Daniel Pineda‐Alvarez

5.3k citations

45 papers · 2.2k indexed · 1 hit paper · h-index 21

Genetics top 1%
Molecular Biology top 10%
Pediatrics, Perinatology and Child Health top 2%
Surgery top 10%
Pulmonary and Respiratory Medicine top 10%

Co-authors: Benjamin D. Solomon Swaroop Aradhya Athena M. Cherry Ankita Patel Deborah Ritter Gordana Raca Sarah T. South Erik C. Thorland
Topics: Hedgehog Signaling Pathway Studies (14 papers)Genomic variations and chromosomal abnormalities (10 papers)Tracheal and airway disorders (10 papers)
Cited by: Genetics Developmental Biology Pediatrics, Perinatology and Child Health
Journals: JNCI Journal of the National Cancer Institute PEDIATRICS The American Journal of Human Genetics
Partner nations: United States Germany Colombia

In The Last Decade

Daniel Pineda‐Alvarez

42 papers receiving 2.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen)

2019 879 citations Erin Rooney Riggs, Erica Andersen et al. Genetics in Medicine profile →

Peers

Countries citing papers authored by Daniel Pineda‐Alvarez

Since Specialization

Citations

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

Fields of papers citing papers by Daniel Pineda‐Alvarez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniel Pineda‐Alvarez. 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 Daniel Pineda‐Alvarez. The network helps show where Daniel Pineda‐Alvarez may publish in the future.

