Jonathan Picker

4.1k citations

47 papers · 2.1k indexed · h-index 24

Impact in

Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Cognitive Neuroscience top 2%
- Autism Spectrum Disorder Research

Papers in ⓘ

Genetics 24
- Genetics and Neurodevelopmental Disorders 17
- Genomic variations and chromosomal abnormalities 15
- Genomics and Rare Diseases 7
Clinical Biochemistry 5
- Metabolism and Genetic Disorders 5

Co-authors: Amy Lawson‐Yuen (2 shared papers)Juan‐Sebastian Saldivar (1 shared paper)Steve S. Sommer (1 shared paper)Joseph T. Coyle (4 shared papers)Randi J. Hagerman (2 shared papers)Walter E. Kaufmann (2 shared papers)Elizabeth Berry‐Kravis (2 shared papers)Carol Delahunty (1 shared paper)
Journals: European Journal of Human Genetics (4 papers)PEDIATRICS (4 papers)Genetics in Medicine (3 papers)The Journal of Pediatrics (2 papers)Human Molecular Genetics (2 papers)
Partner nations: United States China Canada

In The Last Decade

Jonathan Picker

45 papers receiving 2.1k citations

Peers

Countries citing papers authored by Jonathan Picker

Since Specialization

Citations

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

Fields of papers citing papers by Jonathan Picker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 47 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Advances in the Treatment of Fragile X Syndrome PEDIATRICS ·Randi J. Hagerman, Elizabeth Berry‐Kravis, Walter E. Kaufmann, Michele Ono, Nicole Tartaglia, Ave M. Lachiewicz, Rebecca Kronk, Carol Delahunty, David Hessl, Jeannie Visootsak, Jonathan Picker, Louise W. Gane, Michael R. Tranfaglia	2008	425
2	Familial deletion within NLGN4 associated with autism and Tourette syndrome European Journal of Human Genetics ·Amy Lawson‐Yuen, Juan‐Sebastian Saldivar, Steve S. Sommer, Jonathan Picker	2008	207
3	Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes Genetics in Medicine ·Zhishuo Ou, Jonathan S. Berg, Hagith Yonath, Victoria B. Enciso, David T. Miller, Jonathan Picker, Tiffanee Lenzi, Catherine E. Keegan, V. Reid Sutton, John W. Belmont, A. Craig Chinault, James R. Lupski, Sau Wai Cheung, Elizabeth Roeder, Ankita Patel	2008	139
4	Clinical Diagnosis by Whole-Genome Sequencing of a Prenatal Sample New England Journal of Medicine ·Michael E. Talkowski, Zehra Ordulu, Vamsee Pillalamarri, Carol B. Benson, Ian Blumenthal, Susan A. Connolly, Carrie Hanscom, Naveed Hussain, Shahrin Pereira, Jonathan Picker, Jill A. Rosenfeld, Lisa G. Shaffer, Louise Wilkins‐Haug, James F. Gusella, Cynthia C. Morton	2012	119
5	Chromosomal microarray testing influences medical management Genetics in Medicine ·Michael E. Coulter, David T. Miller, David J. Harris, Pamela Hawley, Jonathan Picker, Amy E. Roberts, Magdi M. Sobeih, Mira Irons	2011	84
6	Further delineation of cardiac abnormalities in Costello syndrome American Journal of Medical Genetics ·Angela E. Lin, Paul Grossfeld, Robert M. Hamilton, Leslie Smoot, Karen W. Gripp, Virginia K. Proud, Rosanna Weksberg, Patricia G. Wheeler, Jonathan Picker, Mira Irons, Elaine H. Zackai, Bradley S. Marino, Charles I. Scott, Linda K. Nicholson	2002	78
7	An altered neonatal behavioral phenotype in Mecp2 mutant mice Neuroreport ·Jonathan Picker, Rebecca Yang, Laura Ricceri, Joanne Berger-Sweeney	2006	77
8	Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy Epilepsia ·Annapurna Poduri, Sameer S. Chopra, Edward Neilan, Princess C. Elhosary, Manju A. Kurian, Esther Meyer, Brenda J. Barry, Omar Khwaja, Mustafa A. Salih, Tommy Stödberg, Ingrid E. Scheffer, Eamonn R. Maher, Mustafa Şahin, Bai‐Lin Wu, Gerard T. Berry, Christopher A. Walsh, Jonathan Picker, Sanjeev V. Kothare	2012	68
9	Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency Stephanie Sacharow, Jonathan Picker, Harvey L. Levy	2014	67
10	Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield BMC Genomics ·Juan Geng, Jonathan Picker, Zhaojing Zheng, Xiaoqing Zhang, Jian Wang, Fuki M. Hisama, David W. Brown, Mary P. Mullen, David J. Harris, Joan M. Stoler, Ann Seman, David T. Miller, Qihua Fu, Amy E. Roberts, Yiping Shen	2014	60
11	Ube3a mRNA and protein expression are not decreased in Mecp2 mutant mice Brain Research ·Amy Lawson‐Yuen, Daniel Liu, Liqun Han, Zhichun Jiang, Guochuan Tsai, Alo C. Basu, Jonathan Picker, Jiamin Feng, Joseph T. Coyle	2007	55
12	Do Maternal Folate and Homocysteine Levels Play a Role in Neurodevelopmental Processes That Increase Risk for Schizophrenia? Harvard Review of Psychiatry ·Jonathan Picker, Joseph T. Coyle	2005	55
13	De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features Human Genetics ·Volkan Okur, Megan T. Cho, Lindsay B. Henderson, Kyle Retterer, Michael Schneider, Shannon G. Sattler, Dmitriy Niyazov, Meron Azage, Sharon E. Smith, Jonathan Picker, Sharyn A. Lincoln, Mark A. Tarnopolsky, Lauren Brady, Hans T. Björnsson, Carolyn Applegate, Amy Dameron, Rebecca Willaert, Berivan Baskin, Jane Juusola, Wendy K. Chung	2016	53
14	A novel neurodevelopmental disorder associated with compound heterozygous variants in the huntingtin gene European Journal of Human Genetics ·Lance H. Rodan, Julie S. Cohen, Ali Fatemi, Tammy Gillis, Diane Lucente, James F. Gusella, Jonathan Picker	2016	45
15	Unique bioinformatic approach and comprehensive reanalysis improve diagnostic yield of clinical exomes European Journal of Human Genetics ·Klaus Schmitz‐Abe, Qifei Li, Samantha M. Rosen, Neeharika Nori, Jill A. Madden, Casie A. Genetti, Monica H. Wojcik, Sadhana Ponnaluri, Cynthia S. Gubbels, Jonathan Picker, Anne O’Donnell‐Luria, Timothy W. Yu, Olaf A. Bodamer, Catherine A. Brownstein, Alan H. Beggs, Pankaj B. Agrawal	2019	41
16	Aberrant Drp1-mediated mitochondrial division presents in humans with variable outcomes Human Molecular Genetics ·Brittany N. Whitley, Christina Lam, Hong Cui, Katrina Haude, Renkui Bai, Luis Escobar, Afifa Hamilton, Lauren Brady, Mark A. Tarnopolsky, Lauren Dengle, Jonathan Picker, Sharyn A. Lincoln, Laura L. Lackner, Ian A. Glass, Suzanne Hoppins	2018	38
17	Arginase deficiency with lethal neonatal expression: Evidence for the glutamine hypothesis of cerebral edema The Journal of Pediatrics ·Jonathan Picker, Ana Cristina Puga, Harvey L. Levy, Deborah Marsden, Vivian E. Shih, Umberto DeGirolami, Keith L. Ligon, Stephen D. Cederbaum, Rita M. Kern, Gerald F. Cox	2003	37
18	Abnormal Mechanisms of Plasticity and Metaplasticity in Autism Spectrum Disorders and Fragile X Syndrome Journal of Child and Adolescent Psychopharmacology ·Lindsay M. Oberman, Fritz Ifert‐Miller, Umer Najib, Shahid Bashir, Joseph Gonzalez–Heydrich, Jonathan Picker, Alexander Rotenberg, Álvaro Pascual‐Leone	2016	36
19	EEG abnormalities and seizures in genetically diagnosed Fragile X syndrome International Journal of Developmental Neuroscience ·Takijah T. Heard, Sriram Ramgopal, Jonathan Picker, Sharyn A. Lincoln, Alexander Rotenberg, Sanjeev V. Kothare	2014	33
20	A recurrent 1.71 Mb genomic imbalance at 2q13 increases the risk of developmental delay and dysmorphism Clinical Genetics ·HE Yu, Karameh Hawash, Jonathan Picker, Joan M. Stoler, David K. Urion, B‐L Wu, Yiping Shen	2011	30

