Elisabetta Lapi

3.1k citations

48 papers · 957 indexed · h-index 18

Impact in

Developmental Biology top 5%
- Congenital limb and hand anomalies
Developmental Neuroscience top 5%
- Williams Syndrome Research

Papers in ⓘ

Developmental Biology 4
Developmental Neuroscience 7
- Williams Syndrome Research 7

Co-authors: Stefano Stagi (24 shared papers)Maurizio de Martino (17 shared papers)Francesco Chiarelli (13 shared papers)Salvatore Seminara (8 shared papers)Roberto Salti (7 shared papers)Sabrina Giglio (7 shared papers)G. Bindi (6 shared papers)Maria Luisa Giovannucci Uzielli (6 shared papers)
Journals: HORMONES (3 papers)BMC Endocrine Disorders (2 papers)Clinical Endocrinology (2 papers)Human Molecular Genetics (1 paper)European Journal of Human Genetics (1 paper)
Partner nations: Italy Mexico United Kingdom

In The Last Decade

Elisabetta Lapi

48 papers receiving 935 citations

Peers

Countries citing papers authored by Elisabetta Lapi

Since Specialization

Citations

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

Fields of papers citing papers by Elisabetta Lapi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Elisabetta Lapi, 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 Elisabetta Lapi Line = papers co-authored together Elisabetta Lapi links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 48 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract Proceedings of the National Academy of Sciences ·Frances R. Goodman, Stefan Mundlos, Yasuteru Muragaki, Dian Donnai, M. L. Giovannucci-Uzielli, Elisabetta Lapi, F. Majewski, Julie McGaughran, C McKeown, William Reardon, Joseph Upton, R M Winter, Bjørn R. Olsen, Peter Scambler	1997	170
2	The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith–Wiedemann syndrome and Silver–Russell syndrome cases Human Molecular Genetics ·Nicoletta Chiesa, Agostina De Crescenzo, Kankadeb Mishra, Lucia Perone, Massimo Carella, Orazio Palumbo, Alessandro Mussa, Angela Sparago, Flavia Cerrato, Silvia Russo, Elisabetta Lapi, Maria Vittoria Cubellis, Chandrasekhar Kanduri, Margherita Silengo, Andrea Riccio, Giovanni Battista Ferrero	2011	98
3	Mutations in the nebulin gene can cause severe congenital nemaline myopathy Neuromuscular Disorders ·Carina Wallgren‐Pettersson, Kati Donner, Caroline A. Sewry, Emilia Bijlsma, Martin Lammens, Kate Bushby, Maria Luisa Giovannucci Uzielli, Elisabetta Lapi, Sylvie Odent, Zühal Akçören, Haluk Topaloğlu, Katarina Pelin	2002	67
4	Premature ovarian failure (POF) and fragile X premutation females: From POF to fragile X carrier identification, from fragile X carrier diagnosis to POF association data American Journal of Medical Genetics ·Maria Luisa Giovannucci Uzielli, Silvia Guarducci, Elisabetta Lapi, Antonella Cecconi, U. Ricci, G. Ricotti, Claudia Biondi, Benedetta Scarselli, F. Vieri, P. Scarnato, F Gori, A. Sereni	1999	65
5	Identification and characterization of seven novel mutations of elastin gene in a cohort of patients affected by supravalvular aortic stenosis European Journal of Human Genetics ·Lucia Micale, Maria Giuseppina Turturo, Carmela Fusco, Bartolomeo Augello, L.A. Pérez Jurado, Claudia Izzi, M. Cristina Digilio, Donatella Milani, Elisabetta Lapi, Leopoldo Zelante, Giuseppe Merla	2009	44
6	Epigenetic control of the immune system: a lesson from Kabuki syndrome Immunologic Research ·Stefano Stagi, Anna Virginia Gulino, Elisabetta Lapi, Donato Rigante	2015	40
7	Thyroid function and morphology in patients affected by Williams syndrome Clinical Endocrinology ·Stefano Stagi, G. Bindi, Anna Silvia Neri, Elisabetta Lapi, Stefania Losi, R. Jenuso, Roberto Salti, Francesco Chiarelli	2005	37
8	Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome Clinical Genetics ·Ilse Wieland, Carola I. Weidner, Roberto Ciccone, Elisabetta Lapi, Donna M. McDonald‐McGinn, (unknown), Sibylle Jakubiczka, H. Collmann, Orsetta Zuffardi, Elaine H. Zackai, Peter Wieacker	2007	32
9	Determinants of Vitamin D Levels in Children and Adolescents with Down Syndrome International Journal of Endocrinology ·Stefano Stagi, Elisabetta Lapi, Silvia Romano, Sara Bargiacchi, Alice Brambilla, Sabrina Giglio, Salvatore Seminara, Maurizio de Martino	2015	28
10	Bone Mineral Status in Children and Adolescents with Klinefelter Syndrome International Journal of Endocrinology ·Stefano Stagi, Mariarosaria Di Tommaso, Cristina Manoni, Perla Scalini, Francesco Chiarelli, Alberto Verrotti, Elisabetta Lapi, Sabrina Giglio, Laura Dosa, Maurizio de Martino	2016	27
