Francisca Millan

3.3k citations

19 papers · 479 indexed · h-index 11

Co-authors: Kyle Retterer Elaine H. Zackai Holly Dubbs Wendy K. Chung Megan T. Cho Kenneth N. Rosenbaum Ann Nordgren Helena Malmgren
Topics: Genomics and Rare Diseases (11 papers)Genetics and Neurodevelopmental Disorders (8 papers)Genomic variations and chromosomal abnormalities (5 papers)
Cited by: Genetics Clinical Biochemistry Neurology
Journals: JAMA Nature Communications Neurology
Partner nations: United States Canada Qatar

In The Last Decade

Francisca Millan

16 papers receiving 470 citations

Peers

Countries citing papers authored by Francisca Millan

Since Specialization

Citations

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

Fields of papers citing papers by Francisca Millan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francisca Millan

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

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Systematic analysis of variants escaping nonsense-mediated decay uncovers candidate Mendelian diseases 2023 ·The American Journal of Human Genetics ·Rebecca I. Torene,María J. Guillen Sacoto,Francisca Millan,Zhancheng Zhang,(unknown),Matthew T. Oetjens,(unknown),Karen Chong,(unknown),(unknown),Inderneel Sahai,Christa Lese Martin,David H. Ledbetter,Scott M. Myers,Kevin J. Mitchell,Kyle Retterer	10
2	A recurrent de novo ATP5F1A substitution associated with neonatal complex V deficiency 2021 ·European Journal of Human Genetics ·Matthew A. Lines,Alexanne Cuillerier,Pranesh Chakraborty,Thierry Naas,(unknown),Jean Michaud,Chantal A. Pileggi,Mary‐Ellen Harper,Yan Burelle,Tomi L. Toler,Neal Sondheimer,Heather P. Crawford,Francisca Millan,Michael T. Geraghty	4
3	Haploinsufficiency of POU4F1 causes an ataxia syndrome with hypotonia and intention tremor 2021 ·Human Mutation ·Bryn D. Webb,(unknown),Thomas P. Naidich,Lynne M. Bird,Sumit Parikh,Meilín Fernández García,Lindsay B. Henderson,Francisca Millan,Yue Si,Kristen Brennand,Peter Shih-Ping Hung,Janet C. Rucker,Patricia G. Wheeler,Eric E. Schadt	0
4	Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy 2021 ·JAMA ·Andrés Moreno-De-Luca,Francisca Millan,(unknown),Houda Zghal Elloumi,Matthew T. Oetjens,(unknown),Karen E. Wain,Julie Scuffins,Scott M. Myers,Rebecca I. Torene,Vladimir G. Gainullin,Kevin J. Arvai,H. Lester Kirchner,David H. Ledbetter,Kyle Retterer,Christa Lese Martin	71
5	Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy 2021 ·Obstetrical & Gynecological Survey ·Andrés Moreno-De-Luca,Francisca Millan,(unknown),Houda Zghal Elloumi,Matthew T. Oetjens,(unknown),Karen E. Wain,Julie Scuffins,Scott M. Myers,Rebecca I. Torene,Vladimir G. Gainullin,Kevin J. Arvai,H. Lester Kirchner,David H. Ledbetter,Kyle Retterer,Christa Lese Martin	0
6	De Novo variants in EEF2 cause a neurodevelopmental disorder with benign external hydrocephalus 2020 ·Human Molecular Genetics ·(unknown),(unknown),Grace Yoon,Graeme Nimmo,Christopher M. Gómez,Michèl A.A.P. Willemsen,Francisca Millan,Alexandra Schneider,Rolph Pfundt,Arjan P.M. de Brouwer,Jonathan D. Dinman,Bert B.A. de Vries	10
7	Genetic testing of >1300 patients with cerebral palsy reveals an etiology in one-third of cases, underscoring the need for broad genetic testing and a significant recurrence risk for families. (P4.6-028) 2019 ·Neurology ·Francisca Millan,Houda Zghal Elloumi,(unknown),Julie Scuffins,Rebecca I. Torene,Dianalee McKnight	1
8	Genetic testing of >1300 patients with cerebral palsy reveals an etiology in one-third of cases, underscoring the need for broad genetic testing and a significant recurrence risk for families. (P4.6-028) 2019 ·Francisca Millan,Houda Zghal Elloumi,(unknown),Julie Scuffins,Rebecca I. Torene,Dianalee McKnight	1
9	Intellectual disability due to monoallelic variant in GATAD2B and mosaicism in unaffected parent 2018 ·American Journal of Medical Genetics Part A ·Rachel Rabin,Francisca Millan,Juan Cabrera‐Luque,John Pappas	6
10	Activating de novo mutations in NFE2L2 encoding NRF2 cause a multisystem disorder 2017 ·Nature Communications ·Peter Huppke,Susann Weißbach,Joseph A. Church,Rhonda E. Schnur,(unknown),Steffi Dreha‐Kulaczewski,W. Nikolaus Kühn‐Velten,Annika Wolf,Brenda Huppke,Francisca Millan,Amber Begtrup,(unknown),Hölger Thiele,Janine Altmüller,Peter Nürnberg,Michael Müller,Jutta Gärtner	64
