Jennifer N. Partlow

4.0k citations

14 papers · 640 indexed · h-index 13

Molecular Biology
Genetics top 10%
Cell Biology top 10%
Cellular and Molecular Neuroscience
Pediatrics, Perinatology and Child Health

Co-authors: Christopher A. Walsh Ganeshwaran H. Mochida Brenda J. Barry A. James Barkovich R. Sean Hill Robert Hill Jillian M. Felie Lihadh Al‐Gazali
Topics: RNA modifications and cancer (4 papers)Microtubule and mitosis dynamics (3 papers)RNA Research and Splicing (3 papers)
Cited by: Cell Biology Developmental Neuroscience Genetics
Journals: Neurology Annals of Neurology The American Journal of Human Genetics
Partner nations: United States United Arab Emirates Jordan

In The Last Decade

Jennifer N. Partlow

14 papers receiving 635 citations

Peers

Countries citing papers authored by Jennifer N. Partlow

Since Specialization

Citations

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

Fields of papers citing papers by Jennifer N. Partlow

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jennifer N. Partlow. 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 Jennifer N. Partlow. The network helps show where Jennifer N. Partlow may publish in the future.

Co-authorship network of co-authors of Jennifer N. Partlow

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

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	Expanding the clinical spectrum of biallelic ZNF335 variants 2018 ·Clinical Genetics ·Katrien Stouffs,Andrew B. Stergachis,Tim Vanderhasselt,Alice Dica,Sandra Janssens,(unknown),Alexander Gheldof,Olaf A. Bodamer,Kathelijn Keymolen,Sara Seneca,I. Liebærs,Durai Jayaraman,(unknown),Jennifer N. Partlow,Christopher A. Walsh,Anna Jansen	12
2	PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic features 2018 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·(unknown),Connor Kenny,Robert Hill,Ganeshwaran H. Mochida,Ramzi Nasir,Jennifer N. Partlow,Brenda J. Barry,Muna Al‐Saffar,(unknown),Christine Stevens,Stacey Gabriel,A. James Barkovich,Jay W. Ellison,Lihadh Al‐Gazali,Christopher A. Walsh,Maria H. Chahrour	22
3	Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy 2017 ·European Journal of Medical Genetics ·Shenela Lakhani,Ryan N. Doan,Mariam Al‐Mureikhi,Jennifer N. Partlow,(unknown),Mahmoud F. Elsaid,Nada Alaaraj,A. James Barkovich,Christopher A. Walsh,Tawfeg Ben‐Omran	21
4	Deficient activity of alanyl-tRNA synthetase underlies an autosomal recessive syndrome of progressive microcephaly, hypomyelination, and epileptic encephalopathy 2017 ·Human Mutation ·Tojo Nakayama,Jiang Wu,Patricia Galvin‐Parton,(unknown),Mary R. Andriola,Robert Hill,(unknown),(unknown),Brenda J. Barry,Jennifer N. Partlow,A. James Barkovich,Jiqiang Ling,Ganeshwaran H. Mochida	46
5	Loss of PCLO function underlies pontocerebellar hypoplasia type III 2015 ·Neurology ·Momin Ahmed,Barry A. Chioza,Anna Rajab,Klaus Schmitz‐Abe,Aisha Al‐Khayat,Saeed Al-Turki,Emma L. Baple,Michael A. Patton,A. Al‐Memar,Matthew E. Hurles,Jennifer N. Partlow,Robert Hill,Gilad D. Evrony,Sarah Servattalab,Kyriacos Markianos,Christopher A. Walsh,Andrew H. Crosby,Ganeshwaran H. Mochida	41
6	Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplication 2015 ·eLife ·Andrew Kodani,Timothy W. Yu,Jeffrey R. Johnson,Divya Jayaraman,Tasha L. Johnson,Lihadh Al‐Gazali,László Sztriha,Jennifer N. Partlow,Hanjun Kim,Alexis Leigh Krup,Alexander Dammermann,Nevan J. Krogan,Christopher A. Walsh,Jeremy F. Reiter	107
7	Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humans 2013 ·Neurology ·L. Benjamin Hills,Amira Masri,(unknown),Wataru Kakegawa,Anh-Thu N. Lam,(unknown),(unknown),Robert Hill,Jennifer N. Partlow,Muna Al‐Saffar,Ramzi Nasir,Joan M. Stoler,A. James Barkovich,Masahiko Watanabe,Michisuke Yuzaki,Ganeshwaran H. Mochida	71
