Pedro A. Sanchez‐Lara

4.1k citations

72 papers · 2.1k indexed · 1 hit paper · h-index 24

Genetics top 2%
- Cleft Lip and Palate Research 28
- Craniofacial Disorders and Treatments 24
- Genomic variations and chromosomal abnormalities 8
- Genetics and Neurodevelopmental Disorders 5
- Genetic Syndromes and Imprinting 4
Molecular Biology top 10%
- dental development and anomalies 8
Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics 5
Surgery top 10%
- Congenital Anomalies and Fetal Surgery 5
Genetics top 10%
- Cleft Lip and Palate Research 28
- Craniofacial Disorders and Treatments 24
- Genomic variations and chromosomal abnormalities 8
- Genetics and Neurodevelopmental Disorders 5
- Genetic Syndromes and Imprinting 4

Co-authors: Nancy B. Spinner David A. Piccoli Athma A. Pai Ian D. Krantz Daniel M. Warthen Mark M. Urata Yang Chai Junichi Iwata
Cited by: Genetics Molecular Biology Pediatrics, Perinatology and Child Health
Journals: Journal of Biological Chemistry (2 papers)Journal of Clinical Investigation (1 paper)Brain (1 paper)
Partner nations: United States Italy Canada

In The Last Decade

Pedro A. Sanchez‐Lara

70 papers receiving 2.0k citations

Hit Papers

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Peers

Countries citing papers authored by Pedro A. Sanchez‐Lara

Since Specialization

Citations

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

Fields of papers citing papers by Pedro A. Sanchez‐Lara

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Pedro A. Sanchez‐Lara. 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 Pedro A. Sanchez‐Lara. The network helps show where Pedro A. Sanchez‐Lara may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Pedro A. Sanchez‐Lara, 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 Pedro A. Sanchez‐Lara Line = papers co-authored together Pedro A. Sanchez‐Lara links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Sudden Cardiac Arrest During a Sedated Cardiac Magnetic Resonance Study in a Nonsyndromic Child with Evolving Supravalvar Aortic Stenosis Due to Familial ELN Mutation Pediatric Cardiology ·Dor Markush,Pedro A. Sanchez‐Lara,Katheryn Grand,Robert Wong,Ruchira Garg	2023	2
2	The clinical spectrum of SMA‐PME and in vitro normalization of its cellular ceramide profile Annals of Clinical and Translational Neurology ·Michelle M. Lee,Graeme S. V. McDowell,Darryl C. De Vivo,Daniel Friedman,Samuel F. Berkovic,Maria Spanou,Argirios Dinopoulos,Katheryn Grand,Pedro A. Sanchez‐Lara,Michelle Allen‐Sharpley,Jodi Warman‐Chardon,Alexander Sólyom,Thierry Levade,Edward H. Schuchman,Steffany A. L. Bennett,David A. Dyment,Toni S. Pearson	2022	5
3	High prevalence of deleterious mutations in concomitant nonsyndromic cleft and outflow tract heart defects American Journal of Medical Genetics Part A ·Naikhoba C.O. Munabi,Shady Mikhail,Omar Toubat,Michelle G. Webb,Allyn Auslander,Pedro A. Sanchez‐Lara,Zarko Manojlovic,Ryan J. Schmidt,David W. Craig,William P. Magee,S. Ram Kumar	2022	5
4	Further delineation of van den Ende‐Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndrome American Journal of Medical Genetics Part A ·Clara Hildebrandt,Nisha Patel,John M. Graham,Michael J. Bamshad,Deborah A. Nickerson,Janson J. White,Colby T. Marvin,Danny E. Miller,Katheryn Grand,Pedro A. Sanchez‐Lara,Daniela N. Schweitzer,Hamad Alzaidan,Zainab Al Masseri,Fowzan S. Alkuraya,Angela E. Lin	2021	3
5	Thinking outside “The Box”: Case‐based didactics for medical education and the instructional legacy of Dr John M. Graham, Jr American Journal of Medical Genetics Part A ·Pedro A. Sanchez‐Lara,Katheryn Grand,Maria K. Haanpää,Cynthia J. Curry,Raymond Wang,Fatih Süheyl Ezgü,Catherine M. Rose,Deepika Burkardt,Robert L. Conway,Anju Relan,John C. Carey	2021	2
6	Proximal variants in CCND2 associated with microcephaly, short stature, and developmental delay: A case series and review of inverse brain growth phenotypes American Journal of Medical Genetics Part A ·Filomena Pirozzi,Benson Lee,Nicole Horsley,Deepika Burkardt,William B. Dobyns,John M. Graham,Maria Lisa Dentici,Claudia Cesario,Jens Schallner,Joseph Porrmann,Nataliya Di Donato,Pedro A. Sanchez‐Lara,Ghayda Mirzaa	2021	16
7	Congenital Heart Disease in Patients With Cleft Lip/Palate and Its Impact on Cleft Management The Cleft Palate-Craniofacial Journal ·Beina Azadgoli,Naikhoba C.O. Munabi,Artur Fahradyan,Allyn Auslander,Meghan McCullough,Nikki Aflatooni,Sally L. Davidson Ward,S. Ram Kumar,Pedro A. Sanchez‐Lara,Jordan W. Swanson,William P. Magee	2020	10
8	A Synonymous Exonic Splice Silencer Variant in IRF6 as a Novel and Cryptic Cause of Non-Syndromic Cleft Lip and Palate Genes ·Beau Sylvester,Frederick Brindopke,Akiko Suzuki,Melissa Giron,Allyn Auslander,Richard L. Maas,Becky Pinjou Tsai,Hanlin Gao,William P. Magee,Timothy C. Cox,Pedro A. Sanchez‐Lara	2020	6