11	Genotype and phenotype in 12 additional individuals with SATB2‐associated syndrome 2017 ·Clinical Genetics ·Yuri A. Zárate,Louisa Kalsner,Alice Basinger,Julie R. Jones,Chumei Li,Marta Szybowska,Zhixiang Xu,Samantha A. Schrier Vergano,Aisling R. Caffrey,(unknown),Holly Dubbs,Elaine H. Zackai,Francisca Millan,Aida Telegrafi,Berivan Baskin,Richard Person,Jennifer L. Fish,David B. Everman	28
12	EXOME SEQUENCING OFFERS A COMPREHENSIVE GENETIC EVALUATION AND HIGH DIAGNOSTIC RATE FOR ATAXIA-RELATED DISORDERS (S17.004) 2017 ·Neurology ·Francisca Millan,Dianalee McKnight,Julie Scuffins,Jane Juusola,Gabriele Richard,Amanda Lindy	0
13	A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects 2016 ·Neurogenetics ·David B. Beck,Megan T. Cho,Francisca Millan,(unknown),Mark Hannibal,Bridget O’Connor,Marwan Shinawi,Anne M. Connolly,Darrel Waggoner,Sara Halbach,Brad Angle,(unknown),Yufeng Shen,Kyle Retterer,Amber Begtrup,Renkui Bai,Wendy K. Chung	25
14	Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder 2016 ·American Journal of Medical Genetics Part A ·Francisca Millan,Megan T. Cho,Kyle Retterer,Kristin G. Monaghan,Renkui Bai,Patrik Vitazka,David B. Everman,Brooke Smith,Brad Angle,Victoria H. J. Roberts,LaDonna Immken,(unknown),Marc DiFazio,Elliott H. Sherr,Eden Haverfield,Bethany Friedman,Aida Telegrafi,Jane Juusola,Wendy K. Chung,Sherri J. Bale	42
15	De novo loss of function mutations in KIAA2022 are associated with epilepsy and neurodevelopmental delay in females 2016 ·Clinical Genetics ·(unknown),(unknown),Kyle Retterer,Francisca Millan,C. Nowak,Jessica Douglas,Ayesha Ahmad,Gerald V. Raymond,(unknown),Aurora Pujol,Amber Begtrup,Dianalee McKnight,Orrin Devinsky,Wendy K. Chung	22
16	De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia 2016 ·Journal of Medical Genetics ·Esther R. Berko,Megan T. Cho,Christine M. Eng,Yunru Shao,David A. Sweetser,Jessica L. Waxler,Nathaniel H. Robin,(unknown),Sandra Donkervoort,Payam Mohassel,Carsten G. Bönnemann,Martin G. Bialer,(unknown),Lynne A. Wolfe,Cynthia J. Tifft,Yufeng Shen,Kyle Retterer,Francisca Millan,Wendy K. Chung	44
17	De novo POGZ mutations are associated with neurodevelopmental disorders and microcephaly 2015 ·Molecular Case Studies ·Yizhou Ye,Megan T. Cho,Kyle Retterer,Nora Alexander,Tawfeg Ben‐Omran,Mariam Al‐Mureikhi,Ingrid Cristian,Patricia G. Wheeler,(unknown),Dina J. Zand,(unknown),Hilary J. Vernon,Rebecca McClellan,(unknown),Patrik Vitazka,Francisca Millan,Wendy K. Chung	39
18	Dominant Mutations in KAT6A Cause Intellectual Disability with Recognizable Syndromic Features 2015 ·The American Journal of Human Genetics ·Emma Tham,Anna Lindstrand,Avni Santani,Helena Malmgren,Addie I. Nesbitt,Holly Dubbs,Elaine H. Zackai,Michael Parker,Francisca Millan,Kenneth N. Rosenbaum,Golder N. Wilson,Ann Nordgren	87
19	Lessons from a pair of siblings with BPAN 2015 ·European Journal of Human Genetics ·Yuri A. Zárate,Julie R. Jones,Melanie A. Jones,Francisca Millan,Jane Juusola,(unknown),G. Bradley Schaefer,Michael C. Kruer	25

About Francisca Millan

Francisca Millan is a scholar working on Genetics, Psychiatry and Mental health and Genetics, having authored 19 papers that have together received 479 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (11 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genomic variations and chromosomal abnormalities (5 papers). The work is most often cited by research in Genetics (250 citations), Clinical Biochemistry (34 citations) and Neurology (35 citations). Francisca Millan has collaborated with scholars based in United States, Canada and Qatar. Frequent co-authors include Kyle Retterer, Elaine H. Zackai, Holly Dubbs, Wendy K. Chung, Megan T. Cho, Kenneth N. Rosenbaum, Ann Nordgren, Helena Malmgren, Golder N. Wilson and Michael Parker. Their work appears in journals such as JAMA, Nature Communications and Neurology.

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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