Melissa A. Parisi

8.6k citations

71 papers · 3.8k indexed · h-index 29

Molecular Biology top 2%
Genetics top 1%
Pediatrics, Perinatology and Child Health top 0.5%
Clinical Biochemistry top 0.5%
Surgery top 10%

Co-authors: David A. Clayton Ian A. Glass William B. Dobyns Robert P. Fisher Raj P. Kapur Phillip F. Chance Dan Doherty Baoji Xu
Topics: Genetic and Kidney Cyst Diseases (24 papers)Fetal and Pediatric Neurological Disorders (21 papers)Hedgehog Signaling Pathway Studies (13 papers)
Cited by: Clinical Biochemistry Genetics Pediatrics, Perinatology and Child Health
Journals: Nature Science Journal of Biological Chemistry
Partner nations: United States France Australia

In The Last Decade

Melissa A. Parisi

68 papers receiving 3.7k citations

Peers

Countries citing papers authored by Melissa A. Parisi

Since Specialization

Citations

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

Fields of papers citing papers by Melissa A. Parisi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Melissa A. Parisi. 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 Melissa A. Parisi. The network helps show where Melissa A. Parisi may publish in the future.

Co-authorship network of co-authors of Melissa A. Parisi

This figure shows the co-authorship network connecting the top 25 collaborators of Melissa A. Parisi. A scholar is included among the top collaborators of Melissa A. Parisi 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 Melissa A. Parisi. Melissa A. Parisi 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	Telehealth for rare disease care, research, and education across the globe: A review of the literature by the IRDiRC telehealth task force 2024 ·European Journal of Medical Genetics ·(unknown),Adam L. Hartman,(unknown),(unknown),Gareth Baynam,Lara Bloom,Marco Crimi,(unknown),Giuseppe Di Fede,Sofia Douzgou,Anneliene Hechtelt Jonker,(unknown),Friederike Mueller,James J. O’Brien,Ratna Dua Puri,(unknown),Meow‐Keong Thong,Biruté Tumiene,Melissa A. Parisi	2
2	The National Institutes of Health INvestigation of Co‐occurring conditions across the Lifespan to Understand Down syndromE (INCLUDE) Project: Accelerating research discoveries for people with Down syndrome across the lifespan 2024 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·(unknown),Huiqing Li,(unknown),Charlene Schramm,Marishka Brown,Linda Garcia,(unknown),(unknown),(unknown),(unknown),Laurie Ryan,Gail D. Pearson,Melissa A. Parisi	1
3	When is the best time to screen and evaluate for treatable genetic disorders?: A lifespan perspective 2023 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Melissa A. Parisi,Michele Caggana,Jennifer L. Cohen,Nina B. Gold,Jill A. Morris,Joseph J. Orsini,Tiina K. Urv,Melissa Wasserstein	8
4	Are we prepared to deliver gene‐targeted therapies for rare diseases? 2023 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Timothy W. Yu,Stephen F. Kingsmore,Robert C. Green,Tippi C. MacKenzie,Melissa Wasserstein,Michele Caggana,Nina B. Gold,Annie Kennedy,Priya S. Kishnani,Matthew Might,Philip J. Brooks,Jill A. Morris,Melissa A. Parisi,Tiina K. Urv	9
5	Joubert Syndrome: Ophthalmological Findings in Correlation with Genotype and Hepatorenal Disease in 99 Patients Prospectively Evaluated at a Single Center 2018 ·Ophthalmology ·Brian P. Brooks,Wadih M. Zein,A. Thompson,(unknown),Dan Doherty,Melissa A. Parisi,Ian A. Glass,May Christine V. Malicdan,Thierry Vilboux,Meghana Vemulapalli,James C. Mullikin,William A. Gahl,Meral Gunay‐Aygun	41
6	Molecular genetic findings and clinical correlations in 100 patients with Joubert syndrome and related disorders prospectively evaluated at a single center 2017 ·Genetics in Medicine ·Thierry Vilboux,Dan Doherty,Ian A. Glass,Melissa A. Parisi,Ian G. Phelps,Andrew R. Cullinane,Wadih M. Zein,Brian P. Brooks,Theo Heller,Ariane Soldatos,Neal L. Oden,(unknown),Meghana Vemulapalli,James C. Mullikin,May Christine V. Malicdan,William A. Gahl,Meral Gunay‐Aygun	88
7	Neurocognitive clinical outcome assessments for inborn errors of metabolism and other rare conditions 2016 ·Molecular Genetics and Metabolism ·Elsa Shapiro,(unknown),Heather Adams,Ann Barbier,Teresa Buracchio,Peter G. Como,Kathleen Delaney,Florian Eichler,Jonathan C. Goldsmith,(unknown),(unknown),Jonathan W. Mink,Joanne Odenkirchen,Melissa A. Parisi,Alison Skrinar,Susan E. Waisbren,Andrew E. Mulberg	26
