Melanie Lacaria

603 total citations
15 papers, 399 citations indexed

About

Melanie Lacaria is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Melanie Lacaria has authored 15 papers receiving a total of 399 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Genetics and 3 papers in Physiology. Recurrent topics in Melanie Lacaria's work include Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (5 papers) and Chromosomal and Genetic Variations (3 papers). Melanie Lacaria is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (5 papers) and Chromosomal and Genetic Variations (3 papers). Melanie Lacaria collaborates with scholars based in Canada, United States and Spain. Melanie Lacaria's co-authors include Wenli Gu, James R. Lupski, Ming Hong, Michael A. Rudnicki, Natasha C. Chang, Marjorie Withers, Feng Zhang, Pengfei Liu, P. J. Hastings and Jessica Segalés and has published in prestigious journals such as Cell stem cell, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Melanie Lacaria

13 papers receiving 383 citations

Peers

Countries citing papers authored by Melanie Lacaria

Since Specialization

Citations

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

Fields of papers citing papers by Melanie Lacaria

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Melanie Lacaria

This figure shows the co-authorship network connecting the top 25 collaborators of Melanie Lacaria. A scholar is included among the top collaborators of Melanie Lacaria 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 Melanie Lacaria. Melanie Lacaria is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	First case of Cayman ataxia far north of the Caribbean: A 20-year-old Inuit male with homozygous deletion in ATCAY gene 2025 ·Parkinsonism & Related Disorders ·(unknown), (unknown), Georges Maire, Maisa Yoshimoto, Melanie Lacaria, (unknown)	0
2	Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and a review of the first 3 years 2025 ·Genetics in Medicine ·Kristin D. Kernohan, (unknown), (unknown), (unknown), Melanie Lacaria, Michelle M. Axford, (unknown), (unknown), Nada Quercia, C. Anthony Rupar, (unknown), (unknown), Sharon L. Cushing, Pranesh Chakraborty	0
3	Canadian College of Medical Geneticists: clinical practice advisory document – responsibility to recontact for reinterpretation of clinical genetic testing 2024 ·Journal of Medical Genetics ·Elaine Goh, Lauren Chad, Julie Richer, Yvonne Bombard, Chloe Mighton, Ron Agatep, Melanie Lacaria, (unknown), Mary Ann Thomas, Ma’n H. Zawati, Julie MacFarlane, Anne‐Marie Laberge, Tanya N. Nelson	2
4	Ontario Newborn Screening for Spinal Muscular Atrophy: The First Year 2021 ·Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·Kristin D. Kernohan, Hugh J. McMillan, (unknown), Melanie Lacaria, (unknown), Craig Campbell, James J. Dowling, Hernán Gonorazky, Janet Marcadier, Mark A. Tarnopolsky, Jiri Vajsar, Alex MacKenzie, Pranesh Chakraborty	12
5	The Dystrophin Glycoprotein Complex Regulates the Epigenetic Activation of Muscle Stem Cell Commitment 2018 ·Cell stem cell ·Natasha C. Chang, Marie‐Claude Sincennes, Fabien Chevalier, Caroline Brun, Melanie Lacaria, Jessica Segalés, Pura Muñoz‐Cánoves, Ming Hong, Michael A. Rudnicki	102
6	Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feet 2017 ·American Journal of Medical Genetics Part A ·Melanie Lacaria, Myriam Srour, Jacques L. Michaud, Asif Doja, Elka Miller, Jeremy Schwartzentruber, (unknown), Jacek Majewski, Kym M. Boycott	15
7	A rare case of pediatric lipoma with t(9;12)(p22;q14) and evidence of HMGA2-NFIB gene fusion 2017 ·Cancer Genetics ·Melanie Lacaria, Dina El Demellawy, Jean McGowan‐Jordan	6
8	Notch Signaling Rescues Loss of Satellite Cells Lacking Pax7 and Promotes Brown Adipogenic Differentiation 2016 ·Cell Reports ·Alessandra Pasut, Natasha C. Chang, Uxía Gurriarán‐Rodríguez, (unknown), Hang Yin, Melanie Lacaria, Ming Hong, Michael A. Rudnicki	40
9	Glutamine supplementation favors weight loss in nondieting obese female patients. A pilot study 2014 ·European Journal of Clinical Nutrition ·Alessandro Laviano, Alessio Molfino, Melanie Lacaria, (unknown), Sabrina Leo, I. Preziosa, Filippo Rossi Fanelli	31
10	Circadian abnormalities in mouse models of smith–magenis syndrome: Evidence for involvement of RAI1 2013 ·American Journal of Medical Genetics Part A ·Melanie Lacaria, Wenli Gu, James R. Lupski	22
11	Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traits 2012 ·Human Molecular Genetics ·Melanie Lacaria, Corinne M. Spencer, Wenli Gu, Richard Paylor, James R. Lupski	46
12	A functional role for structural variation in metabolism 2012 ·Adipocyte ·Melanie Lacaria, Wenli Gu, James R. Lupski	1
13	A Duplication CNV That Conveys Traits Reciprocal to Metabolic Syndrome and Protects against Diet-Induced Obesity in Mice and Men 2012 ·PLoS Genetics ·Melanie Lacaria, Pradip Saha, Lorraine Potocki, Weimin Bi, Jiong Yan, Santhosh Girirajan, (unknown), Sarah H. Elsea, Katherina Walz, Lawrence Chan, James R. Lupski, Wenli Gu	36
14	Opposing phenotypes in mice with Smith–Magenis deletion and Potocki–Lupski duplication syndromes suggest gene dosage effects on fluid consumption behavior 2012 ·American Journal of Medical Genetics Part A ·Detlef Heck, Wenli Gu, Ying Cao, (unknown), Melanie Lacaria, James R. Lupski	10
15	Frequency of Nonallelic Homologous Recombination Is Correlated with Length of Homology: Evidence that Ectopic Synapsis Precedes Ectopic Crossing-Over 2011 ·The American Journal of Human Genetics ·Pengfei Liu, Melanie Lacaria, Feng Zhang, Marjorie Withers, P. J. Hastings, (unknown)	76

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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