9	Requirement for Jagged1-Notch2 signaling in patterning the bones of the mouse and human middle ear Scientific Reports ·Camilla Teng,Hai-Yun Yen,Lindsey Barske,Bea Smith,Juan Llamas,Neil Segil,John L. Go,Pedro A. Sanchez‐Lara,Robert E. Maxson,J. Gage Crump	2017	21
10	A Rapid and Sensitive Next-Generation Sequencing Method to Detect RB1 Mutations Improves Care for Retinoblastoma Patients and Their Families Journal of Molecular Diagnostics ·Wenhui L. Li,Jonathan D. Buckley,Pedro A. Sanchez‐Lara,Dennis T. Maglinte,Lucy Viduetsky,Tatiana V. Tatarinova,Jennifer G. Aparicio,Jonathan W. Kim,Margaret Au,Dejerianne Ostrow,Thomas C. Lee,Maurice R.G. O’Gorman,Alexander R. Judkins,David Cobrinik,Timothy J. Triche	2016	25
11	Clinical and Genomic Approaches for the Diagnosis of Craniofacial Disorders Current topics in developmental biology ·Pedro A. Sanchez‐Lara	2015	5
12	Hypertrophic scarring in cleft lip repair: a comparison of incidence among ethnic groups Clinical Epidemiology ·Cameron S. Francis,Soltani,Hammoudeh,Urata,Reinisch,Motamed,Pedro A. Sanchez‐Lara	2012	50
13	Microdeletion del(22)(q12.2) encompassing the facial development-associated gene, MN1 (meningioma 1) in a child with Pierre-Robin sequence (including cleft palate) and neurofibromatosis 2 (NF2): a case report and review of the literature BMC Medical Genetics ·Tom B. Davidson,Pedro A. Sanchez‐Lara,Linda M. Randolph,Mark D. Krieger,Shiqi Wu,Ashok Panigrahy,Hiroyuki Shimada,Anat Erdreich‐Epstein	2012	32
14	Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severity Brain ·Gisele E. Ishak,Jennifer C. Dempsey,Dennis Shaw,Hannah M. Tully,Margaret P Adam,Pedro A. Sanchez‐Lara,Ian A. Glass,Tessa Rue,Kathleen J. Millen,William B. Dobyns,Dan Doherty	2012	94
15	Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palate American Journal of Medical Genetics Part A ·Trilochan Sahoo,Aaron Theisen,Pedro A. Sanchez‐Lara,Michael Marble,Daniela N. Schweitzer,Beth S. Torchia,Allen N. Lamb,Bassem A. Bejjani,Lisa G. Shaffer,Yves Lacassie	2011	53
16	Bilateral maxillary duplication: case report and literature review Oral Surgery Oral Medicine Oral Pathology and Oral Radiology ·Ali Borzabadi‐Farahani,Stephen Yen,Dennis‐Duke Yamashita,Pedro A. Sanchez‐Lara	2011	14
17	Fetal constraint as a potential risk factor for craniosynostosis American Journal of Medical Genetics Part A ·Pedro A. Sanchez‐Lara,Suzan L. Carmichael,John M. Graham,Edward J. Lammer,Gary M. Shaw,Chen Ma,Sonja A. Rasmussen	2010	67
18	Complex management of a patient with a contiguous Xp11.4 gene deletion involving ornithine transcarbamylase: A role for detailed molecular analysis in complex presentations of classical diseases Molecular Genetics and Metabolism ·Matthew A. Deardorff,Himabindu Gaddipati,Paige Kaplan,Pedro A. Sanchez‐Lara,Neal Sondheimer,Nancy B. Spinner,Håkon Håkonarson,Can Fıçıcıoğlu,Jaya Ganesh,Thomas C. Markello,Brett Loechelt,Dina J. Zand,Marc Yudkoff,Uta Lichter‐Konecki	2008	19
19	A study of 534 fetal pathology cases from prenatal diagnosis referrals analyzed from 1989 through 2000 American Journal of Medical Genetics Part A ·Anna Laury,Pedro A. Sanchez‐Lara,Samuel H. Pepkowitz,John M. Graham	2007	13
20	NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathwaybreakdown → The American Journal of Human Genetics ·Ryan M. McDaniell,Daniel M. Warthen,Pedro A. Sanchez‐Lara,Athma A. Pai,Ian D. Krantz,David A. Piccoli,Nancy B. Spinner	2006	489

About Pedro A. Sanchez‐Lara

Pedro A. Sanchez‐Lara is a scholar working on Genetics, Rheumatology and Genetics, having authored 72 papers that have together received 2.1k indexed citations. Recurring topics across this work include Cleft Lip and Palate Research (28 papers), Craniofacial Disorders and Treatments (24 papers), Genomic variations and chromosomal abnormalities (8 papers), dental development and anomalies (8 papers), Congenital Anomalies and Fetal Surgery (5 papers), Prenatal Screening and Diagnostics (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genetic Syndromes and Imprinting (4 papers). The work is most often cited by research in Genetics (1.0k citations), Molecular Biology (939 citations) and Pediatrics, Perinatology and Child Health (244 citations). Pedro A. Sanchez‐Lara has collaborated with scholars based in United States, Italy and Canada. Frequent co-authors include Nancy B. Spinner, David A. Piccoli, Athma A. Pai, Ian D. Krantz, Daniel M. Warthen, Mark M. Urata, Yang Chai, Junichi Iwata, John M. Graham and Akiko Suzuki. Their work appears in journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Brain.

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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