11	Thyroid function and morphology in subjects with microdeletion of chromosome 22q11 (del(22)(q11)) Clinical Endocrinology ·Stefano Stagi, Elisabetta Lapi, Eleonora Gambineri, Roberto Salti, Maurizio Genuardi, Gloria Colarusso, Camilla Conti, R. Jenuso, Francesco Chiarelli, Chiara Azzari, Maurizio de Martino	2009	24
12	Policaptil Gel Retard® significantly reduces body mass index and hyperinsulinism and may decrease the risk of type 2 diabetes mellitus (T2DM) in obese children and adolescents with family history of obesity and T2DM The Italian Journal of Pediatrics/Italian journal of pediatrics ·Stefano Stagi, Elisabetta Lapi, Salvatore Seminara, Paola Pelosi, Paolo Greco, Laura Capirchio, M Strano, Sabrina Giglio, Francesco Chiarelli, Maurizio de Martino	2015	23
13	Partial growth hormone deficiency and changed bone quality and mass in type I trichorhinophalangeal syndrome American Journal of Medical Genetics Part A ·Stefano Stagi, G. Bindi, F. Galluzzi, Elisabetta Lapi, Roberto Salti, Francesco Chiarelli	2008	21
14	Williams-Beuren Syndrome Is a Genetic Disorder Associated with Impaired Glucose Tolerance and Diabetes in Childhood and Adolescence: New Insights from a Longitudinal Study Hormone Research in Paediatrics ·Stefano Stagi, Elisabetta Lapi, Cecilia Cecchi, Francesco Chiarelli, M D'Avanzo, Salvatore Seminara, Maurizio de Martino	2014	19
15	Bone density and metabolism in subjects with microdeletion of chromosome 22q11 (del22q11) European Journal of Endocrinology ·Stefano Stagi, Elisabetta Lapi, Eleonora Gambineri, Cristina Manoni, Maurizio Genuardi, Gloria Colarusso, Camilla Conti, Francesco Chiarelli, Maurizio de Martino, Chiara Azzari	2010	19
16	A SOX3 (Xq26.3-27.3) duplication in a boy with growth hormone deficiency, ocular dyspraxia, and intellectual disability: A long-term follow-up and literature review HORMONES ·Stefano Stagi, Elisabetta Lapi, Maria A. Pantaleo, Giovanna Traficante, Sabrina Giglio, Salvatore Seminara, Maurizio de Martino	2014	19
17	Spectrum and distribution of MECP2 mutations in 64 Italian Rett syndrome girls: tentative genotype/phenotype correlation Brain and Development ·Laura Giunti, Sara Pelagatti, Valentina Lazzerini, Silvia Guarducci, Elisabetta Lapi, Simona Coviello, Antonella Cecconi, L. Ombroni, Elena Andreucci, Ilaria Sani, A Brusaferri, Alberto Lasagni, G. Ricotti, Bruno Giometto, P. Nicolao, Paolo Gasparini, Matteo Granatiero, Maria Luisa Giovannucci Uzielli	2001	18
18	Precocious Puberty in a Girl with Floating-Harbor Syndrome Journal of Pediatric Endocrinology and Metabolism ·Stefano Stagi, Francesco Galluzzi, G. Bindi, Elisabetta Lapi, Costanza Cecchi, Roberto Salti, Francesco Chiarelli	2007	17
19	A new case of de novo 6q24.2-q25.2 deletion on paternal chromosome 6 with growth hormone deficiency: a twelve-year follow-up and literature review BMC Medical Genetics ·Stefano Stagi, Elisabetta Lapi, Maria A. Pantaleo, Massimo Carella, Antonio Petracca, Agostina De Crescenzo, Leopoldo Zelante, Andrea Riccio, Maurizio de Martino	2015	16
20	Triple X syndrome and puberty: focus on the hypothalamus-hypophysis-gonad axis Fertility and Sterility ·Stefano Stagi, Mariarosaria Di Tommaso, Perla Scalini, Elisabetta Lapi, Stefania Losi, Erica Bencini, Fabrizio Masoni, Laura Dosa, Sabrina Becciani, Maurizio de Martino	2016	15

About Elisabetta Lapi

Elisabetta Lapi is a scholar working on Developmental Biology, Developmental Neuroscience, Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 48 papers that have together received 957 indexed citations. Recurring topics across this work include Congenital heart defects research (9 papers), Williams Syndrome Research (7 papers), Genetic Syndromes and Imprinting (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (5 papers), Epigenetics and DNA Methylation (5 papers) and Sexual Differentiation and Disorders (4 papers). The work is most often cited by research in Developmental Biology (96 citations), Developmental Neuroscience (91 citations), Genetics (477 citations), Molecular Biology (534 citations) and Pediatrics, Perinatology and Child Health (131 citations). Elisabetta Lapi has collaborated with scholars based in Italy, Mexico and United Kingdom. Frequent co-authors include Stefano Stagi, Maurizio de Martino, Francesco Chiarelli, Salvatore Seminara, Roberto Salti, Sabrina Giglio, G. Bindi, Maria Luisa Giovannucci Uzielli, F. Majewski and Frances R. Goodman. Their work appears in journals such as HORMONES, BMC Endocrine Disorders, Clinical Endocrinology, Human Molecular Genetics and European Journal of Human Genetics.

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.

Explore authors with similar magnitude of impact