8	DS-Connect: A Promising Tool to Improve Lives and Engage Down Syndrome Communities Worldwide 2015 ·Global Heart ·Emmanuel Peprah,Melissa A. Parisi,(unknown),(unknown),(unknown),Yvonne T. Maddox	20
9	Fanconi anemia‐like presentation in an infant with constitutional deletion of 21q including the RUNX1 gene 2011 ·American Journal of Medical Genetics Part A ·Eleanor S. Click,Barbara Cox,Susan B. Olson,Markus Grompe,Yassmine Akkari,Lisa A. Moreau,Akiko Shimamura,(unknown),Yajuan J. Liu,Kathleen A. Leppig,Dana C. Matthews,Melissa A. Parisi	15
10	We don't know what we don't study: The case for research on medication effects in pregnancy 2011 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Melissa A. Parisi,Catherine Y. Spong,Anne Zajicek,Alan E. Guttmacher	40
11	MKS3-Related Ciliopathy with Features of Autosomal Recessive Polycystic Kidney Disease, Nephronophthisis, and Joubert Syndrome 2009 ·The Journal of Pediatrics ·Meral Gunay‐Aygun,Melissa A. Parisi,Dan Doherty,M. Tuchman,Ekaterini Tsilou,David E. Kleiner,Marjan Huizing,Barış Türkbey,Peter L. Choyke,Lisa M. Guay‐Woodford,Theo Heller,Katarzyna Szymańska,Colin A. Johnson,Ian A. Glass,William A. Gahl	20
12	A Gender Assessment Team: experience with 250 patients over a period of 25 years 2007 ·Genetics in Medicine ·Melissa A. Parisi,Linda Ramsdell,Mark W. Burns,Michael C. Carr,(unknown),Daniel F. Gunther,(unknown),Elizabeth McCauley,Michael Mitchell,Kent E. Opheim,Catherine Pihoker,Gail E. Richards,Michael R. Soules,Roberta A Pagon	50
13	Variable presentation of nemaline myopathy: Novel mutation of alpha actin gene 2006 ·Muscle & Nerve ·(unknown),Melissa A. Parisi,Nigel G. Laing,Kathleen Patterson,Sídney M. Gospe	6
14	Craniofacial defects of blastogenesis: Duplication of pituitary with cleft palate and orophgaryngeal tumors 2005 ·American Journal of Medical Genetics Part A ·Anne Slavotinek,Melissa A. Parisi,Carrie L. Heike,Anne Hing,(unknown)	26
15	Multiple fetal anomalies associated with subtle subtelomeric chromosomal rearrangements 2003 ·Ultrasound in Obstetrics and Gynecology ·Vivienne Souter,Ian A. Glass,(unknown),(unknown),Melissa A. Parisi,K E Opheim,Christine M. Distèche	20
16	Molar tooth sign of the midbrain–hindbrain junction: Occurrence in multiple distinct syndromes 2003 ·American Journal of Medical Genetics Part A ·Joseph G. Gleeson,(unknown),Melissa A. Parisi,Sarah Marsh,Phillip F. Chance,Ian A. Glass,John M. Graham,Bernard L. Maria,A. James Barkovich,William B. Dobyns	160
17	Hydrocephalus and intestinal aganglionosis: Is L1CAM a modifier gene in Hirschsprung disease? 2002 ·American Journal of Medical Genetics ·Melissa A. Parisi,Raj P. Kapur,Ian R. Neilson,Robert M.W. Hofstra,(unknown),Ron C. Michaelis,Kathleen A. Leppig	39
18	Molecular genetics in pediatric dermatology 2000 ·Current Opinion in Pediatrics ·Melissa A. Parisi,Virginia P. Sybert	1
19	Outcome After Surgical Repair of Junctional Epidermolysis Bullosa–Pyloric Atresia Syndrome 1999 ·Archives of Dermatology ·(unknown),Hanna Kim,Melissa A. Parisi,Tod A. Brown,Lynne T. Smith,John H.T. Waldhausen,Virginia P. Sybert	14
20	Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathies 1991 ·Nature ·John F. Hess,Melissa A. Parisi,Jeffrey Bennett,David A. Clayton	189

About Melissa A. Parisi

Melissa A. Parisi is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Clinical Biochemistry, having authored 71 papers that have together received 3.8k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (24 papers), Fetal and Pediatric Neurological Disorders (21 papers) and Hedgehog Signaling Pathway Studies (13 papers). The work is most often cited by research in Clinical Biochemistry (486 citations), Genetics (1.7k citations) and Pediatrics, Perinatology and Child Health (1.1k citations). Melissa A. Parisi has collaborated with scholars based in United States, France and Australia. Frequent co-authors include David A. Clayton, Ian A. Glass, William B. Dobyns, Robert P. Fisher, Raj P. Kapur, Phillip F. Chance, Dan Doherty, Baoji Xu, Thomas Lisowsky and John F. Hess. Their work appears in journals such as Nature, Science and Journal of Biological Chemistry.

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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