

Petra Zwijnenburg Netherlands

Khushnooda Ramzan Saudi Arabia

Ghada M. H. Abdel‐Salam Egypt

Loydie A. Jerome‐Majewska Canada

Virpi Töhönen Sweden

R. Sid Wilroy United States

I. Christopher Lloyd United Kingdom

Ana Elisa C. Billerbeck Brazil

Juan Chemke Israel

Julie Steffann

365 ×0.5

327 ×0.7

GENET

220 ×0.6

PPCH

66 ×0.2

152 ×0.6

SURGE

Citations per year, relative to Julie Steffann Julie Steffann (= 1×) peers Juan Chemke

Countries citing papers authored by Julie Steffann

Since Specialization

Citations

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

Fields of papers citing papers by Julie Steffann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Julie Steffann. 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 Julie Steffann. The network helps show where Julie Steffann may publish in the future.

Co-authorship network of co-authors of Julie Steffann

This figure shows the co-authorship network connecting the top 25 collaborators of Julie Steffann. A scholar is included among the top collaborators of Julie Steffann 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 Julie Steffann. Julie Steffann 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

Sonigo, Charlotte, Noémie Ranisavljevic, T. Anahory, et al.. (2024). Ovarian response in preimplantation genetic testing for myotonic dystrophy type 1. Journal of Assisted Reproduction and Genetics. 42(1). 185–192.

Hesters, Laëtitia, Charlotte Sonigo, Sophie Monnot, et al.. (2023). PGT and deferred embryo transfer: Is blastocyst biopsy more effective than cleaved embryo biopsy?. Journal of Gynecology Obstetrics and Human Reproduction. 53(2). 102718–102718. 1 indexed citations

Sonigo, Charlotte, Laëtitia Hesters, Julie Steffann, et al.. (2022). Second biopsy for embryos with inconclusive results after preimplantation genetic testing: Impact on pregnancy outcomes. Journal of Gynecology Obstetrics and Human Reproduction. 51(8). 102436–102436. 4 indexed citations

Charbit‐Henrion, Fabienne, et al.. (2022). Tubulin mutations in human neurodevelopmental disorders. Seminars in Cell and Developmental Biology. 137. 87–95. 23 indexed citations

Mayeur, Anne, et al.. (2020). CTG Expansion in the DMPK Gene: Semen Quality Assessment and Outcome of Preimplantation Genetic Diagnosis. The Journal of Clinical Endocrinology & Metabolism. 105(4). 1137–1144. 8 indexed citations

Fusco, Francesca, Alessandra Pescatore, Julie Steffann, et al.. (2019). Clinical utility gene card: for incontinentia pigmenti. European Journal of Human Genetics. 27(12). 1894–1900. 14 indexed citations

Bal, Élodie, Emmanuel Laplantine, Yamina Hamel, et al.. (2017). Lack of interaction between NEMO and SHARPIN impairs linear ubiquitination and NF-κB activation and leads to incontinentia pigmenti. Journal of Allergy and Clinical Immunology. 140(6). 1671–1682.e2. 13 indexed citations

Steffann, Julie, et al.. (2013). Parental mosaicism is a pitfall in preimplantation genetic diagnosis of dominant disorders. European Journal of Human Genetics. 22(5). 711–712. 5 indexed citations

Assouline, Zahra, Marguerite Jambou, Marlène Rio, et al.. (2012). A constant and similar assembly defect of mitochondrial respiratory chain complex I allows rapid identification of NDUFS4 mutations in patients with Leigh syndrome. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822(6). 1062–1069. 44 indexed citations

10.

Frydman, René, Nelly Frydman, Julie Steffann, et al.. (2011). Diagnostic pré-implantatoire : dix ans d’expérience en région parisienne : impasse actuelle et solutions à venir. Bulletin de l Académie Nationale de Médecine. 195(4-5). 1005–1014. 2 indexed citations

11.

Steffann, Julie, Nelly Frydman, Philippe Burlet, et al.. (2011). Le diagnostic pré-implantatoire couplé au typage HLA : l’expérience française. Bulletin de l Académie Nationale de Médecine. 195(4-5). 1015–1022. 1 indexed citations

12.

Leshinsky‐Silver, Esther, Anne-Sophie Lèbre, Limor Minai, et al.. (2009). NDUFS4 mutations cause Leigh syndrome with predominant brainstem involvement. Molecular Genetics and Metabolism. 97(3). 185–189. 46 indexed citations

13.

Frydman, René, Laëtitia Hesters, Rénato Fanchin, et al.. (2009). Preimplantation genetic diagnosis: State of the art. European Journal of Obstetrics & Gynecology and Reproductive Biology. 145(1). 9–13. 71 indexed citations

14.

Monnot, Sophie, Bernadette Chadefaux-Vekemans, Joëlle Aupetit, et al.. (2009). Structural insights on pathogenic effects of novel mutations causing pyruvate carboxylase deficiency. Human Mutation. 30(5). 734–740. 25 indexed citations

15.

Gigarel, Nadine, Nelly Frydman, P Burlet, et al.. (2008). Preimplantation genetic diagnosis for autosomal recessive polycystic kidney disease. Reproductive BioMedicine Online. 16(1). 152–158. 30 indexed citations

16.

Burlet, P, Nelly Frydman, Nadine Gigarel, et al.. (2006). Multiple displacement amplification improves PGD for fragile X syndrome. Molecular Human Reproduction. 12(10). 647–652. 53 indexed citations

17.

Feyereisen, E., Violaine Kerbrat, Julie Steffann, et al.. (2005). Myotonic dystrophy: does it affect ovarian follicular status and responsiveness to controlled ovarian stimulation?. Human Reproduction. 21(1). 175–182. 30 indexed citations

18.

Steffann, Julie, Nelly Frydman, P Burlet, et al.. (2005). Le diagnostic préimplantatoire couplé au typage HLA : l'expérience parisienne. Gynécologie Obstétrique & Fertilité. 33(10). 824–827. 3 indexed citations

19.

Gigarel, Nadine, Laure Thuillier, Isabelle Sermet‐Gaudelus, et al.. (2004). Novel CFTR mutations in black cystic fibrosis patients. Clinical Genetics. 65(4). 284–287. 14 indexed citations

20.

Amiel, Jeanne, Yolanda Espinosa‐Parrilla, Julie Steffann, et al.. (2001). Large-Scale Deletions and SMADIP1 Truncating Mutations in Syndromic Hirschsprung Disease with Involvement of Midline Structures. The American Journal of Human Genetics. 69(6). 1370–1377. 79 indexed citations

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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