About Jonathan Picker

Jonathan Picker is a scholar working on Genetics, Clinical Biochemistry, Genetics, Cognitive Neuroscience and Rheumatology, having authored 47 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (17 papers), Genomic variations and chromosomal abnormalities (15 papers), Autism Spectrum Disorder Research (8 papers), Congenital heart defects research (7 papers), Genomics and Rare Diseases (7 papers), Metabolism and Genetic Disorders (5 papers), Folate and B Vitamins Research (4 papers) and Mitochondrial Function and Pathology (3 papers). The work is most often cited by research in Genetics (1.3k citations), Cognitive Neuroscience (670 citations), Clinical Biochemistry (115 citations), Molecular Biology (1.0k citations) and Pediatrics, Perinatology and Child Health (251 citations). Jonathan Picker has collaborated with scholars based in United States, China and Canada. Frequent co-authors include Amy Lawson‐Yuen, Juan‐Sebastian Saldivar, Steve S. Sommer, Joseph T. Coyle, Randi J. Hagerman, Walter E. Kaufmann, Elizabeth Berry‐Kravis, Carol Delahunty, Jeannie Visootsak and David Hessl. Their work appears in journals such as European Journal of Human Genetics, PEDIATRICS, Genetics in Medicine, The Journal of Pediatrics and Human Molecular 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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