Co-authorship network of co-authors of Daniel Pineda‐Alvarez

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel Pineda‐Alvarez. A scholar is included among the top collaborators of Daniel Pineda‐Alvarez 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 Daniel Pineda‐Alvarez. Daniel Pineda‐Alvarez 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	Patterns of mosaicism for sequence and copy-number variants discovered through clinical deep sequencing of disease-related genes in one million individuals 2023 ·The American Journal of Human Genetics ·Rebecca Truty,Susan Rojahn,Karen Ouyang,(unknown),Michael Kennemer,Daniel Pineda‐Alvarez,Britt Johnson,Amanda Stafford,Lina Basel‐Vanagaite,Sulagna C. Saitta,Anne Slavotinek,Settara C. Chandrasekharappa,Carlos J. Suarez,Leslie Burnett,Robert L. Nussbaum,Swaroop Aradhya	8
2	Cascade testing for hereditary cancer: comprehensive multigene panels identify unexpected actionable findings in relatives 2023 ·JNCI Journal of the National Cancer Institute ·Brandie Heald,Sara Pirzadeh‐Miller,Rachel E. Ellsworth,Sarah M. Nielsen,Emily M. Russell,Peter D. Beitsch,Edward D. Esplin,Robert L. Nussbaum,Daniel Pineda‐Alvarez,Allison W. Kurian,Heather Hampel	3
3	Carrier screening in the Mexican Jewish community using a pan-ethnic expanded carrier screening NGS panel 2021 ·Genetics in Medicine ·(unknown),(unknown),(unknown),Swaroop Aradhya,Daniel Pineda‐Alvarez,Mónica Aguinaga‐Ríos,(unknown)	4
4	Loss-of-function variants in CTNNA1 detected on multigene panel testing in individuals with gastric or breast cancer 2020 ·Genetics in Medicine ·Dana Clark,Scott T. Michalski,Rashmi Tondon,Bita Nehoray,(unknown),(unknown),Emily R. Soper,Susan M. Domchek,Anil K. Rustgi,Daniel Pineda‐Alvarez,Michael J. Anderson,Bryson W. Katona	27
5	Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen)breakdown → 2019 ·Genetics in Medicine ·Erin Rooney Riggs,Erica Andersen,Athena M. Cherry,Sibel Kantarci,Hutton M. Kearney,Ankita Patel,Gordana Raca,Deborah Ritter,Sarah T. South,Erik C. Thorland,Daniel Pineda‐Alvarez,Swaroop Aradhya,Alastair J. Martin	879
6	Noninvasive prenatal screening for aneuploidy: positive predictive values based on cytogenetic findings 2015 ·American Journal of Obstetrics and Gynecology ·Jeanne Meck,(unknown),Ludmila Matyakhina,Ayala Aviram,Carolyn Trunca,Daniel Pineda‐Alvarez,Swaroop Aradhya,Rachel T. Klein,Athena M. Cherry	41
7	Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing 2015 ·Genetics in Medicine ·Lisa R. Susswein,Megan L. Marshall,Rachel Nusbaum,Kristen J. Vogel Postula,Scott M. Weissman,(unknown),(unknown),(unknown),Jessica K. Booker,Mattia Cremona,Federica Gibellini,Patricia D. Murphy,Daniel Pineda‐Alvarez,Guido D. Pollevick,Zhixiong Xu,(unknown),Sherri J. Bale,Rachel T. Klein,Kathleen S. Hruska,Wendy K. Chung	199
8	Assessing copy number from exome sequencing and exome array CGH based on CNV spectrum in a large clinical cohort 2014 ·Genetics in Medicine ·Kyle Retterer,Julie Scuffins,Daniel Schmidt,Rachel Lewis,Daniel Pineda‐Alvarez,Amanda Stafford,Lindsay Schmidt,(unknown),Federica Gibellini,(unknown),A. D. Blair,Sherri J. Bale,Ludmila Matyakhina,Jeanne Meck,Swaroop Aradhya,Eden Haverfield	86
9	Exome Sequencing and High-Density Microarray Testing in Monozygotic Twin Pairs Discordant for Features of VACTERL Association 2012 ·Molecular Syndromology ·Benjamin D. Solomon,Daniel Pineda‐Alvarez,Donald W. Hadley,Nancy F. Hansen,(unknown),Frank X. Donovan,Settara C. Chandrasekharappa,Sung‐Kook Hong,Erich Roessler,James C. Mullikin,(unknown)	15
10	Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohort 2012 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Lucilene Arilho Ribeiro,Erich Roessler,Ping Hu,Daniel Pineda‐Alvarez,Nan Zhou,MaryPat Jones,Settara C. Chandrasekharappa,Antônio Richieri‐Costa,Maximilian Muenke	6
11	Personalized genomic medicine: Lessons from the exome 2011 ·Molecular Genetics and Metabolism ·Benjamin D. Solomon,Daniel Pineda‐Alvarez,Donald W. Hadley,NISC Comparative Sequencing Program,Jamie K. Teer,Praveen F. Cherukuri,Nancy F. Hansen,Pedro Cruz,Alice Young,Robert W. Blakesley,Brendan C. Lanpher,(unknown),Murat Sincan,Settara C. Chandrasekharappa,James C. Mullikin	11
12	De novo deletion of chromosome 20q13.33 in a patient with tracheo‐esophageal fistula, cardiac defects and genitourinary anomalies implicates GTPBP5 as a candidate gene 2011 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Benjamin D. Solomon,Daniel Pineda‐Alvarez,Donald W. Hadley,Amelia A. Keaton,Nneamaka B. Agochukwu,Manu S. Raam,Hannah Carlson-Donohoe,Aparna A. Kamat,Settara C. Chandrasekharappa	20
13	Utility of the Wender-Utah rating scale and the checklists for the diagnosis of familial attention deficit hyperactivity disorder in adults. Convergent and concurrent validities [Utilidad de la escala Wender-Utah y de las escalas de sntomas para el diagn 2010 ·Revista de Neurología ·David Pineda,Natalia Trujillo,(unknown),(unknown),(unknown),(unknown),Francisco Lopera,Daniel Pineda‐Alvarez,Mauricio Arcos‐Burgos,Maximilian Muenke	0
14	Clinical utility gene card for: Holoprosencephaly 2010 ·European Journal of Human Genetics ·Christèle Dubourg,Véronique David,Andrea Gropman,Sandra Mercier,Maximilian Muenke,Sylvie Odent,Daniel Pineda‐Alvarez,Erich Roessler	11
15	Long-term outcomes of adults with features of VACTERL association 2010 ·European Journal of Medical Genetics ·Manu S. Raam,Daniel Pineda‐Alvarez,Donald W. Hadley,Benjamin D. Solomon	38
16	Holoprosencephaly flashcards: A summary for the clinician 2010 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Benjamin D. Solomon,Daniel Pineda‐Alvarez,Sandra Mercier,Manu S. Raam,Sylvie Odent,Maximilian Muenke	13
17	Analysis of component findings in 79 patients diagnosed with VACTERL association 2010 ·American Journal of Medical Genetics Part A ·Benjamin D. Solomon,Daniel Pineda‐Alvarez,Manu S. Raam,(unknown),Amelia A. Keaton,Jorge I. Vélez,Derek A. T. Cummings	64
18	Analysis of genitourinary anomalies in patients with VACTERL (Vertebral anomalies, Anal atresia, Cardiac malformations, Tracheo‐Esophageal fistula, Renal anomalies, Limb abnormalities) association 2010 ·Congenital Anomalies ·Benjamin D. Solomon,Manu S. Raam,Daniel Pineda‐Alvarez	39
19	Compound heterozygosity for mutations in PAX6 in a patient with complex brain anomaly, neonatal diabetes mellitus, and microophthalmia 2009 ·American Journal of Medical Genetics Part A ·Benjamin D. Solomon,Daniel Pineda‐Alvarez,Joan Z. Balog,Donald W. Hadley,Andrea Gropman,R. Nandagopal,Joan C. Han,Jin S. Hahn,Delphine Blain,Brian P. Brooks,Maximilian Muenke	73
20	The mutational spectrum of holoprosencephaly-associated changes within theSHHgene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis 2009 ·Human Mutation ·Erich Roessler,Kênia Balbi El-Jaick,Christèle Dubourg,Jorge I. Vélez,Benjamin D. Solomon,Daniel Pineda‐Alvarez,Felicitas Lacbawan,Nan Zhou,Maia V. Ouspenskaia,Aimée Paulussen,Hubert Smeets,Ute Hehr,Claude Bendavid,Sherri J. Bale,Sylvie Odent,Véronique David,Maximilian Muenke	68

About Daniel Pineda‐Alvarez

Daniel Pineda‐Alvarez is a scholar working on Developmental Biology, Genetics and Genetics, having authored 45 papers that have together received 2.2k indexed citations. Recurring topics across this work include Hedgehog Signaling Pathway Studies (14 papers), Genomic variations and chromosomal abnormalities (10 papers) and Tracheal and airway disorders (10 papers). The work is most often cited by research in Genetics (1.3k citations), Developmental Biology (68 citations) and Pediatrics, Perinatology and Child Health (503 citations). Daniel Pineda‐Alvarez has collaborated with scholars based in United States, Germany and Colombia. Frequent co-authors include Benjamin D. Solomon, Swaroop Aradhya, Athena M. Cherry, Ankita Patel, Deborah Ritter, Gordana Raca, Sarah T. South, Erik C. Thorland, Hutton M. Kearney and Erin Rooney Riggs. Their work appears in journals such as JNCI Journal of the National Cancer Institute, PEDIATRICS and The American 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.

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