8	Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly 2011 ·The American Journal of Human Genetics ·Fowzan S. Alkuraya,Xuyu Cai,(unknown),Ganeshwaran H. Mochida,Mohammed S. Al‐Dosari,Jillian M. Felie,R. Sean Hill,Brenda J. Barry,Jennifer N. Partlow,Generoso G. Gascon,Amal Y. Kentab,Mohammed M. Jan,Ranad Shaheen,Yuanyi Feng,Christopher A. Walsh	2
9	Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly 2011 ·The American Journal of Human Genetics ·Fowzan S. Alkuraya,Xuyu Cai,(unknown),Ganeshwaran H. Mochida,Mohammed S. Al‐Dosari,Jillian M. Felie,R. Sean Hill,Brenda J. Barry,Jennifer N. Partlow,Generoso G. Gascon,Amal Y. Kentab,Mohammed M. Jan,Ranad Shaheen,Yuanyi Feng,Christopher A. Walsh	151
10	A Homozygous Mutation in the Tight-Junction Protein JAM3 Causes Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts 2010 ·The American Journal of Human Genetics ·Ganeshwaran H. Mochida,Vijay Ganesh,Jillian M. Felie,Danielle Gleason,R. Sean Hill,Katharine Clapham,Daniel P. Rakiec,Wen‐Hann Tan,Nadia Akawi,Muna Al‐Saffar,Jennifer N. Partlow,Sigrid Tinschert,A. James Barkovich,Bassam R. Ali,Lihadh Al‐Gazali,Christopher A. Walsh	64
11	Candidate gene sequencing of LHX2, HESX1, and SOX2 in a large schizencephaly cohort 2010 ·American Journal of Medical Genetics Part A ·Cecília Mellado,Annapurna Poduri,Danielle Gleason,Princess C. Elhosary,Brenda J. Barry,Jennifer N. Partlow,Bernard S. Chang,Gary M. Shaw,A. James Barkovich,Christopher A. Walsh	14
12	Developmental and degenerative features in a complicated spastic paraplegia 2009 ·Annals of Neurology ·M. Chiara Manzini,Anna Rajab,Thomas M. Maynard,Ganeshwaran H. Mochida,Wen‐Hann Tan,Ramzi Nasir,R. Sean Hill,Danielle Gleason,(unknown),Jennifer N. Partlow,Brenda J. Barry,(unknown),Anthony‐Samuel LaMantia,Christopher A. Walsh	27
13	The syndrome of perisylvian polymicrogyria with congenital arthrogryposis 2009 ·Brain and Development ·Annapurna Poduri,Vida Chitsazzadeh,Stefano D’Arrigo,Ermellina Fedrizzi,Chiara Pantaleoni,Daria Riva,Claudia Busse,Helmut Küster,Adre duPlessis,John Gaitanis,Mustafa Şahin,Cheryl Garganta,Meral Topçu,Kira A. Dies,Brenda J. Barry,Jennifer N. Partlow,A. James Barkovich,Christopher A. Walsh,Bernard S. Chang	13
14	Ethnically diverse causes of Walker-Warburg syndrome (WWS):FCMDmutations are a more common cause of WWS outside of the Middle East 2008 ·Human Mutation ·M. Chiara Manzini,Danielle Gleason,Bernard S. Chang,Robert Hill,Brenda J. Barry,Jennifer N. Partlow,Annapurna Poduri,Sophie Currier,Patricia Galvin‐Parton,Lawrence R. Shapiro,Karen Schmidt,Jessica G. Davis,Lina Basel‐Vanagaite,(unknown),Mustafa A. Salih,William B. Dobyns,Christopher A. Walsh	49

About Jennifer N. Partlow

Jennifer N. Partlow is a scholar working on Neurology, Genetics and Cell Biology, having authored 14 papers that have together received 640 indexed citations. Recurring topics across this work include RNA modifications and cancer (4 papers), Microtubule and mitosis dynamics (3 papers) and RNA Research and Splicing (3 papers). The work is most often cited by research in Cell Biology (186 citations), Developmental Neuroscience (45 citations) and Genetics (209 citations). Jennifer N. Partlow has collaborated with scholars based in United States, United Arab Emirates and Jordan. Frequent co-authors include Christopher A. Walsh, Ganeshwaran H. Mochida, Brenda J. Barry, A. James Barkovich, R. Sean Hill, Robert Hill, Jillian M. Felie, Lihadh Al‐Gazali, Muna Al‐Saffar and Mohammed M. Jan. Their work appears in journals such as Neurology, Annals of Neurology 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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